- AAP - Section Executive Committee (2013-2015), Elected
- AAP - ListServ Working Group (2011), Chair
- North Texas Bioethics Network (2005)
- Pediatric Society of Greater Dallas (2004), Vice President, 2006; President, 2007
- Bioethics Committee, Medical City Dallas Hospital (2003-2014), Co-chair, 2007-2011; Chair, 2011-2014
- National Birth Defects Prevention Network (1998)
- Houston Bioethics Network (1997-1998)
- AAP - Section of Genetics and Birth Defects (1995)
- American College of Medical Genetics and Genomics (1995), Fellow
- American Society of Human Genetics (1990), Social Issues Committee (2000-2005)
- American Academy of Pediatrics (AAP) (1988)
Angela Scheuerle, M.D.
- Pediatrics - Genetics and Metabolism
Biography
Dr. Angela Scheuerle fell in love with genetics as a sophomore in high school and never looked back. She now has the career that she wanted at the age of 15 – even though such a profession didn’t exist at the time. Learning the intricacies of the science is like learning the secret of a magic trick. Remember the “ah hah!” moment when you suddenly mastered a two-wheeler? Genetics is like that.
Dr. Scheuerle graduated Magna Cum Laude as a biology major from Sewanee: The University of the South. She received her M.D. from The University of South Florida Morsani College of Medicine. Dr. Scheuerle completed a Pediatric Residency at Children’s Hospital Medical Center in Cincinnati, Ohio, and Medical Genetics Fellowship at Baylor College of Medicine. Her fellowship started just at the beginning of the Human Genome Project, so she got to “grow up” in genetics at a very exciting time: when it was possible to keep up with gene discoveries because it was about one every two weeks. She has also completed a fellowship in Clinical Ethics at the University of Chicago. Dr. Scheuerle is board certified in Clinical Genetics, Clinical Molecular Genetics, and Pediatrics.
She started shadowing in a craniofacial clinic during high school, where she developed a specific interest in craniofacial malformations. She has practiced Clinical Genetics in Houston and then Dallas since 1995. From 2003 to 2014 she was in private practice at Tesserae Genetics at Medical City Dallas. She has been adjunct faculty at UT Southwestern in the Program of Ethics in Science and Medicine and the Eugene McDermott Center for Human Development since 2000. She joined the Pediatric Division of Genetics and Metabolism as full faculty in September 2014. She holds secondary appointments as Professor in the McDermott Center and in the Department of Pathology, where she is also co-director of the Fellowship in Laboratory Genetics and Genomics.
In addition to clinical practice, Dr. Scheuerle does extensive work in public health and drug safety. She has worked with the Texas Department of State Health Services Birth Defects Epidemiology and Surveillance Branch since 1994. This Branch operates the Texas Birth Defect Registry, an active state surveillance system that monitors birth prevalence of congenital anomalies and genetic conditions. This has become particularly important in 2016 with the Zika virus epidemic. She is part of the birth defect surveillance group monitoring for Zika-related birth defects. In July 2016, she attended and participated in a workshop at the Centers for Disease Control and Prevention to define guidelines for evaluation and management of infants and children exposed to Zika virus.
The Birth Defects Epidemiology and Surveillance Branch also manages the Texas Center for Birth Defects Research and Prevention (TCBDRP), which performs and supports investigation into causes of birth defects. The TCBDRP participated in the 15-year, 10-state National Birth Defects Prevention Study, and Dr. Scheuerle served as the Geneticist for Texas’ contribution to that Study. She continues her involvement with research generated from both the state and national programs.
In 1997, Dr. Scheuerle joined the Antiretroviral Pregnancy Registry (APR). This is an FDA-mandated, post-marketing exposure registry that began in 1989 as the Zidovudine in Pregnancy Registry. This multi-drug registry is one of the largest of its kind, monitoring pregnancy exposure of now over 40 HIV and Hepatitis medications. Dr. Scheuerle’s role as teratologist is to identify those cases in which exposure to one or more medications temporally associates with embryopathogenesis of the anomaly. She also serves on the scientific advisory and steering committees for the APR. Her Organ System Classification schema for categorizing birth defects is one of two recommended by the FDA for use in pharmaceutical pregnancy registry work. Dr. Scheuerle now participates in other pregnancy registries and provides similar consultative services to US- and European-based pharmaceutical companies.
Dr. Scheuerle has been included in D Magazine's Best Doctors list, and was named a Super Doctor by Texas Monthly.
Education & Training
- Medical School - USF Health Morsani College of Medicine (1984-1988)
- Residency - University of Cincinnati/Children's Hospital Medical Center (1988-1991), Pediatrics
- Fellowship - Baylor College of Medicine/Texas Children's Hospital (1991-1995), Medical Genetics
Professional Associations & Affiliations
Honors & Awards
- D Magazine Best Doctor 2022-2025
- D Magazine Best Pediatric Specialist, 2004-2018, 2020-2021
- Distinguished Service Award 2010, National Birth Defect Prevention Network
- First place poster award 2009, National Birth Defect Prevention Network
- Phi Beta Kappa 1994
Books & Publications
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Books
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Appendix III: Syndromes Glossary in Cabana MD, ed. The 5-Minute Pediatric Consult. 7th ed.
Scheuerle AE. (2015), Wolters Kluwer; 1027-1033. -
Genetics in the Clinic: Clinical, Ethical and Social Implications for Primary Care.
(2001), St. Louis: Mosby -
Understanding Genetics: A Guide for Couples and Families.
(2005), Westport, CT: Greenwood Publishing. -
Clinical Genetics and Dysmorphology in Cabana M, ed. Rudolph's Pediatrics Self-Assessment and Board Review. 22nd ed.
Scheuerle A. (2014), San Francisco: McGraw Hill; 220-236. -
Review of Embryology and Clinical Genetics in Advances in Plastic Surgery.
Scheuerle A. (1998)
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Appendix III: Syndromes Glossary in Cabana MD, ed. The 5-Minute Pediatric Consult. 7th ed.
