Laura E. Mitchell - Publications

Affiliations: 
Epidemiology & Disease Control The University of Texas School of Public Health 
Area:
Public Health, Bioinformatics Biology

137 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.96
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  0.44
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  0.96
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  0.96
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  0.96
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  0.96
2019 Benjamin RH, Ethen MK, Canfield MA, Hua F, Mitchell LE. Association of interpregnancy change in body mass index and spina bifida. Birth Defects Research. PMID 31291065 DOI: 10.1002/bdr2.1547  0.44
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  0.96
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  0.96
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  0.96
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  0.44
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  0.96
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  0.96
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  0.96
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  0.44
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  0.96
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  0.32
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2016 Banfield E, Brown AL, Peckham EC, Rednam SP, Murray J, Okcu MF, Mitchell LE, Chintagumpala MM, Lau CC, Scheurer ME, Lupo PJ. Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients. Cancer Epidemiology. 44: 161-166. PMID 27607585 DOI: 10.1016/j.canep.2016.08.020  0.44
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  0.96
2016 Danysh HE, Zhang K, Mitchell LE, Scheurer ME, Lupo PJ. Maternal residential proximity to major roadways at delivery and childhood central nervous system tumors. Environmental Research. 146: 315-322. PMID 26802618 DOI: 10.1016/j.envres.2016.01.012  0.96
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  0.96
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  0.96
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  0.96
2015 Danysh HE, Mitchell LE, Zhang K, Scheurer ME, Lupo PJ. Traffic-related air pollution and the incidence of childhood central nervous system tumors: Texas, 2001-2009. Pediatric Blood & Cancer. 62: 1572-8. PMID 25962758 DOI: 10.1002/pbc.25549  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2014 Finnell RH, George TM, Mitchell LE. Neural Tube Defects Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.05586-0  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2010 Stanisławska-Sachadyn A, Woodside JV, Sayers CM, Yarnell JW, Young IS, Evans AE, Mitchell LE, Whitehead AS. The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B(12) status. European Journal of Clinical Nutrition. 64: 1338-43. PMID 20808328 DOI: 10.1038/ejcn.2010.157  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2009 StanisÅ‚awska-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  0.96
2009 Hammons AL, Summers CM, Woodside JV, McNulty H, Strain JJ, Young IS, Murray L, Boreham CA, Scott JM, Mitchell LE, Whitehead AS. Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1. Clinical Immunology (Orlando, Fla.). 133: 132-7. PMID 19625220 DOI: 10.1016/j.clim.2009.06.008  0.96
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  0.96
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  0.96
2009 Mitchell LE, Morales M, Khartulyari S, Huang Y, Murphy K, Mei M, Von Feldt JM, Blair IA, Whitehead AS. Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data. Clinical Biochemistry. 42: 1275-81. PMID 19427846 DOI: 10.1016/j.clinbiochem.2009.04.014  0.96
2009 Goldmuntz E, Driscoll DA, Emanuel BS, McDonald-McGinn D, Mei M, Zackai E, Mitchell LE. Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome Birth Defects Research Part a - Clinical and Molecular Teratology. 85: 125-129. PMID 18770859 DOI: 10.1002/bdra.20501  0.96
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  0.96
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  0.96
2008 Mitchell LE. Spina Bifida Research Resource: study design and participant characteristics. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 684-91. PMID 18553493 DOI: 10.1002/bdra.20465  0.96
