| Year |
Citation |
Score |
| 2024 |
Benjamin RH, Nguyen JM, Drummond-Borg M, Scheuerle AE, Langlois PH, Canfield MA, Shumate CJ, Mitchell LE, Agopian AJ. Classification of isolated versus multiple birth defects: An automated process for population-based registries. American Journal of Medical Genetics. Part A. e63714. PMID 38770996 DOI: 10.1002/ajmg.a.63714 |
0.618 |
|
| 2024 |
Benjamin RH, Marengo LK, Scheuerle AE, Agopian AJ, Mitchell LE. Prevalence and descriptive epidemiology of choanal atresia and stenosis in Texas, 1999-2018. American Journal of Medical Genetics. Part A. e63549. PMID 38314656 DOI: 10.1002/ajmg.a.63549 |
0.64 |
|
| 2022 |
Swanson J, Shumate C, Agopian AJ, Mitchell LE, Canfield MA, Salemi JL. Factors associated with Medicaid participation among infants born with birth defects in Texas, 2010-2014. Birth Defects Research. 114: 895-905. PMID 37702980 DOI: 10.1002/bdr2.2077 |
0.623 |
|
| 2022 |
Benjamin RH, Mitchell LE, Scheuerle AE, Langlois PH, Canfield MA, Drummond-Borg M, Nguyen JM, Agopian AJ. Identifying syndromes in studies of structural birth defects: Guidance on classification and evaluation of potential impact. American Journal of Medical Genetics. Part A. PMID 36286533 DOI: 10.1002/ajmg.a.63014 |
0.606 |
|
| 2022 |
Mitchell LE. Maternal genetic factors in the development of congenital heart defects. Current Opinion in Genetics & Development. 76: 101961. PMID 35882070 DOI: 10.1016/j.gde.2022.101961 |
0.371 |
|
| 2022 |
Musfee FI, Oluwafemi OO, Agopian AJ, Hakonarson H, Goldmuntz E, Mitchell LE. Maternal effect genes as risk factors for congenital heart defects. Hgg Advances. 3: 100098. PMID 35345810 DOI: 10.1016/j.xhgg.2022.100098 |
0.656 |
|
| 2022 |
Woodward AA, Taylor DM, Goldmuntz E, Mitchell LE, Agopian AJ, Moore JH, Urbanowicz RJ. Gene-Interaction-Sensitive enrichment analysis in congenital heart disease. Biodata Mining. 15: 4. PMID 35151364 DOI: 10.1186/s13040-022-00287-w |
0.553 |
|
| 2022 |
Mitchell LE. Maternal effect genes: Update and review of evidence for a link with birth defects. Hgg Advances. 3: 100067. PMID 35047854 DOI: 10.1016/j.xhgg.2021.100067 |
0.33 |
|
| 2021 |
Oluwafemi OO, Musfee FI, Mitchell LE, Goldmuntz E, Xie HM, Hakonarson H, Morrow BE, Guo T, Taylor DM, McDonald-McGinn DM, Emanuel BS, Agopian AJ. Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes. 12. PMID 34356046 DOI: 10.3390/genes12071030 |
0.578 |
|
| 2021 |
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, et al. Corrigendum to "Patterns of co-occurring birth defects among infants with hypospadiasˮ [J Pediatr Urol 17 (2021) 64.e1-64.e8]. Journal of Pediatric Urology. PMID 34325994 DOI: 10.1016/j.jpurol.2021.07.008 |
0.567 |
|
| 2021 |
Musfee FI, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Taylor DM, Tristani-Firouzi M, Watkins WS, Yandell M, Mitchell LE. Common Variation in Cytoskeletal Genes is Associated with Conotruncal Heart Defects. Genes. 12. PMID 33925651 DOI: 10.3390/genes12050655 |
0.604 |
|
| 2021 |
Sanchez MLN, 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. Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 10556656211010060. PMID 33906455 DOI: 10.1177/10556656211010060 |
0.597 |
|
| 2021 |
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, et al. Patterns of congenital anomalies among individuals with trisomy 13 in Texas. American Journal of Medical Genetics. Part A. PMID 33749998 DOI: 10.1002/ajmg.a.62175 |
0.638 |
|
| 2020 |
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, et al. A COMPREHENSIVE ASSESSMENT OF CO-OCCURRING BIRTH DEFECTS AMONG INFANTS WITH NON-SYNDROMIC ANOPHTHALMIA OR MICROPHTHALMIA. Ophthalmic Epidemiology. 1-8. PMID 33345678 DOI: 10.1080/09286586.2020.1862244 |
0.612 |
|
| 2020 |
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, et al. Patterns of co-occurring birth defects among infants with hypospadias. Journal of Pediatric Urology. PMID 33281045 DOI: 10.1016/j.jpurol.2020.11.015 |
0.602 |
|
| 2020 |
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, et al. Birth defects that co-occur with non-syndromic gastroschisis and omphalocele. American Journal of Medical Genetics. Part A. PMID 32885608 DOI: 10.1002/Ajmg.A.61830 |