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Publications
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A Population-Based Assessment of Cancer Risk in Children With VACTERL
Tark JY, Renwick A, Tettamanti G, Harris RD, Desrosiers TA, Olshan AF, Janitz AE, Scheurer ME, Shumate CJ, Scheuerle AE, Plon SE, Huff CD, Nordgren A, Luke B, Lupo PJ, Schraw JM American Journal of Medical Genetics, Part A 2026 May 200 1004-1011 -
Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p
Wright CA, Scheuerle AE, Wilson K, García R, Koduru P Molecular Cytogenetics 2025 Dec 18 -
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder
van Oirsouw AS, Nedbalova P, Hancarova M, Prchal J, Prchalova D, Vlckova M, Bendova S, Monaghan KG, Dyer LM, Chen Y, Carere DA, te Bogt EA, Fisher H, Scheuerle AE, Riley S, Jain M, Mu W, Bodurtha JN, van Eerde AM, Stokman MF, Longo N, Balasubramanian M, Spiller M, Costain G, von der Lippe C, Tveten K, Jortveit M, Holla ØL, Isidor B, Cogné B, Glinton KE, Vuocolo B, Sierra RA, Angle B, Bontempo K, Koop K, Rabin R, Pappas J, Staffenberg DA, Joset P, Miny P, Filges I, Alali A, Vitalone K, Rosenfeld JA, Bi W, Bradbrook S, Perrier R, Ramanathan S, Gold JA, Palomares Bralo M, Ángeles Gómez-Cano M, Olney AH, Nielsen S, Ziegler A, Bonneau D, Prouteau C, Bruel AL, Caille-Benigni C, Lambert L, Yu AC, Robin NH, Goodloe D, Fischer J, Porrmann J, Hennig YD, Abou Jamra R, Herman I, Johnson IR, Hérissant L, Jouret G, van Gassen KL, van Binsbergen E, van der Zwaag B, Kamermans A, Oegema R, Sedlacek Z, Fenckova M, van Jaarsveld RH Genetics in Medicine 2025 Nov 27 -
Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report
Author Collaboration Co, Scheuerle AE, Geleske TA, Merchant N, Goldenberg PC, Vergano S, Holm IA, Jones K, Kalish J, Monteil DC, Pritchard AB, Rasmussen SA, Russell B, Santoro SL, Trapane P, Weaver KN Pediatrics 2025 Aug 156 -
Birth Defects and Adverse Pregnancy Outcomes in Hospital-based Birth Surveillance in Eswatini
Gill MM, Khumalo PN, Hoffman HJ, Chouraya C, Kunene M, Dlamini F, Tukei V, Scheuerle AE, Nhlabatsi B, Mofenson L Pediatric Infectious Disease Journal 2025 May 44 431-438 -
Maternal Diarrhea During the Periconceptional Period and the Risk of Birth Defects, National Birth Defects Prevention Study, 2006–2011
Author Collaboration tN, Waller DK, Mohan Dass NL, Oluwafemi OO, Agopian AJ, Tark JY, Hoyt AT, Scheuerle AE, Canfield MA Birth Defects Research 2025 Feb 117 -
Pharmacovigilance Pregnancy Data in a Population of Japanese Patients With Chronic Inflammatory Disease Exposed to Certolizumab Pegol
Goto M, Saito S, Scheuerle AE, Yasuda S, Houston N, Kumke T, Lauwerys B, Murashima A International Journal of Rheumatic Diseases 2025 Jan 28 -
Classification of isolated versus multiple birth defects: An automated process for population-based registries
Benjamin RH, Nguyen JM, Drummond-Borg M, Scheuerle AE, Langlois PH, Canfield MA, Shumate CJ, Mitchell LE, Agopian AJ American Journal of Medical Genetics, Part A 2024 Oct 194 -
The Antiretroviral Pregnancy Registry: Three decades of prospective monitoring for birth defects
Albano JD, Scheuerle AE, Watts DH, Beckerman KP, Mofenson LM, Pikis A, Vannappagari V, Seekins D, Cook TS, Tilson H Pharmacoepidemiology and Drug Safety 2024 Jun 33 -
Prevalence and descriptive epidemiology of choanal atresia and stenosis in Texas, 1999–2018
Benjamin RH, Marengo LK, Scheuerle AE, Agopian AJ, Mitchell LE American Journal of Medical Genetics, Part A 2024 Jun 194 -
Neonatal Encephalopathy with Hiccups and an Updated Diagnostic Approach
Chokshi RK, Cheng A, Ferrante L, Machie M, Scheuerle AE, Veltkamp D, Brion LP Pediatrics in Review 2023 Nov 24 E741-E743 -
Biallelic variants in NUDCD2 associated with a multiple malformation syndrome with cholestasis and renal failure
Scheuerle AE, Ni M, Ahmad AA, Timmons CF, Rakheja D, Gordon EE, Boothe M American Journal of Medical Genetics, Part A 2023 Sep 191 2324-2328 -
Strengthening the Evidence: Similar Rates of Neural Tube Defects Among Deliveries Regardless of Maternal HIV Status and Dolutegravir Exposure in Hospital Birth Surveillance in Eswatini
Gill MM, Khumalo P, Chouraya C, Kunene M, Dlamini F, Hoffman HJ, Scheuerle AE, Nhlabatsi B, Mngometulu W, Dlamini-Madlopha N, Mthunzi N, Mofenson L Open Forum Infectious Diseases 2023 Sep 10 -
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID American Journal of Medical Genetics, Part A 2023 Aug 191 2113-2131 -
Sunspot activity and birth defects among Texas births (1999–2016)
Hoyt AT, Shumate CJ, Langlois PH, Waller DK, Scheuerle AE, Ranjit N, Layne CS Birth Defects Research 2023 Jul 115 1120-1139 -
Patterns of co-occurring birth defects in children with anotia and microtia
Schraw JM, Benjamin RH, Shumate CJ, Canfield MA, Scott DA, McLean SD, Northrup H, Scheuerle AE, Schaaf CP, Ray JW, Chen H, Agopian AJ, Lupo PJ American Journal of Medical Genetics, Part A 2023 Mar 191 805-812 -
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