2008 Summers CM, Hammons AL, Mitchell LE, Woodside JV, Yarnell JW, Young IS, Evans A, Whitehead AS. Influence of the cystathionine beta-synthase 844ins68 and methylenetetrahydrofolate reductase 677C>T polymorphisms on folate and homocysteine concentrations. European Journal of Human Genetics : Ejhg. 16: 1010-3. PMID 18398434 DOI: 10.1038/ejhg.2008.69  0.96
2008 StanisÅ‚awska-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  0.96
2008 StanisÅ‚awska-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  0.96
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  0.96
2006 Driscoll DA, Boland T, Emanuel BS, Kirschner RE, LaRossa D, Manson J, McDonald-McGinn D, Randall P, Solot C, Zackai E, Mitchell LE. Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome Cleft Palate-Craniofacial Journal. 43: 435-441. PMID 16854201 DOI: 10.1597/05-070R.1  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2005 Mansilla MA, Kimani J, Mitchell LE, Christensen K, Boomsma DI, Daack-Hirsch S, Nepomucena B, Wyszynski DF, Felix TM, Martin NG, Murray JC. Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 8: 39-46. PMID 15836809 DOI: 10.1375/1832427053435373  0.96
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  0.96
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  0.96
2005 Underkoffler LA, Mitchell LE, Abdulali ZS, Collins JN, Oakey RJ. Transmission ratio distortion in offspring of mouse heterozygous carriers of a (7.18) Robertsonian translocation. Genetics. 169: 843-8. PMID 15520265 DOI: 10.1534/genetics.104.032755  0.96
2004 Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. Spina bifida. Lancet (London, England). 364: 1885-95. PMID 15555669 DOI: 10.1016/S0140-6736(04)17445-X  0.96
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  0.96
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  0.96
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  0.96
2004 Brown KS, Kluijtmans LA, Young IS, Murray L, McMaster D, Woodside JV, Yarnell JW, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Mitchell LE, Whitehead AS. The 5,10-methylenetetrahydrofolate reductase C677T polymorphism interacts with smoking to increase homocysteine. Atherosclerosis. 174: 315-22. PMID 15136061 DOI: 10.1016/j.atherosclerosis.2004.01.023  0.96
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  0.96
2004 Brown KS, Kluijtmans LA, Young IS, McNulty H, Mitchell LE, Yarnell JW, Woodside JV, Boreham CA, McMaster D, Murray L, Strain JJ, Whitehead AS. The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects. Human Genetics. 114: 182-5. PMID 14586640 DOI: 10.1007/s00439-003-1039-9  0.96
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  0.96
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  0.96
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  0.96
2002 Underkoffler LA, Mitchell LE, Localio AR, Marchegiani SM, Morabito J, Collins JN, Oakey RJ. Molecular analysis of nondisjunction in mice heterozygous for a Robertsonian translocation. Genetics. 161: 1219-24. PMID 12136024  0.96
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  0.96
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  0.96
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  0.96
2000 Treloar SA, Macones GA, Mitchell LE, Martin NG. Genetic influences on premature parturition in an Australian twin sample. Twin Research : the Official Journal of the International Society For Twin Studies. 3: 80-2. PMID 10918619  0.96
1999 Digilio MC, Marino B, Giannotti A, Mingarelli R, Dallapicolla B, Goldmuntz E, Clark BJ, Mitchell LE, Cuneo BF, McDonald-Mcginn D, Zackair EH, Emanuel BS, Driscoll DA. Guidelines for 22q11 deletion screening of patients with conotruncal defects [1] (multiple letters) Journal of the American College of Cardiology. 33: 1746-1748. PMID 10334453 DOI: 10.1016/S0735-1097(99)00084-4  0.96
1999 Wyszynski DF, Mitchell LE. Report of the newly formed International Consortium for Oral Clefts Genetics. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 36: 174-8. PMID 10213064  0.96
1998 Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA. Frequency of 22q11 deletions in patients with conotruncal defects. Journal of the American College of Cardiology. 32: 492-8. PMID 9708481 DOI: 10.1016/S0735-1097(98)00259-9  0.96