0.649 |
|
| 2020 |
Lei Y, Ludorf KL, Yu X, Benjamin RH, Gu X, Lin Y, Finnell RH, Mitchell LE, Musfee FI, Malik S, Canfield MA, Morrison AC, Hobbs CA, Van Zutphen AR, Fisher S, et al. Maternal hypertension-related genotypes and congenital heart defects. American Journal of Hypertension. PMID 32710738 DOI: 10.1093/Ajh/Hpaa116 |
0.659 |
|
| 2020 |
Sewda A, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Musfee F, Taylor D, Mitchell LE. Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects. Plos One. 15: e0234357. PMID 32516339 DOI: 10.1371/Journal.Pone.0234357 |
0.664 |
|
| 2019 |
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, ... ... Mitchell LE, et al. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics. PMID 31870554 DOI: 10.1016/J.Ajhg.2019.11.010 |
0.611 |
|
| 2019 |
Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE. X-chromosome association studies of congenital heart defects. American Journal of Medical Genetics. Part A. PMID 31729158 DOI: 10.1002/Ajmg.A.61411 |
0.604 |
|
| 2019 |
Lupo PJ, Mitchell LE, Jenkins MM. Genome-wide association studies of structural birth defects: A review and commentary. Birth Defects Research. PMID 31654503 DOI: 10.1002/Bdr2.1606 |
0.435 |
|
| 2019 |
Benjamin RH, Lopez A, Mitchell LE, Tsao K, Johnson A, Langlois PH, Swartz MD, Agopian AJ. Mortality by mode of delivery among infants with spina bifida in Texas. Birth Defects Research. PMID 31642615 DOI: 10.1002/Bdr2.1608 |
0.58 |
|
| 2019 |
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society For Cardiovascular Magnetic Resonance. 21: 51. PMID 31422771 DOI: 10.1186/S12968-019-0555-2 |
0.577 |
|
| 2019 |
Sewda A, Agopian AJ, Goldmuntz E, Hakonarson H, Morrow BE, Taylor D, Mitchell LE. Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects. Plos One. 14: e0219926. PMID 31314787 DOI: 10.1371/Journal.Pone.0219926 |
0.644 |
|
| 2019 |
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, et al. Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registries. Birth Defects Research. PMID 31313535 DOI: 10.1002/Bdr2.1549 |
0.629 |
|
| 2019 |
Kaplinski M, Taylor D, Mitchell LE, Hammond DA, Goldmuntz E, Agopian AJ. The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect. Plos One. 14: e0216477. PMID 31141530 DOI: 10.1371/Journal.Pone.0216477 |
0.658 |
|
| 2019 |
Lopez A, Benjamin RH, Raut JR, Ramakrishnan A, Mitchell LE, Tsao K, Johnson A, Langlois PH, Swartz MD, Agopian AJ. Mode of delivery and mortality among neonates with gastroschisis: A population-based cohort in Texas. Paediatric and Perinatal Epidemiology. PMID 31087678 DOI: 10.1111/Ppe.12554 |
0.573 |
|
| 2019 |
Hoang TT, Lei Y, Mitchell LE, Sharma SV, Swartz MD, Waller DK, Finnell RH, Benjamin RH, Browne ML, Canfield MA, Lupo PJ, McKenzie P, Shaw GM, Agopian AJ. Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspring. Molecular Genetics & Genomic Medicine. e688. PMID 30968606 DOI: 10.1002/Mgg3.688 |
0.667 |
|
| 2019 |
Benjamin RH, Littlejohn S, Canfield MA, Ethen MK, Hua F, Mitchell LE. Interpregnancy change in body mass index and infant outcomes in Texas: a population-based study. Bmc Pregnancy and Childbirth. 19: 119. PMID 30953457 DOI: 10.1186/S12884-019-2265-Z |
0.335 |
|
| 2019 |
Hoang TT, Lei Y, Mitchell LE, Sharma SV, Swartz MD, Waller DK, Finnell RH, Benjamin RH, Browne ML, Canfield MA, Lupo PJ, McKenzie P, Shaw G, Agopian AJ. Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study. The Journal of Nutrition. PMID 30689919 DOI: 10.1093/Jn/Nxy246 |
0.658 |
|
| 2019 |
Kousa YA, Zhu H, Fakhouri WD, Lei Y, Kinoshita A, Roushangar RR, Patel NK, Agopian AJ, Yang W, Leslie EJ, Busch TD, Mansour TA, Li X, Smith AL, Li EB, ... ... Mitchell LE, et al. The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Human Molecular Genetics. PMID 30689861 DOI: 10.1093/Hmg/Ddz010 |
0.615 |
|
| 2019 |
Shewale JB, Ganduglia Cazaban CM, Waller DK, Mitchell LE, Langlois PH, Agopian AJ. Microcephaly inpatient hospitalization and potential Zika outbreak in Texas: A cost and predicted economic burden analysis. Travel Medicine and Infectious Disease. PMID 30639780 DOI: 10.1016/J.Tmaid.2019.01.001 |