Hiatt SM, Trajkova S, Sebastiano MR, Partridge EC, Abidi FE, Anderson A, Ansar M, Antonarakis SE, Azadi A, Bachmann-Gagescu R, Bartuli A, Benech C, Berkowitz JL, Betti MJ, Brusco A, Cannon A, Caron G, Chen Y, Cochran ME, Coleman TF, Crenshaw MM, Cuisset L, Curry CJ, Darvish H, Demirdas S, Descartes M, Douglas J, Dyment DA, Elloumi HZ, Ermondi G, Faoucher M, Farrow EG, Felker SA, Fisher H, Hurst AC, Joset P, Kelly MA, Kmoch S, Leadem BR, Lyons MJ, Macchiaiolo M, Magner M, Mandrile G, Mattioli F, McEown M, Meadows SK, Medne L, Meeks NJ, Montgomery S, Napier MP, Natowicz M, Newberry KM, Niceta M, Noskova L, Nowak CB, Noyes AG, Osmond M, Prijoles EJ, Pugh J, Pullano V, Quélin C, Rahimi-Aliabadi S, Rauch A, Redon S, Reymond A, Schwager CR, Sellars EA, Scheuerle AE, Shukarova-Angelovska E, Skraban C, Stolerman E, Sullivan BR, Tartaglia M, Thiffault I, Uguen K, Umaña LA, van Bever Y, van der Crabben SN, van Slegtenhorst MA, Waisfisz Q, Washington C, Rodan LH, Myers RM, Cooper GM American Journal of Human Genetics 2023 Feb 110 215-227 -
Identifying syndromes in studies of structural birth defects: Guidance on classification and evaluation of potential impact
Benjamin RH, Mitchell LE, Scheuerle AE, Langlois PH, Canfield MA, Drummond-Borg M, Nguyen JM, Agopian AJ American Journal of Medical Genetics, Part A 2023 Jan 191 190-204 -
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation
Du H, Jolly A, Grochowski CM, Yuan B, Dawood M, Jhangiani SN, Li H, Muzny D, Fatih JM, Coban-Akdemir Z, Carlin ME, Scheuerle AE, Witzl K, Posey JE, Pendleton M, Harrington E, Juul S, Hastings PJ, Bi W, Gibbs RA, Sedlazeck FJ, Lupski JR, Carvalho CM, Liu P Genome Medicine 2022 Dec 14 -
Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol
Clowse M, Fischer-Betz R, Nelson-Piercy C, Scheuerle AE, Stephan B, Dubinsky M, Kumke T, Kasliwal R, Lauwerys B, Förger F Therapeutic Advances in Musculoskeletal Disease 2022 Apr 14 -
Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate
Sanchez ML, Benjamin RH, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scheuerle AE, Scott DA, Northrup H, Schaaf CP, Ray JW, McLean SD, Chen H, Lupo PJ, Agopian AJ Cleft Palate Craniofacial Journal 2022 Apr 59 417-426 -
Birth defect co-occurrence patterns in the Texas Birth Defects Registry
Benjamin RH, Scheuerle AE, Scott DA, Navarro Sanchez ML, Langlois PH, Canfield MA, Northrup H, Schaaf CP, Ray JW, McLean SD, Chen H, Swartz MD, Lupo PJ, Agopian AJ Pediatric Research 2022 Apr 91 1278-1285 -
Corrigendum to “Patterns of co-occurring birth defects among infants with hypospadiasˮ [J Pediatr Urol 17 (2021) 64.e1–64.e8](S1477513120306392)(10.1016/j.jpurol.2020.11.015)
Ludorf KL, Benjamin RH, Navarro Sanchez ML, McLean SD, Northrup H, Mitchell LE, Langlois PH, Canfield MA, Scheuerle AE, Scott DA, Schaaf CP, Ray JW, Oluwafemi O, Chen H, Swartz MD, Lupo PJ, Agopian AJ Journal of Pediatric Urology 2021 Aug 17 e1 -
Patterns of congenital anomalies among individuals with trisomy 13 in Texas
Diaz D, Benjamin RH, Navarro Sanchez ML, Mitchell LE, Langlois PH, Canfield MA, Chen H, Scheuerle AE, Schaaf CP, Scott DA, Northrup H, Ray JW, McLean SD, Swartz MD, Ludorf KL, Lupo PJ, Agopian AJ American Journal of Medical Genetics, Part A 2021 Jun 185 1787-1793 -
Asymmetric faces: Symbolic, spiritual, and representative
Scheuerle AE, Firth RM American Journal of Medical Genetics, Part C: Seminars in Medical Genetics 2021 Jun 187 278-282 -
Patterns of co-occurring birth defects among infants with hypospadias
Ludorf KL, Benjamin RH, Navarro Sanchez ML, McLean SD, Northrup H, Mitchell LE, Langlois PH, Canfield MA, Scheuerle AE, Scott DA, Schaaf CP, Ray JW, Oluwafemi O, Chen H, Swartz MD, Lupo PJ, Agopian AJ Journal of Pediatric Urology 2021 Feb 17 64.e1-64.e8 -
Risk factors and time trends for isolated craniosynostosis
Schraw JM, Woodhouse JP, Langlois PH, Canfield MA, Scheuerle AE, Agopian AJ, Benjamin RH, Lupo PJ Birth Defects Research 2021 Jan 113 43-54 -
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia
Schraw JM, Benjamin RH, Scott DA, Brooks BP, Hufnagel RB, McLean SD, Northrup H, Langlois PH, Canfield MA, Scheuerle AE, Schaaf CP, Ray JW, Chen H, Swartz MD, Mitchell LE, Agopian AJ, Lupo PJ Ophthalmic Epidemiology 2021 28 428-435 -
Birth defects that co-occur with non-syndromic gastroschisis and omphalocele
Oluwafemi OO, Benjamin RH, Navarro Sanchez ML, Scheuerle AE, Schaaf CP, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scott DA, Northrup H, Ray JW, McLean SD, Ludorf KL, Chen H, Lupo PJ, Agopian AJ American Journal of Medical Genetics, Part A 2020 Nov 182 2581-2593 -
Overcoming presynaptic effects of VAMP2 mutations with 4-aminopyridine treatment
Simmons RL, Li H, Alten B, Santos MS, Jiang R, Paul B, Lalani SJ, Cortesi A, Parks K, Khandelwal N, Smith-Packard B, Phoong MA, Chez M, Fisher H, Scheuerle AE, Shinawi M, Hussain SA, Kavalali ET, Sherr EH, Voglmaier SM Human mutation 2020 Nov 41 1999-2011 -
An additional case of Néstor-Guillermo progeria syndrome diagnosed in early childhood
Fisher HG, Patni N, Scheuerle AE American Journal of Medical Genetics, Part A 2020 Oct 182 2399-2402 -
Acculturation and selected birth defects among non-Hispanic Blacks in a population-based case–control study
Author Collaboration tN, Hoyt AT, Ramadhani T, Le MT, Shumate CJ, Canfield MA, Scheuerle AE Birth Defects Research 2020 Apr 112 535-554 -
Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Genetics in Medicine, (2019), 21, 12, (2755-2764), 10.1038/s41436-019-0576-0)