1997 Driscoll DA, Emanuel BS, Mitchell LE, Budarf ML. PCR assay for screening patients at risk for 22q11.2 deletion Genetic Testing. 1: 109-113. PMID 10464634  0.96
1997 Mitchell LE. Genetic epidemiology of birth defects: Nonsyndromic cleft lip and neural tube defects Epidemiologic Reviews. 19: 61-68. PMID 9360903  0.96
1997 Mitchell LE, Christensen K. Evaluation of family history data for Danish twins with nonsyndromic cleft lip with or without cleft palate. American Journal of Medical Genetics. 72: 120-1. PMID 9295089 DOI: 10.1002/(SICI)1096-8628(19971003)72:1<120::AID-AJMG25>3.0.CO;2-S  0.96
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  0.96
1997 Mitchell LE. Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium. American Journal of Human Genetics. 60: 1006-7. PMID 9106551  0.96
1997 Mitchell LE, Duffy DL, Duffy P, Bellingham G, Martin NG. Genetic effects on variation in red-blood-cell folate in adults: implications for the familial aggregation of neural tube defects. American Journal of Human Genetics. 60: 433-8. PMID 9012417  0.96
1996 Mitchell LE, Christensen K. Analysis of the recurrence patterns for nonsyndromic cleft lip with or without cleft palate in the families of 3,073 Danish probands American Journal of Medical Genetics. 61: 371-376. PMID 8834050 DOI: 10.1002/(SICI)1096-8628(19960202)61:4<371::AID-AJMG12>3.0.CO;2-P  0.96
1996 Kane AA, Mitchell LE, Craven KP, Marsh JL. Observations on a recent increase in plagiocephaly without synostosis Pediatrics. 97: 877-885. PMID 8657530  0.96
1996 Christensen K, Mitchell LE. Familial recurrence-pattern analysis of nonsyndromic isolated cleft palate - A Danish registry study American Journal of Human Genetics. 58: 182-190. PMID 8554055  0.96
1995 Mitchell LE. Sequential analysis of marker data for a rare oligogenic disease Genetic Epidemiology. 12: 647-651. PMID 8787988 DOI: 10.1002/gepi.1370120621  0.96
1995 Mitchell LE, Healey SC, Chenevix-Trench G. Evidence for an Association between Nonsyndromic Cleft Lip with or Without Cleft Palate and a Gene Located on the Long Arm of Chromosome American Journal of Human Genetics. 57: 1130-1136. PMID 7485164  0.96
1994 Mitchell LE, Sprecher DL, Borecki IB, Rice T, Laskarzewski PM, Rao DC. Evidence for an association between dehydroepiandrosterone sulfate and nonfatal, premature myocardial infarction in males Circulation. 89: 89-93. PMID 8281699  0.96
1994 Mitchell LE, Nirmala A, Rice T, Chengal Reddy P, Rao DC. Commingling analysis of adiposity in an Indian population International Journal of Obesity. 18: 1-8. PMID 8130810  0.96
1994 Mitchell LE. Interpreting the evidence for an association between the retinoic acid receptor locus and non-syndromic cleft lip with or without cleft palate [5] Journal of Medical Genetics. 31: 425. PMID 7914931  0.96
1993 Rice T, Sprecher DL, Borecki IB, Mitchell LE, Laskarzewski PM, Rao DC. The cincinnati myocardial infarction and hormone family study: Family resemblance for dehydroepiandrosterone sulfate in control and myocardial infarction families Metabolism. 42: 1284-1290. PMID 8412740 DOI: 10.1016/0026-0495(93)90126-9  0.96
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  0.96
1993 Nirmala A, Mitchell LE, Rice T, Reddy PC, Rao DC. Assessment of adiposity in an Indian population: Familial correlations Genetic Epidemiology. 10: 133-143. PMID 8339927  0.96
1993 Rice T, Sprecher DL, Borecki IB, Mitchell LE, Laskarzewski PM, Rao DC. Cincinnati Myocardial Infarction and Hormone Family Study: Family resemblance for testosterone in random and MI families American Journal of Medical Genetics. 47: 542-549. PMID 8256821  0.96
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  0.96
1992 Mitchell LE, Risch N. Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: A reanalysis American Journal of Human Genetics. 51: 323-332. PMID 1642234  0.96
1990 Mitchell LE, Bracken MB. Reproductive versus chronologic age as a predictor of low birth weight, preterm delivery and intrauterine growth retardation in primiparous women Annals of Human Biology. 17: 377-386. PMID 2260840 DOI: 10.1080/03014469000001152  0.96
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