0.519 |
|
| 2018 |
Benjamin RH, Mitchell LE, Canfield MA, Hoyt AT, Lai D, Ramadhani TA, Carmichael SL, Case AP, Waller DK. Fish consumption prior to pregnancy and pregnancy outcomes in the National Birth Defects Prevention Study, 1997-2011. Public Health Nutrition. 1-8. PMID 30326983 DOI: 10.1017/S1368980018002641 |
0.353 |
|
| 2018 |
Benjamin RH, Littlejohn S, Mitchell LE. Bariatric surgery and birth defects: A systematic literature review. Paediatric and Perinatal Epidemiology. PMID 30307630 DOI: 10.1111/Ppe.12517 |
0.384 |
|
| 2018 |
Chambers TM, Agopian AJ, Lewis RA, Langlois PH, Danysh HE, Weber KA, Shaw GM, Mitchell LE, Lupo PJ. Epidemiology of anophthalmia and microphthalmia: Prevalence and patterns in Texas, 1999-2009. American Journal of Medical Genetics. Part A. PMID 30070760 DOI: 10.1002/Ajmg.A.40352 |
0.679 |
|
| 2018 |
Van Horne BS, Caughy MO, Canfield M, Case AP, Greeley CS, Morgan R, Mitchell LE. First-time maltreatment in children ages 2-10 with and without specific birth defects: A population-based study. Child Abuse & Neglect. 84: 53-63. PMID 30053644 DOI: 10.1016/J.Chiabu.2018.07.003 |
0.718 |
|
| 2018 |
Hoang TT, Goldmuntz E, Roberts AE, Chung WK, Kline JK, Deanfield JE, Giardini A, Aleman A, Gelb BD, Mac Neal M, Porter GA, Kim R, Brueckner M, Lifton RP, Edman S, ... ... Mitchell LE, et al. The Congenital Heart Disease Genetic Network Study: Cohort description. Plos One. 13: e0191319. PMID 29351346 DOI: 10.1371/Journal.Pone.0191319 |
0.629 |
|
| 2017 |
J Lupo P, Agopian AJ, Castillo H, Castillo J, Clayton GH, Dosa NP, Hopson B, Joseph DB, Rocque BG, Walker WO, Wiener JS, Mitchell LE. Genetic epidemiology of neural tube defects. Journal of Pediatric Rehabilitation Medicine. PMID 29125517 DOI: 10.3233/Prm-170456 |
0.628 |
|
| 2017 |
Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, ... ... Mitchell LE, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/Circgenetics.116.001690 |
0.591 |
|
| 2017 |
Hoang TT, Agopian AJ, Mitchell LE. Maternal Use of Weight Loss Products and the Risk of Neural Tube Defects in Offspring: A Systematic Literature Review. Birth Defects Research. PMID 29024488 DOI: 10.1002/Bdr2.1116 |
0.612 |
|
| 2017 |
Kim J, Swartz MD, Langlois PH, Romitti PA, Weyer P, Mitchell LE, Luben TJ, Ramakrishnan A, Malik S, Lupo PJ, Feldkamp ML, Meyer RE, Winston JJ, Reefhuis J, Blossom SJ, et al. Estimated Maternal Pesticide Exposure from Drinking Water and Heart Defects in Offspring. International Journal of Environmental Research and Public Health. 14. PMID 28786932 DOI: 10.3390/Ijerph14080889 |
0.645 |
|
| 2017 |
Kim J, Langlois PH, Mitchell LE, Agopian AJ. Maternal occupation and the risk of neural tube defects in offspring. Archives of Environmental & Occupational Health. 0. PMID 28723301 DOI: 10.1080/19338244.2017.1356259 |
0.686 |
|
| 2017 |
Hoang TT, Marengo LK, Mitchell LE, Canfield MA, Agopian AJ. Original Findings and Updated Meta-Analysis for the Association Between Maternal Diabetes and Risk for Congenital Heart Disease Phenotypes. American Journal of Epidemiology. 1-11. PMID 28505225 DOI: 10.1093/Aje/Kwx033 |
0.637 |
|
| 2017 |
Agopian AJ, Goldmuntz E, Hakonarson H, Sewda A, Taylor D, Mitchell LE. Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Circulation. Cardiovascular Genetics. 10: e001449. PMID 28468790 DOI: 10.1161/Circgenetics.116.001449 |
0.675 |
|
| 2017 |
Khokha MK, Mitchell LE, Wallingford JB. White paper on the study of birth defects. Birth Defects Research. 109: 180-185. PMID 28398650 DOI: 10.1002/Bdra.23590 |
0.446 |
|
| 2016 |
Khokha MK, Mitchell LE, Wallingford JB. An opportunity to address the genetic causes of birth defects. Pediatric Research. PMID 27925620 DOI: 10.1038/Pr.2016.229 |
0.446 |
|
| 2016 |
Agopian AJ, Hoang TT, Mitchell LE, Morrison AC, Tu D, Nassar N, Canfield MA. Maternal hypertension and risk for hypospadias in offspring. American Journal of Medical Genetics. Part A. PMID 27570224 DOI: 10.1002/Ajmg.A.37947 |
0.67 |
|
| 2015 |
Van Horne BS, Moffitt KB, Canfield MA, Case AP, Greeley CS, Morgan R, Mitchell LE. Maltreatment of Children Under Age 2 With Specific Birth Defects: A Population-Based Study. Pediatrics. PMID 26620063 DOI: 10.1542/Peds.2015-1274 |