Blackburn AT, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, Al-Gazali L, Shamsi AM, Gomez-Ospina N, Chao HT, Mirzaa GM, Scheuerle AE, Kukolich MK, Scaglia F, Eng C, Willsey HR, Braun MC, Lamb DJ, Miller RK, Bekheirnia MR Genetics in Medicine 2020 Apr 22 821 -
Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene
Iqbal NS, Jascur TA, Harrison SM, Edwards AB, Smith LT, Choi ES, Arevalo MK, Chen C, Zhang S, Kern AJ, Scheuerle AE, Sanchez EJ, Xing C, Baker LA BMC Medical Genetics 2020 Feb 21 -
Pregnancy outcomes in the omalizumab pregnancy registry and a disease-matched comparator cohort
Namazy JA, Blais L, Andrews EB, Scheuerle AE, Cabana MD, Thorp JM, Umetsu DT, Veith JH, Sun D, Kaufman DG, Covington DL, Mukhopadhyay S, Fogel RB, Lopez-Leon S, Spain CV Journal of Allergy and Clinical Immunology 2020 Feb 145 528-536.e1 -
Health care supervision for children with Williams syndrome
Author Collaboration CO, Morris CA, Braddock SR, Chen E, Trotter TL, Berry SA, Burke LW, Geleske TA, Hamid R, Hopkin RJ, Introne WJ, Lyons MJ, Scheuerle AE, Stoler JM, Freedenberg DL, Jones MC, Saul RA, Tarini BA Pediatrics 2020 Feb 145 -
Clinical exome studies have inconsistent coverage
Gotway G, Crossley E, Kozlitina J, Xing C, Fan J, Hornbuckle C, Thies J, Michel D, Quinn C, Scheuerle AE, Umana LA, Uhles CL, Park JY Clinical chemistry 2020 Jan 66 199-206 -
Defect evaluation by infant photographs in a multicenter pharmaceutical clinical trial
Scheuerle AE, Kwon P, Joing M Birth Defects Research 2020 Jan 112 118-121 -
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract
Blackburn AT, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, Gazali LA, Mohamed Saeed Mohamed Al Shamsi A, Gomez-Ospina N, Chao HT, Mirzaa GM, Scheuerle AE, Kukolich MK, Scaglia F, Eng C, Willsey HR, Braun MC, Lamb DJ, Miller RK, Bekheirnia MR Genetics in Medicine 2019 Dec 21 2755-2764 -
Likelihood of meeting defined VATER/VACTERL phenotype in infants with esophageal atresia with or without tracheoesophageal fistula
Guptha S, Shumate C, Scheuerle AE American Journal of Medical Genetics, Part A 2019 Nov 179 2202-2206 -
Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries
Benjamin RH, Yu X, Navarro Sanchez ML, Chen H, Mitchell LE, Langlois PH, Canfield MA, Swartz MD, Scheuerle AE, Scott DA, Northrup H, Schaaf CP, Ray JW, McLean SD, Lupo PJ, Agopian AJ Birth Defects Research 2019 Nov 111 1356-1364 -
Levetiracetam Pregnancy Registry: Final results and a review of the impact of registry methodology and definitions on the prevalence of major congenital malformations
Scheuerle AE, Holmes LB, Albano JD, Badalamenti V, Battino D, Covington D, Harden C, Miller D, Montouris GD, Pantaleoni C, Thorp J, Tofighy A, Tomson T, Golembesky AK Birth Defects Research 2019 Aug 111 872-887 -
Association between Birth Defects and Cancer Risk among Children and Adolescents in a Population-Based Assessment of 10 Million Live Births
Lupo PJ, Schraw JM, Desrosiers TA, Nembhard WN, Langlois PH, Canfield MA, Copeland G, Meyer RE, Brown AL, Chambers TM, Sok P, Danysh HE, Carozza SE, Sisoudiya SD, Hilsenbeck SG, Janitz AE, Oster ME, Scheuerle AE, Schiffman JD, Luo C, Mian A, Mueller BA, Huff CD, Rasmussen SA, Scheurer ME, Plon SE JAMA Oncology 2019 Aug 5 1150-1158 -
Incontinentia pigmenti in adults
Scheuerle AE American Journal of Medical Genetics, Part A 2019 Aug 179 1415-1419 -
Sociodemographic, health behavioral, and clinical risk factors for anotia/microtia in a population-based case-control study
Author Collaboration NB, Ryan MA, Olshan AF, Canfield MA, Hoyt AT, Scheuerle AE, Carmichael SL, Shaw GM, Werler MM, Fisher SC, Desrosiers TA International Journal of Pediatric Otorhinolaryngology 2019 Jul 122 18-26 -
Temporal trends in diagnoses of congenital microcephaly, Texas Hospital Discharge Diagnoses, 2000–2015
Waller DK, Tark JY, Agopian AJ, Shewale J, Ganduglia-Cazaban C, Hoyt AT, Scheuerle AE, Langlois PH Birth Defects Research 2019 Jun 111 584-590 -
Selected acculturation factors and birth defects in the National Birth Defects Prevention Study, 1997–2011
Author Collaboration tN, Hoyt AT, Shumate CJ, Canfield MA, Le M, Ramadhani T, Scheuerle AE Birth Defects Research 2019 Jun 111 598-612 -
Health supervision for children with neurofibromatosis type 1
Author Collaboration CO, Miller DT, Freedenberg D, Schorry E, Ullrich NJ, Viskochil D, Korf BR, Chen E, Trotter TL, Berry SA, Burke LW, Geleske TA, Hamid R, Hopkin RJ, Introne WJ, Lyons MJ, Scheuerle AE, Stoler JM Pediatrics 2019 May 143 -
An additional case of Hennekam lymphangiectasia–lymphedema syndrome caused by loss-of-function mutation in ADAMTS3
Scheuerle A, Sweed NT, Timmons CF, Smith ED, Alcaraz WA, Shinde DN American Journal of Medical Genetics, Part A 2018 Dec 176 2858-2861 -
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation
Wooderchak-Donahue WL, Johnson P, McDonald J, Blei F, Berenstein A, Sorscher M, Mayer J, Scheuerle AE, Lewis T, Grimmer JF, Richter GT, Steeves MA, Lin AE, Stevenson DA, Bayrak-Toydemir P European Journal of Human Genetics 2018 Oct 26 1521-1536 -
Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy
Nguyen TT, Murakami Y, Wigby KM, Baratang NV, Rousseau J, St-Denis A, Rosenfeld JA, Laniewski SC, Jones J, Iglesias AD, Jones MC, Masser-Frye D, Scheuerle AE, Perry DL, Taft RJ, Le Deist F, Thompson M, Kinoshita T, Campeau PM American Journal of Human Genetics 2018 Oct 103 602-611 -
Pregnancy Outcomes After Exposure to Certolizumab Pegol: Updated Results From a Pharmacovigilance Safety Database
Clowse ME, Scheuerle AE, Chambers C, Afzali A, Kimball AB, Cush JJ, Cooney M, Shaughnessy L, Vanderkelen M, Förger F Arthritis and Rheumatology 2018 Sep 70 1399-1407 -
Pre-Zika descriptive epidemiology of microcephaly in Texas, 2008–2012
Hoyt AT, Canfield MA, Langlois PH, Waller DK, Agopian AJ, Shumate CJ, Hall NB, Marengo LK, Ethen MK, Scheuerle AE Birth Defects Research 2018 Mar 110 395-405 -
Some Intensification and Refining
Scheuerle AE Journal of Craniofacial Surgery 2017 Jan -
Enamel pit defects and taurodontism in a patient with ring chromosome 14 and 47,XXX
Townsend JA, Lacour L, Scheuerle AE Journal of Dentistry for Children 2017 Jan 84 39-43 -
Birth defects and neonatal morbidity caused by teratogen exposure after the embryonic period
Scheuerle AE, Aylsworth AS Birth Defects Research Part A - Clinical and Molecular Teratology 2016 Nov 106 935-939 -
Update: Interim guidance for the evaluation and management of infants with possible congenital Zika virus infection — United States, August 2016
Author Collaboration EV, Russell K, Oliver SE, Lewis L, Barfield WD, Cragan J, Meaney-Delman D, Staples JE, Fischer M, Peacock G, Oduyebo T, Petersen EE, Zaki S, Moore CA, Rasmussen SA, Agus M, Bailey DB, Bale J, Beckmann KA, Bhatia J, Pitre JB, Brei TJ, Daniel-Robinson L, Gaffney M, Dziuban E, Griffin DD, Goodman AB, Hall M, Phillips Heine R, Houtrow A, Hunter L, Hyman SL, Jones WK, Kapogiannis BG, Lehman SS, Lopata A, Maldonado Y, McCabe E, McLeod R, Meek JY, Msall ME, Mofenson LM, Nayak S, Needle S, Reef S, Rice S, Rivkees S, Rodriguez J, Sanchez P, Sanchez P, Scheuerle A Morbidity and Mortality Weekly Report 2016 Aug 65 870-878 -
Mandibulofacial dysostosis with microcephaly: Mutation and database update
Author Collaboration CC, Author Collaboration UC, Huang L, Vanstone MR, Hartley T, Osmond M, Barrowman N, Allanson J, Baker L, Dabir TA, Dipple KM, Dobyns WB, Estrella J, Faghfoury H, Favaro FP, Goel H, Gregersen PA, Gripp KW, Grix A, Guion-Almeida ML, Harr MH, Hudson C, Hunter AG, Johnson J, Joss SK, Kimball A, Kini U, Kline AD, Lauzon J, Lildballe DL, López-González V, Martinezmoles J, Meldrum C, Mirzaa GM, Morel CF, Morton JE, Pyle LC, Quintero-Rivera F, Richer J, Scheuerle AE, Schönewolf-Greulich B, Shears DJ, Silver J, Smith AC, Temple IK, van de Kamp JM, van Dijk FS, Vandersteen AM, White SM, Zackai EH, Zou R, Bulman DE Human mutation 2016 Feb 37 148-154 -
Prenatal exposure to zidovudine and risk for ventricular septal defects and congenital heart defects: Data from the Antiretroviral Pregnancy Registry
Vannappagari V, Albano JD, Koram N, Tilson H, Scheuerle AE, Napier MD European Journal of Obstetrics and Gynecology and Reproductive Biology 2016 Feb 197 6-10 -
Maternal occupational exposure to polycyclic aromatic hydrocarbons and craniosynostosis among offspring in the national birth defects prevention study
Author Collaboration NB, O'Brien JL, Langlois PH, Lawson CC, Scheuerle A, Rocheleau CM, Waters MA, Symanski E, Romitti PA, Agopian AJ, Lupo PJ Birth Defects Research Part A - Clinical and Molecular Teratology 2016 Jan 106 55-60 -
Population-Based Birth Defects Data in the United States, 2008 to 2012: Presentation of State-Specific Data and Descriptive Brief on Variability of Prevalence
Author Collaboration ft, Mai CT, Isenburg J, Langlois PH, Alverson CJ, Gilboa SM, Rickard R, Canfield MA, Anjohrin SB, Lupo PJ, Jackson DR, Stallings EB, Scheuerle AE, Kirby RS Birth Defects Research Part A - Clinical and Molecular Teratology 2015 Nov 103 972-993 -
Descriptive Epidemiology of Birth Defects Thought to Arise by New Mutation
Langlois PH, Scheuerle AE Birth Defects Research Part A - Clinical and Molecular Teratology 2015 Nov 103 913-927 -
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation
Rojnueangnit K, Xie J, Gomes A, Sharp A, Callens T, Chen Y, Liu Y, Cochran M, Abbott MA, Atkin J, Babovic-Vuksanovic D, Barnett CP, Crenshaw M, Bartholomew DW, Basel L, Bellus G, Ben-Shachar S, Bialer MG, Bick D, Blumberg B, Cortes F, David KL, Destree A, Duat-Rodriguez A, Earl D, Escobar L, Eswara M, Ezquieta B, Frayling IM, Frydman M, Gardner K, Gripp KW, Hernández-Chico C, Heyrman K, Ibrahim J, Janssens S, Keena BA, Llano-Rivas I, Leppig K, Mcdonald M, Misra VK, Mulbury J, Narayanan V, Orenstein N, Galvin-Parton P, Pedro H, Pivnick EK, Powell CM, Randolph L, Raskin S, Rosell J, Rubin K, Seashore M, Schaaf CP, Scheuerle A, Schultz M, Schorry E, Schnur R, Siqveland E, Tkachuk A, Tonsgard J, Upadhyaya M, Verma IC, Wallace S, Williams C, Zackai E, Zonana J, Lazaro C, Claes K, Korf B, Martin Y, Legius E, Messiaen L Human mutation 2015 Nov 36 1052-1063 -
Expanding the Molecular and Clinical Phenotype of SSR4-CDG
Author Collaboration Uo, Ng BG, Raymond K, Kircher M, Buckingham KJ, Wood T, Shendure J, Nickerson DA, Bamshad MJ, Wong JT, Monteiro FP, Graham BH, Jackson S, Sparkes R, Scheuerle AE, Cathey S, Kok F, Gibson JB, Freeze HH Human mutation 2015 Nov 36 1048-1051 -