0.697 |
|
| 2015 |
Danysh HE, Mitchell LE, Zhang K, Scheurer ME, Lupo PJ. Differences in environmental exposure assignment due to residential mobility among children with a central nervous system tumor: Texas, 1995-2009. Journal of Exposure Science & Environmental Epidemiology. PMID 26443468 DOI: 10.1038/Jes.2015.63 |
0.3 |
|
| 2015 |
Swartz MD, Cai Y, Chan W, Symanski E, Mitchell LE, Danysh HE, Langlois PH, Lupo PJ. Air toxics and birth defects: a Bayesian hierarchical approach to evaluate multiple pollutants and spina bifida. Environmental Health : a Global Access Science Source. 14: 16. PMID 25971584 DOI: 10.1186/1476-069X-14-16 |
0.392 |
|
| 2015 |
Ramakrishnan A, Lee LJ, Mitchell LE, Agopian AJ. Maternal Hypertension During Pregnancy and the Risk of Congenital Heart Defects in Offspring: A Systematic Review and Meta-analysis. Pediatric Cardiology. PMID 25951814 DOI: 10.1007/s00246-015-1182-9 |
0.625 |
|
| 2015 |
Mitchell LE, Agopian AJ, Bhalla A, Glessner JT, Kim CE, Swartz MD, Hakonarson H, Goldmuntz E. Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations. Human Molecular Genetics. 24: 265-73. PMID 25138779 DOI: 10.1093/Hmg/Ddu420 |
0.663 |
|
| 2014 |
Mitchell LE, Finnell RH. Papers from the Eighth International Neural Tube Defects Conference. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 561-2. PMID 25155952 DOI: 10.1002/Bdra.23289 |
0.302 |
|
| 2014 |
Agopian AJ, Mitchell LE, Glessner J, Bhalla AD, Sewda A, Hakonarson H, Goldmuntz E. Genome-wide association study of maternal and inherited loci for conotruncal heart defects. Plos One. 9: e96057. PMID 24800985 DOI: 10.1371/Journal.Pone.0096057 |
0.66 |
|
| 2014 |
Khodr ZG, Lupo PJ, Agopian AJ, Canfield MA, Case AP, Carmichael SL, Mitchell LE. Preconceptional folic acid-containing supplement use in the National Birth Defects Prevention Study. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 472-82. PMID 24706436 DOI: 10.1002/Bdra.23238 |
0.759 |
|
| 2014 |
Peyvandi S, Ingall E, Woyciechowski S, Garbarini J, Mitchell LE, Goldmuntz E. Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: an evaluation of 1,620 families. American Journal of Medical Genetics. Part A. 164: 1490-5. PMID 24677430 DOI: 10.1002/Ajmg.A.36500 |
0.394 |
|
| 2014 |
Lupo PJ, Mitchell LE, Canfield MA, Shaw GM, Olshan AF, Finnell RH, Zhu H. Maternal-fetal metabolic gene-gene interactions and risk of neural tube defects. Molecular Genetics and Metabolism. 111: 46-51. PMID 24332798 DOI: 10.1016/J.Ymgme.2013.11.004 |
0.387 |
|
| 2013 |
Agopian AJ, Waller DK, Lupo PJ, Canfield MA, Mitchell LE. A case-control study of maternal bathing habits and risk for birth defects in offspring. Environmental Health : a Global Access Science Source. 12: 88. PMID 24131571 DOI: 10.1186/1476-069X-12-88 |
0.697 |
|
| 2013 |
Agopian AJ, Bhalla AD, Boerwinkle E, Finnell RH, Grove ML, Hixson JE, Shimmin LC, Sewda A, Stuart C, Zhong Y, Zhu H, Mitchell LE. Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 97: 597-601. PMID 23913553 DOI: 10.1002/Bdra.23163 |
0.6 |
|
| 2013 |
Khodr ZG, Lupo PJ, Canfield MA, Chan W, Cai Y, Mitchell LE. Hispanic ethnicity and acculturation, maternal age and the risk of gastroschisis in the National Birth Defects Prevention Study. Birth Defects Research. Part a, Clinical and Molecular Teratology. 97: 538-45. PMID 23729355 DOI: 10.1002/Bdra.23140 |
0.766 |
|
| 2013 |
Zaidi S, Choi M, Wakimoto H, Ma L, Jiang J, Overton JD, Romano-Adesman A, Bjornson RD, Breitbart RE, Brown KK, Carriero NJ, Cheung YH, Deanfield J, DePalma S, Fakhro KA, ... ... Mitchell LE, et al. De novo mutations in histone-modifying genes in congenital heart disease. Nature. 498: 220-3. PMID 23665959 DOI: 10.1038/Nature12141 |
0.304 |
|
| 2013 |
Agopian AJ, Lupo PJ, Canfield MA, Mitchell LE. Swimming pool use and birth defect risk. American Journal of Obstetrics and Gynecology. 209: 219.e1-9. PMID 23628264 DOI: 10.1016/J.Ajog.2013.04.033 |
0.682 |
|
| 2013 |