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay
Chong JX, McMillin MJ, Shively KM, Beck AE, Marvin CT, Armenteros JR, Buckingham KJ, Nkinsi NT, Boyle EA, Berry MN, Bocian M, Foulds N, Uzielli ML, Haldeman-Englert C, Hennekam RC, Kaplan P, Kline AD, Mercer CL, Nowaczyk MJ, Klein Wassink-Ruiter JS, McPherson EW, Moreno RA, Scheuerle AE, Shashi V, Stevens CA, Carey JC, Monteil A, Lory P, Tabor HK, Smith JD, Shendure J, Nickerson DA, Bamshad MJ American Journal of Human Genetics 2015 Mar 96 462-473 -
The Xolair Pregnancy Registry (EXPECT): The safety of omalizumab use during pregnancy
Namazy J, Cabana MD, Scheuerle AE, Thorp JM, Chen H, Carrigan G, Wang Y, Veith J, Andrews EB Journal of Allergy and Clinical Immunology 2015 Feb 135 407-412 -
Sociodemographic and hispanic acculturation factors and isolated anotia/microtia
Author Collaboration NB, Hoyt AT, Canfield MA, Shaw GM, Waller DK, Polen KN, Ramadhani T, Anderka MT, Scheuerle AE Birth Defects Research Part A - Clinical and Molecular Teratology 2014 Nov 100 852-862 -
Birth Defects, Causal Attributions, and Ethnicity in the National Birth Defects Prevention Study
Case AP, Royle M, Scheuerle AE, Carmichael SL, Moffitt K, Ramadhani T Journal of Genetic Counseling 2014 Oct 23 860-873 -
A modified panel of sentinel congenital anomalies for potential use in mutation epidemiology based on birth defects registry data
Langlois PH, Moffitt KB, Scheuerle AE American Journal of Medical Genetics, Part A 2014 Sep 164 2187-2199 -
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea
Xia F, Bainbridge MN, Tan TY, Wangler MF, Scheuerle AE, Zackai EH, Harr MH, Sutton VR, Nalam RL, Zhu W, Nash M, Ryan MM, Yaplito-Lee J, Hunter JV, Deardorff MA, Penney SJ, Beaudet AL, Plon SE, Boerwinkle EA, Lupski JR, Eng CM, Muzny DM, Yang Y, Gibbs RA American Journal of Human Genetics 2014 May 94 784-789 -
Mortality in babies with achondroplasia: Revisited
Simmons K, Hashmi SS, Scheuerle A, Canfield M, Hecht JT Birth Defects Research Part A - Clinical and Molecular Teratology 2014 Apr 100 247-249 -
Insight into IKBKG/NEMO locus: Report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease
Conte MI, Pescatore A, Paciolla M, Esposito E, Miano MG, Lioi MB, Mcaleer MA, Giardino G, Pignata C, Irvine AD, Scheuerle AE, Royer G, Hadj-Rabia S, Bodemer C, Bonnefont JP, Munnich A, Smahi A, Steffann J, Fusco F, Ursini MV Human mutation 2014 Feb 35 165-177 -
The childless man
Scheuerle AE, Picconi JL, Neidich J, Panny S, Plecher BA, Randolph LM, Trapane P, Trotter TL American Journal of Medical Genetics, Part A 2014 Feb 164 561 -
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Kaiser FJ, Ansari M, Braunholz D, Gil-Rodríguez MC, Decroos C, Wilde JJ, Fincher CT, Kaur M, Bando M, Amor DJ, Atwal PS, Bahlo M, Bowman CM, Bradley JJ, Brunner HG, Clark D, Campo MD, Di Donato N, Diakumis P, Dubbs H, Dyment DA, Eckhold J, Ernst S, Ferreira JC, Francey LJ, Gehlken U, Guillén-Navarro E, Gyftodimou Y, Hall BD, Hennekam R, Hudgins L, Hullings M, Hunter JM, Yntema H, Innes AM, Kline AD, Krumina Z, Lee H, Leppig K, Lynch SA, Mallozzi MB, Mannini L, Mckee S, Mehta SG, Micule I, Consortium CR, Mohammed S, Moran E, Mortier GR, Moser JA, Noon SE, Nozaki N, Nunes L, Pappas JG, Penney LS, Pérez-Aytés A, Petersen MB, Puisac B, Revencu N, Roeder E, Saitta S, Scheuerle AE, Schindeler KL, Siu VM, Stark Z, Strom SP, Thiese H, Vater I, Willems P, Williamson K, Wilson LC, Hakonarson H, Quintero-Rivera F, Wierzba J, Musio A, Gillessen-Kaesbach G, Ramos FJ, Jackson LG, Shirahige K, Pié J, Christianson DW, Krantz ID, Fitzpatrick DR, Deardorff MA Human molecular genetics 2014 23 2888-2900 -
Final results from the Betaseron (interferon β-1b) Pregnancy Registry: A prospective observational study of birth defects and pregnancy-related adverse events
Coyle PK, Sinclair SM, Scheuerle AE, Thorp JM, Albano JD, Rametta MJ BMJ Open 2014 4 -
Response to Mariani Et al.: A second report of PARK2 duplication and developmental delay
Scheuerle AE, Wilson KS American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 2013 Jul 162 484 -
Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions
Schaaf CP, Boone PM, Sampath S, Williams C, Bader PI, Mueller JM, Shchelochkov OA, Brown CW, Crawford HP, Phalen JA, Tartaglia NR, Evans P, Campbell WM, Chun-Hui Tsai A, Parsley L, Grayson SW, Scheuerle A, Luzzi CD, Thomas SK, Eng PA, Kang SH, Patel A, Stankiewicz P, Cheung SW European Journal of Human Genetics 2012 Dec 20 1240-1247 -
Association of microtia with maternal nutrition
Ma C, Shaw GM, Scheuerle AE, Canfield MA, Carmichael SL Birth Defects Research Part A - Clinical and Molecular Teratology 2012 Dec 94 1026-1032 -
Prenatal diagnosis and cesarean section in a large, population-based birth defects registry
Case AP, Colpitts LR, Langlois PH, Scheuerle AE Journal of Maternal-Fetal and Neonatal Medicine 2012 Apr 25 395-402 -
Descriptive epidemiology of selected heritable birth defects in Texas
Moffitt KB, Abiri OO, Scheuerle AE, Langlois PH Birth Defects Research Part A - Clinical and Molecular Teratology 2011 Dec 91 990-994 -
Do foreign- and U.S.-born mothers across racial/ethnic groups have a similar risk profile for selected sociodemographic and periconceptional factors?
Ramadhani TA, Canfield MA, Farag NH, Royle M, Correa A, Waller DK, Scheuerle A Birth Defects Research Part A - Clinical and Molecular Teratology 2011 Sep 91 823-830 -
Maternal use of hot tub and major structural birth defects
Duong HT, Shahrukh Hashmi S, Ramadhani T, Canfield MA, Scheuerle A, Kim Waller D Birth Defects Research Part A - Clinical and Molecular Teratology 2011 Sep 91 836-841 -
Investigation into an increase in plagiocephaly in Texas from 1999 to 2007
Sheu SU, Ethen MK, Scheuerle AE, Langlois PH Archives of Pediatrics and Adolescent Medicine 2011 Aug 165 708-713 -
Distinctive genetic and clinical features of CMT4J: A severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4
Nicholson G, Lenk GM, Reddel SW, Grant AE, Towne CF, Ferguson CJ, Simpson E, Scheuerle A, Yasick M, Hoffman S, Blouin R, Brandt C, Coppola G, Biesecker LG, Batish SD, Meisler MH Brain 2011 Jul 134 1959-1971 -
PARK2 copy number aberrations in two children presenting with autism spectrum disorder: Further support of an association and possible evidence for a new microdeletion/microduplication syndrome
Scheuerle A, Wilson K American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 2011 Jun 156 413-420 -
Clinical differentiation of patent foramen ovale and secundum atrial septal defect: a survey of pediatric cardiologists in Dallas, Texas, USA.
Scheuerle A Journal of registry management 2011 Mar 38 4-8 -
Birth defects among a cohort of infants born to HIV-infected women on antiretroviral medication
Watts DH, Huang S, Culnane M, Kaiser KA, Scheuerle A, Mofenson L, Stanley K, Newell ML, Mandelbrot L, Delfraissy JF, Cunningham CK Journal of Perinatal Medicine 2011 Mar 39 163-170 -
Association of microtia with maternal obesity and periconceptional folic acid use
Ma C, Carmichael SL, Scheuerle AE, Canfield MA, Shaw GM American Journal of Medical Genetics, Part A 2010 Nov 152 2756-2761 -
Special Editorial: Medicine's questions
Scheuerle A Journal of Craniofacial Surgery 2010 Sep 21 -
Medicine's questions.
Scheuerle A The Journal of craniofacial surgery 2010 Sep 21 -
Special Editorial: Reading genetic-speak
Scheuerle A Journal of Craniofacial Surgery 2010 Sep 21 1319-1320 -
A physician survey regarding diagnostic variability among birth defects
Langlois PH, Sheu SU, Scheuerle AE American Journal of Medical Genetics, Part A 2010 Jun 152 1594-1598 -
Occurrence of conotruncal heart birth defects in Texas: A comparison of urban/rural classifications
Langlois PH, Jandle L, Scheuerle A, Horel SA, Carozza SE Journal of Rural Health 2010 Mar 26 164-174 -
Use of oral contraceptives in pregnancy and major structural birth defects in offspring
Waller DK, Gallaway MS, Taylor LG, Ramadhani TA, Canfield MA, Scheuerle A, Hernández-Diaz S, Louik C, Correa A Epidemiology 2010 Mar 21 232-239 -
The association between use of spermicides or male condoms and major structural birth defects
Gallaway MS, Waller DK, Canfield MA, Scheuerle A Contraception 2009 Nov 80 422-429 -
Epidemiologic features and clinical subgroups of anotia/microtia in Texas
Canfield MA, Langlois PH, Nguyen LM, Scheuerle AE Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Nov 85 905-913 -
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange
Yan J, Zhang F, Brundage E, Scheuerle A, Lanpher B, Erickson RP, Powis Z, Robinson HB, Trapane PL, Stachiw-Hietpas D, Keppler-Noreuil KM, Lalani SR, Sahoo T, Chinault AC, Patel A, Cheung SW, Lupski JR Journal of medical genetics 2009 Sep 46 626-634 -
Urban versus rural residence and occurrence of septal heart defects in Texas
Langlois PH, Scheuerle A, Horel SA, Carozza SE Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Sep 85 764-772 -
Response to Charlton et al.
Scheuerle A, Vannappagari VX, Miller MK Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Sep 85 809-810 -
Are birth defects among hispanics related to maternal nativity or number of years lived in the United States?
Ramadhani T, Short V, Canfield MA, Waller DK, Correa A, Royle M, Scheuerle A Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Sep 85 755-763 -
Measurements of birth defect prevalence: Which is most useful as a comparator group for pharmaceutical pregnancy registries?
Scheuerle A, Vannappagari VX, Miller MK Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Jul 85 611-620 -
Maternal residential proximity to waste sites and industrial facilities and conotruncal heart defects in offspring
Langlois PH, Brender JD, Suarez L, Zhan FB, Mistry JH, Scheuerle A, Moody K Paediatric and Perinatal Epidemiology 2009 Jul 23 321-331 -
Qualitative descriptors of disease incidence: Commonly used and frequently muddled
Snowman C, Scheuerle A American Journal of Medical Genetics, Part A 2009 Jul 149 1460-1462 -
A case of Asian Indian OCA3 patient
Chiang PW, Spector E, Scheuerle A American Journal of Medical Genetics, Part A 2009 Jul 149 1578-1580 -
Birth defects and military service since 1990
Langlois PH, Ramadhani TA, Royle MH, Robbins JM, Scheuerle AE, Wyszynski DF Military Medicine 2009 Feb 174 170-176 -
Clinical geneticists in birth defects surveillance and epidemiology research programs: Past, present and future roles
Lin AE, Rasmussen SA, Scheuerle A, Stevenson RE Birth Defects Research Part A - Clinical and Molecular Teratology 2009 Jan 85 69-75 -
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia
Simpson MA, Scheuerle A, Hurst J, Patton MA, Stewart C, Crosby AH Clinical Genetics 2009 75 271-276 -
Alcohol consumption by women before and during pregnancy
Ethen MK, Ramadhani TA, Scheuerle AE, Canfield MA, Wyszynski DF, Druschel CM, Romitti PA Maternal and child health journal 2009 13 274-285 -
The prevalence and predictors of anencephaly and spina bifida in Texas
Canfield MA, Marengo L, Ramadhani TA, Suarez L, Brender JD, Scheuerle A Paediatric and Perinatal Epidemiology 2009 Jan 23 41-50 -
Teenager with uterine didelphys, absent kidney and 22q11.2 deletion
Scheuerle A American Journal of Medical Genetics, Part A 2008 Mar 146 800-801 -
Residential proximity to waste sites and industrial facilities and chromosomal anomalies in offspring
Brender JD, Zhan FB, Langlois PH, Suarez L, Scheuerle A International Journal of Hygiene and Environmental Health 2008 Mar 211 50-58 -
Diagnosis, counseling, and gender assignment [1]
Scheuerle A Genetics in Medicine 2007 Dec 9 856 -
Using registry data to suggest which birth defects may be more susceptible to artifactual clusters and trends
Langlois PH, Scheuerle A Birth Defects Research Part A - Clinical and Molecular Teratology 2007 Nov 79 798-805 -
Antiepileptic drug exposure and major congenital malformations: The role of pregnancy registries
Tomson T, Battino D, French J, Harden C, Holmes L, Morrow J, Robert-Gnansia E, Scheuerle A, Vajda F, Wide K, Gordon J Epilepsy and Behavior 2007 Nov 11 277-282 -
Variable co-diagnosis of plagiocephaly and torticollis in Texas health care facilities
Pivar SJ, Scheuerle A Journal of Craniofacial Surgery 2006 Mar 17 236-240 -
Complete trisomy 1q with mosaic Y;1 translocation: A recurrent aneuploidy presenting diagnostic dilemmas
Scheuerle A, Heller K, Elder F American Journal of Medical Genetics 2005 Oct 138 A 166-170 -
The high school reunion model of medical professionalism
Scheuerle A Journal of Craniofacial Surgery 2005 Sep 16 747-748 -
UNDERSTANDING GENETICS: A Primer for Couples and Families
Scheuerle A 2005 Jan -
Assessing the risk of birth defects associated with antiretroviral exposure during pregnancy
Heather Watts D, Covington DL, Beckerman K, Garcia P, Scheuerle A, Dominguez K, Ross B, Sacks S, Chavers S, Tilson H American journal of obstetrics and gynecology 2004 Sep 191 985-992 -
Clinical review procedures for the Antiretroviral Pregnancy Registry
Scheuerle A, Covington D Pharmacoepidemiology and Drug Safety 2004 Aug 13 529-536 -
Re: fgfr2 mutations among thai children with crouzon and apert syndromes.