Peyvandi S, Lupo PJ, Garbarini J, Woyciechowski S, Edman S, Emanuel BS, Mitchell LE, Goldmuntz E. 22q11.2 deletions in patients with conotruncal defects: Data from 1,610 consecutive cases Pediatric Cardiology. 34: 1687-1694. PMID 23604262 DOI: 10.1007/S00246-013-0694-4 |
0.369 |
|
| 2013 |
Agopian AJ, Tinker SC, Lupo PJ, Canfield MA, Mitchell LE. Proportion of neural tube defects attributable to known risk factors. Birth Defects Research. Part a, Clinical and Molecular Teratology. 97: 42-6. PMID 23427344 DOI: 10.1002/Bdra.23100 |
0.653 |
|
| 2013 |
Finnell RH, George TM, Mitchell LE. Neural Tube Defects Emery and Rimoin's Principles and Practice of Medical Genetics. 1-21. DOI: 10.1016/B978-0-12-383834-6.00120-8 |
0.417 |
|
| 2012 |
Lupo PJ, Canfield MA, Chapa C, Lu W, Agopian AJ, Mitchell LE, Shaw GM, Waller DK, Olshan AF, Finnell RH, Zhu H. Diabetes and obesity-related genes and the risk of neural tube defects in the national birth defects prevention study. American Journal of Epidemiology. 176: 1101-9. PMID 23132673 DOI: 10.1093/Aje/Kws190 |
0.659 |
|
| 2012 |
Lee LJ, Canfield MA, Hashmi SS, Moffitt KB, Marengo L, Agopian AJ, Belmont JW, Freedenberg D, Tanksley SM, Mitchell LE, Lupo PJ. Association between thyroxine levels at birth and choanal atresia or stenosis among infants in Texas, 2004-2007. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 951-4. PMID 23125093 DOI: 10.1002/Bdra.23091 |
0.624 |
|
| 2012 |
Agopian AJ, Moulik M, Gupta-Malhotra M, Marengo LK, Mitchell LE. Descriptive epidemiology of non-syndromic complete atrioventricular canal defects. Paediatric and Perinatal Epidemiology. 26: 515-24. PMID 23061687 DOI: 10.1111/Ppe.12006 |
0.657 |
|
| 2012 |
Lupo PJ, Symanski E, Langlois PH, Lawson CC, Malik S, Gilboa SM, Lee LJ, Agopian AJ, Desrosiers TA, Waters MA, Romitti PA, Correa A, Shaw GM, Mitchell LE. Maternal occupational exposure to polycyclic aromatic hydrocarbons and congenital heart defects among offspring in the national birth defects prevention study. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 875-81. PMID 22945317 DOI: 10.1002/Bdra.23071 |
0.677 |
|
| 2012 |
Agopian AJ, Eastcott LM, Mitchell LE. Age of onset and effect size in genome-wide association studies. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 908-11. PMID 22933422 DOI: 10.1002/Bdra.23066 |
0.632 |
|
| 2012 |
Etheredge AJ, Finnell RH, Carmichael SL, Lammer EJ, Zhu H, Mitchell LE, Shaw GM. Maternal and infant gene-folate interactions and the risk of neural tube defects. American Journal of Medical Genetics. Part A. 158: 2439-46. PMID 22903727 DOI: 10.1002/Ajmg.A.35552 |
0.414 |
|
| 2012 |
Agopian AJ, Lupo PJ, Herdt-Losavio ML, Langlois PH, Rocheleau CM, Mitchell LE. Differences in folic acid use, prenatal care, smoking, and drinking in early pregnancy by occupation. Preventive Medicine. 55: 341-5. PMID 22846503 DOI: 10.1016/J.Ypmed.2012.07.015 |
0.626 |
|
| 2012 |
Lupo PJ, Langlois PH, Reefhuis J, Lawson CC, Symanski E, Desrosiers TA, Khodr ZG, Agopian AJ, Waters MA, Duwe KN, Finnell RH, Mitchell LE, Moore CA, Romitti PA, Shaw GM, et al. Maternal occupational exposure to polycyclic aromatic hydrocarbons: effects on gastroschisis among offspring in the National Birth Defects Prevention Study. Environmental Health Perspectives. 120: 910-5. PMID 22330681 DOI: 10.1289/Ehp.1104305 |
0.796 |
|
| 2012 |
Agopian AJ, Lupo PJ, Tinker SC, Canfield MA, Mitchell LE. Working towards a risk prediction model for neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 141-6. PMID 22253139 DOI: 10.1002/Bdra.22883 |
0.623 |
|
| 2012 |
Agopian AJ, Canfield MA, Olney RS, Lupo PJ, Ramadhani T, Mitchell LE, Shaw GM, Moore CA. Spina bifida subtypes and sub-phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study. American Journal of Medical Genetics. Part A. 158: 109-15. PMID 22140002 DOI: 10.1002/Ajmg.A.34383 |
0.652 |
|
| 2012 |
Agopian AJ, Marengo LK, Mitchell LE. Predictors of trisomy 21 in the offspring of older and younger women. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 31-5. PMID 22125229 DOI: 10.1002/Bdra.22870 |
0.636 |
|
| 2011 |
Long J, Lupo PJ, Goldmuntz E, Mitchell LE. Evaluation of heterogeneity in the association between congenital heart defects and variants of folate metabolism genes: conotruncal and left-sided cardiac defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 879-84. PMID 21987465 DOI: 10.1002/Bdra.22849 |