Scheuerle A Journal of Craniofacial Surgery 2003 Jan 14 98 -
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism
Scaglia F, Scheuerle AE, Towbin JA, Armstrong DL, Sweetman L, Wong LJ BMC Pediatrics 2002 Dec 2 -
Birth defect classification by organ system: A novel approach to heighten teratogenic signalling in a pregnancy registry
Scheuerle A, Tilson H Pharmacoepidemiology and Drug Safety 2002 Sep 11 465-475 -
Sex ratios in infants with congenital anomalies [4]
Waller DK, Keddie AM, Canfield MA, Scheuerle AE Teratology 2002 66 60 -
Good practice eliminates dilemmas
Scheuerle A American Journal of Bioethics 2001 Mar 1 2 -
Do infants with major congenital anomalies have an excess of macrosomia?
Waller DK, Keddie AM, Canfield MA, Scheuerle AE Teratology 2001 64 311-317 -
Limits of the genetic revolution
Scheuerle A Archives of Pediatrics and Adolescent Medicine 2001 155 1204-1209 -
Genetic origins of disease
Scheuerle A Journal of Craniofacial Surgery 2001 12 105-108 -
Ethics and craniofacial surgery
Scheuerle A Journal of Craniofacial Surgery 2000 Feb 11 3-9 -
Frequency of prenatal diagnosis of birth defects in Houston, Galveston and the Lower Rio Grande Valley, Texas 1995
Waller DK, Pujazon MA, Canfield MA, Scheuerle AE, Byrne JL Fetal Diagnosis and Therapy 2000 Jan 15 348-354 -
Clarification of a diagnosis of IP [2] (multiple letters)
Roberts JL, Scheuerle A American Journal of Medical Genetics 1999 85 426 -
Commentary on Hallermann-Streiff syndrome: Experience with 15 patients and review of the literature
Scheuerle A Journal of Craniofacial Surgery 1999 10 225 -
A defect by many other names
Scheuerle A Journal of Craniofacial Surgery 1998 Oct 9 415-416 -
Male cases of incontinentia pigmenti: Case report and review
Scheuerle AE American Journal of Medical Genetics 1998 May 77 201-218 -
Update in craniofacial genetics
Scheuerle AE Journal of Craniofacial Surgery 1997 8 244-245 -
Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti Type 2
Parrish JE, Scheuerle AE, Lewis RA, Levy ML, Nelson DL Human molecular genetics 1996 Nov 5 1777-1783 -
Heterogeneity of Cerebral Palsy
Scheuerle AE Archives of Pediatrics and Adolescent Medicine 1996 Apr 150 443 -
Macroglossia: More than meets the eye [4]
Scheuerle AE Journal of Pediatrics 1996 128 865 -
Recent advances in craniofacial genetics
Scheuerle AE Journal of Craniofacial Surgery 1995 Nov 6 440-442 -
Dysmorphic features in patients with complex glycerol kinase deficiency
Scheuerle A, Greenberg F, McCabe ER The Journal of pediatrics 1995 May 126 764-767 -
Adrenal crisis in the newborn: Details leading to the correct diagnosis
Vogiatzi MG, Gunn SK, Scheuerle AE, McCabe ER, Copeland KC Journal of Clinical Endocrinology and Metabolism 1995 Apr 80 1079-1082 -
Gonadal mosaicism for incontinentia pigmenti in a healthy male
Kirchman TT, Levy ML, Lewis RA, Kanzler MH, Nelson DL, Scheuerle AE Journal of medical genetics 1995 32 887-890 -
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter→Xq26.1::15p11→15qter)
Scheuerle A, Zenger-Hain JL, Van Dyke DL, Ledbetter DH, Greenberg F, Shaffer LG American Journal of Medical Genetics 1995 56 403-408 -
Facilitating diagnosis, prognosis, and management: Distinguishing isolated and syndromic anomalies
Scheuerle A Journal of Craniofacial Surgery 1994 Sep 5 208-212 -
De novo mutation in three families with multigenerational incontinentia pigmenti [1]
Scheuerle A, Lewis RA, Levy ML, Nelson DL American Journal of Human Genetics 1994 55 1279-1281 -
Arginase deficiency presenting as cerebral palsy
Scheuerle AE, McVie R, Beaudet AL, Shapira SK Pediatrics 1993 Jan 91 995-996 -
Involvement of the thymus and cellular immune system in craniofacial malformation syndromes
Scheuerle AE, Good RA, Habal MB Journal of Craniofacial Surgery 1990 Apr 1 88-90
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A Population-Based Assessment of Cancer Risk in Children With VACTERL
Research
- Teratogenic risks of prescription medication/drug safety
- Syndrome definition
- Public health genetics and birth defect surveillance
Children's Medical Center of Dallas
1935 Medical District DriveDallas, Texas 75235 214-730-5437 Directions to Children's Medical Center of Dallas at Children's Medical Center of Dallas, Dallas