0.454 |
|
| 2011 |
Weymouth KS, Blanton SH, Bamshad MJ, Beck AE, Alvarez C, Richards S, Gurnett CA, Dobbs MB, Barnes D, Mitchell LE, Hecht JT. Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. American Journal of Medical Genetics. Part A. 155: 2170-9. PMID 21834041 DOI: 10.1002/Ajmg.A.34167 |
0.35 |
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| 2011 |
Agopian AJ, Mitchell LE. MI-GWAS: a SAS platform for the analysis of inherited and maternal genetic effects in genome-wide association studies using log-linear models. Bmc Bioinformatics. 12: 117. PMID 21513519 DOI: 10.1186/1471-2105-12-117 |
0.635 |
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| 2011 |
Lupo PJ, Langlois PH, Mitchell LE. Epidemiology of Ebstein anomaly: prevalence and patterns in Texas, 1999-2005. American Journal of Medical Genetics. Part A. 155: 1007-14. PMID 21465650 DOI: 10.1002/Ajmg.A.33883 |
0.498 |
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| 2011 |
Case AP, Mitchell LE. Prevalence and patterns of choanal atresia and choanal stenosis among pregnancies in Texas, 1999-2004. American Journal of Medical Genetics. Part A. 155: 786-91. PMID 21416593 DOI: 10.1002/Ajmg.A.33882 |
0.344 |
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| 2011 |
Lupo PJ, Mitchell LE, Goldmuntz E. NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 61-5. PMID 21254360 DOI: 10.1002/Bdra.20745 |
0.485 |
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| 2011 |
Lupo PJ, Symanski E, Waller DK, Chan W, Langlois PH, Canfield MA, Mitchell LE. Maternal exposure to ambient levels of benzene and neural tube defects among offspring: Texas, 1999-2004. Environmental Health Perspectives. 119: 397-402. PMID 20923742 DOI: 10.1289/Ehp.1002212 |
0.428 |
|
| 2010 |
Long J, Ramadhani T, Mitchell LE. Epidemiology of nonsyndromic conotruncal heart defects in Texas, 1999-2004. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 971-9. PMID 20878913 DOI: 10.1002/Bdra.20724 |
0.435 |
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| 2010 |
Lupo PJ, Symanski E, Waller DK, Chan W, Canfield MA, Langlois PH, Mitchell LE. Polytomous logistic regression as a tool for exploring heterogeneity across birth defect subtypes: an example using anencephaly and spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 701-5. PMID 20740595 DOI: 10.1002/Bdra.20671 |
0.446 |
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| 2010 |
Summers CM, Mitchell LE, Stanislawska-Sachadyn A, Baido SF, Blair IA, Von Feldt JM, Whitehead AS. Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 679-88. PMID 20544798 DOI: 10.1002/Bdra.20683 |
0.34 |
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| 2010 |
Lupo PJ, Symanski E, Chan W, Mitchell LE, Waller DK, Canfield MA, Langlois PH. Differences in exposure assignment between conception and delivery: the impact of maternal mobility. Paediatric and Perinatal Epidemiology. 24: 200-8. PMID 20415777 DOI: 10.1111/J.1365-3016.2010.01096.X |
0.383 |
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| 2010 |
Lupo PJ, Goldmuntz E, Mitchell LE. Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects. Journal of Biomedicine & Biotechnology. 2010: 630940. PMID 20111745 DOI: 10.1155/2010/630940 |
0.419 |
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| 2010 |
Wen S, Zhu H, Lu W, Mitchell LE, Shaw GM, Lammer EJ, Finnell RH. Planar cell polarity pathway genes and risk for spina bifida. American Journal of Medical Genetics. Part A. 152: 299-304. PMID 20101694 DOI: 10.1002/Ajmg.A.33230 |
0.359 |
|
| 2010 |
Mitchell LE, Long J, Garbarini J, Paluru P, Goldmuntz E. Variants of folate metabolism genes and risk of left-sided cardiac defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 48-53. PMID 19777601 DOI: 10.1002/Bdra.20622 |
0.461 |
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| 2010 |
Naufal Z, Zhiwen L, Zhu L, Zhou GD, McDonald T, He LY, Mitchell L, Ren A, Zhu H, Finnell R, Donnelly KC. Biomarkers of exposure to combustion by-products in a human population in Shanxi, China. Journal of Exposure Science & Environmental Epidemiology. 20: 310-9. PMID 19277067 DOI: 10.1038/Jes.2009.19 |
0.374 |
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| 2009 |
Agopian A, Marengo L, Mitchell LE. Descriptive epidemiology of nonsyndromic omphalocele in Texas, 1999-2004. American Journal of Medical Genetics. Part A. 149: 2129-33. PMID 19760656 DOI: 10.1002/Ajmg.A.33000 |
0.648 |
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| 2009 |
Stanisławska-Sachadyn A, Mitchell LE, Woodside JV, Buckley PT, Kealey C, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women. Annals of Human Genetics. 73: 484-91. PMID 19650776 DOI: 10.1111/J.1469-1809.2009.00529.X |
0.349 |
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| 2009 |
Roessler E, Pei W, Ouspenskaia MV, Karkera JD, Veléz JI, Banerjee-Basu S, Gibney G, Lupo PJ, Mitchell LE, Towbin JA, Bowers P, Belmont JW, Goldmuntz E, Baxevanis AD, Feldman B, et al. Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly. Molecular Genetics and Metabolism. 98: 225-34. PMID 19553149 DOI: 10.1016/J.Ymgme.2009.05.005 |
0.347 |
|
| 2009 |
Hill DS, Wlodarczyk BJ, Mitchell LE, Finnell RH. Arsenate-induced maternal glucose intolerance and neural tube defects in a mouse model. Toxicology and Applied Pharmacology. 239: 29-36. PMID 19446573 DOI: 10.1016/J.Taap.2009.05.009 |
0.408 |
|
| 2008 |
Goldmuntz E, Woyciechowski S, Renstrom D, Lupo PJ, Mitchell LE. Variants of folate metabolism genes and the risk of conotruncal cardiac defects. Circulation. Cardiovascular Genetics. 1: 126-32. PMID 20031554 DOI: 10.1161/Circgenetics.108.796342 |
0.487 |
|
| 2008 |
Lu ZY, Morales M, Khartulyari S, Mei M, Murphy KM, Stanislawska-Sachadyn A, Summers CM, Huang Y, Von Feldt JM, Blair IA, Mitchell LE, Whitehead AS. Genetic and biochemical determinants of serum concentrations of monocyte chemoattractant protein-1, a potential neural tube defect risk factor. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 736-41. PMID 18937353 DOI: 10.1002/Bdra.20507 |
0.385 |
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| 2008 |
Stanisławska-Sachadyn A, Brown KS, Mitchell LE, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Human Genetics. 123: 289-95. PMID 18247058 DOI: 10.1007/S00439-008-0475-Y |
0.364 |
|
| 2008 |
Stanisławska-Sachadyn A, Woodside JV, Brown KS, Young IS, Murray L, McNulty H, Strain JJ, Boreham CA, Scott JM, Whitehead AS, Mitchell LE. Evidence for sex differences in the determinants of homocysteine concentrations. Molecular Genetics and Metabolism. 93: 355-62. PMID 18180190 DOI: 10.1016/J.Ymgme.2007.11.004 |
0.361 |
|
| 2007 |
Wen S, Ethen M, Langlois PH, Mitchell LE. Prevalence of encephalocele in Texas, 1999-2002. American Journal of Medical Genetics. Part A. 143: 2150-5. PMID 17702023 DOI: 10.1002/Ajmg.A.31907 |
0.404 |
|
| 2006 |
Jensen LE, Hoess K, Mitchell LE, Whitehead AS. Loss of function polymorphisms in NAT1 protect against spina bifida. Human Genetics. 120: 52-7. PMID 16680433 DOI: 10.1007/S00439-006-0181-6 |
0.348 |
|
| 2006 |
Jensen LE, Etheredge AJ, Brown KS, Mitchell LE, Whitehead AS. Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring. American Journal of Medical Genetics. Part A. 140: 1114-8. PMID 16596675 DOI: 10.1002/Ajmg.A.31212 |
0.356 |
|
| 2005 |
Mitchell LE, Weinberg CR. Evaluation of offspring and maternal genetic effects on disease risk using a family-based approach: the "pent" design. American Journal of Epidemiology. 162: 676-85. PMID 16093287 DOI: 10.1093/Aje/Kwi249 |
0.372 |
|
| 2005 |
Etheredge AJ, Christensen K, Del Junco D, Murray JC, Mitchell LE. Evaluation of two methods for assessing gene-environment interactions using data from the Danish case-control study of facial clefts. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 541-6. PMID 15965987 DOI: 10.1002/Bdra.20167 |
0.346 |
|
| 2005 |
Jensen LE, Hoess K, Whitehead AS, Mitchell LE. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 512-6. PMID 15959877 DOI: 10.1002/Bdra.20143 |
0.408 |
|
| 2005 |
Rampersaud E, Bassuk AG, Enterline DS, George TM, Siegel DG, Melvin EC, Aben J, Allen J, Aylsworth A, Brei T, Bodurtha J, Buran C, Floyd LE, Hammock P, Iskandar B, ... ... Mitchell LE, et al. Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. Journal of Medical Genetics. 42: 940-6. PMID 15831595 DOI: 10.1136/Jmg.2005.031658 |
0.366 |
|
| 2005 |
Mitchell LE. Epidemiology of neural tube defects. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 135: 88-94. PMID 15800877 DOI: 10.1002/Ajmg.C.30057 |
0.415 |
|
| 2004 |
Jensen LE, Barbaux S, Hoess K, Fraterman S, Whitehead AS, Mitchell LE. The human T locus and spina bifida risk. Human Genetics. 115: 475-82. PMID 15449172 DOI: 10.1007/S00439-004-1185-8 |
0.335 |
|
| 2004 |
Spiegelstein O, Mitchell LE, Merriweather MY, Wicker NJ, Zhang Q, Lammer EJ, Finnell RH. Embryonic development of folate binding protein-1 (Folbp1) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 231: 221-31. PMID 15305303 DOI: 10.1002/Dvdy.20107 |
0.304 |
|
| 2004 |
Jensen LE, Wall AM, Cook M, Hoess K, Thorn CF, Whitehead AS, Mitchell LE. A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 396-9. PMID 15211708 DOI: 10.1002/Bdra.20023 |
0.367 |
|
| 2004 |
Brown KS, Cook M, Hoess K, Whitehead AS, Mitchell LE. Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 101-6. PMID 15039923 DOI: 10.1002/Bdra.20002 |
0.396 |
|
| 2003 |
Mitchell LE, Murray JC, O'Brien S, Christensen K. Retinoic acid receptor alpha gene variants, multivitamin use, and liver intake as risk factors for oral clefts: a population-based case-control study in Denmark, 1991-1994. American Journal of Epidemiology. 158: 69-76. PMID 12835288 DOI: 10.1093/Aje/Kwg102 |
0.371 |
|
| 2003 |
Brown KS, Kluijtmans LA, Young IS, Woodside J, Yarnell JW, McMaster D, Murray L, Evans AE, Boreham CA, McNulty H, Strain JJ, Mitchell LE, Whitehead AS. Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1014-20. PMID 12689917 DOI: 10.1161/01.Atv.0000071348.70527.F4 |
0.301 |
|
| 2002 |
Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. American Journal of Human Genetics. 71: 1222-6. PMID 12375236 DOI: 10.1086/344209 |
0.42 |
|
| 2002 |
Mitchell LE, Beaty TH, Lidral AC, Munger RG, Murray JC, Saal HM, Wyszynski DF. Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 39: 93-100. PMID 11772175 DOI: 10.1597/1545-1569(2002)039<0093:GFTDAA>2.0.CO;2 |
0.302 |
|
| 2001 |
Mitchell LE, Murray JC, O'Brien S, Christensen K. Evaluation of two putative susceptibility loci for oral clefts in the Danish population. American Journal of Epidemiology. 153: 1007-15. PMID 11384957 DOI: 10.1093/Aje/153.10.1007 |
0.389 |
|
| 2000 |
Mitchell L. A common measure of disease-gene associations for case-control and tdt studies. Annals of Epidemiology. 10: 455. PMID 11018361 DOI: 10.1016/S1047-2797(00)00121-6 |
0.343 |
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| 2000 |
Mitchell LE. Relationship between case-control studies and the transmission/disequilibrium test. Genetic Epidemiology. 19: 193-201. PMID 11015123 DOI: 10.1002/1098-2272(200010)19:3<193::Aid-Gepi1>3.0.Co;2-2 |
0.329 |
|
| 2000 |
Treloar SA, Macones GA, Mitchell LE, Martin NG. Genetic influences on premature parturition in an Australian twin sample. Twin Research. 3: 80-82. DOI: 10.1375/Twin.3.2.80 |
0.368 |
|
| 1997 |
Mitchell LE. Genetic epidemiology of birth defects: Nonsyndromic cleft lip and neural tube defects Epidemiologic Reviews. 19: 61-68. PMID 9360903 DOI: 10.1093/Oxfordjournals.Epirev.A017947 |
0.371 |
|
| 1997 |
Mitchell LE. Transforming growth factor α locus and nonsyndromic cleft lip with or without cleft palate: A reappraisal Genetic Epidemiology. 14: 231-240. PMID 9181353 DOI: 10.1002/(Sici)1098-2272(1997)14:3<231::Aid-Gepi2>3.0.Co;2-8 |
0.363 |
|
| 1993 |
Mitchell LE, Risch N. Correlates of genetic risk for non-syndromic cleft lip with or without cleft palate Clinical Genetics. 43: 255-260. PMID 8375107 DOI: 10.1111/J.1399-0004.1993.Tb03813.X |
0.4 |
|
| 1993 |
Mitchell LE, Risch N. The Genetics of Infantile Hypertrophic Pyloric Stenosis: A Reanalysis American Journal of Diseases of Children. 147: 1203-1211. PMID 8237916 DOI: 10.1001/Archpedi.1993.02160350077012 |
0.318 |
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