| Year |
Citation |
Score |
| 2023 |
Huang M, Lyu C, Liu N, Nembhard WN, Witte JS, Hobbs CA, Li M. A gene-based association test of interactions for maternal-fetal genotypes identifies genes associated with nonsyndromic congenital heart defects. Genetic Epidemiology. PMID 37341229 DOI: 10.1002/gepi.22533 |
0.339 |
|
| 2023 |
Webber DM, Li M, MacLeod SL, Tang X, Levy JW, Karim MA, Erickson SW, Hobbs CA. Gene-Folic Acid Interactions and Risk of Conotruncal Heart Defects: Results from the National Birth Defects Prevention Study. Genes. 14. PMID 36672920 DOI: 10.3390/genes14010180 |
0.322 |
|
| 2022 |
Owen MJ, Lefebvre S, Hansen C, Kunard CM, Dimmock DP, Smith LD, Scharer G, Mardach R, Willis MJ, Feigenbaum A, Niemi AK, Ding Y, Van Der Kraan L, Ellsworth K, Guidugli L, ... ... Hobbs CA, et al. An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases. Nature Communications. 13: 4057. PMID 35882841 DOI: 10.1038/s41467-022-31446-6 |
0.499 |
|
| 2022 |
Sanford Kobayashi E, Waldman B, Engorn BM, Perofsky K, Allred E, Briggs B, Gatcliffe C, Ramchandar N, Gold JJ, Doshi A, Ingulli EG, Thornburg CD, Benson W, Farnaes L, Chowdhury S, ... ... Hobbs C, et al. Cost Efficacy of Rapid Whole Genome Sequencing in the Pediatric Intensive Care Unit. Frontiers in Pediatrics. 9: 809536. PMID 35141181 DOI: 10.3389/fped.2021.809536 |
0.476 |
|
| 2022 |
Palmquist R, Jenkins SM, Bentley D, Miller C, Mao R, Meibos B, Bayrak-Toydemir P, Tvrdik T, Nadauld LD, Bleyl SB, Chowdhury S, Ostrander B, Flores-Daboub J, Longo N, Tristani-Firouzi M, ... Hobbs C, et al. Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics. Pediatric Research. PMID 35115709 DOI: 10.1038/s41390-022-01965-5 |
0.475 |
|
| 2021 |
Dimmock D, Caylor S, Waldman B, Benson W, Ashburner C, Carmichael JL, Carroll J, Cham E, Chowdhury S, Cleary J, D'Harlingue A, Doshi A, Ellsworth K, Galarreta CI, Hobbs C, et al. Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care. American Journal of Human Genetics. PMID 34089648 DOI: 10.1016/j.ajhg.2021.05.008 |
0.514 |
|
| 2021 |
Owen MJ, Niemi AK, Dimmock DP, Speziale M, Nespeca M, Chau KK, Van Der Kraan L, Wright MS, Hansen C, Veeraraghavan N, Ding Y, Lenberg J, Chowdhury S, Hobbs CA, Batalov S, et al. Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome. The New England Journal of Medicine. 384: 2159-2161. PMID 34077649 DOI: 10.1056/NEJMc2100365 |
0.447 |
|
| 2021 |
Sweeney NM, Nahas SA, Chowdhury S, Batalov S, Clark M, Caylor S, Cakici J, Nigro JJ, Ding Y, Veeraraghavan N, Hobbs C, Dimmock D, Kingsmore SF. Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 38. PMID 34039997 DOI: 10.1038/s41525-021-00205-9 |
0.546 |
|
| 2021 |
Sweeney NM, Nahas SA, Chowdhury S, Batalov S, Clark M, Caylor S, Cakici J, Nigro JJ, Ding Y, Veeraraghavan N, Hobbs C, Dimmock D, Kingsmore SF. Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 39. PMID 34039980 DOI: 10.1038/s41525-021-00206-8 |
0.547 |
|
| 2021 |
Sweeney NM, Nahas SA, Chowdhury S, Batalov S, Clark M, Caylor S, Cakici J, Nigro JJ, Ding Y, Veeraraghavan N, Hobbs C, Dimmock D, Kingsmore SF. Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. Npj Genomic Medicine. 6: 29. PMID 33888711 DOI: 10.1038/s41525-021-00192-x |
0.576 |
|
| 2020 |
Dimmock DP, Clark MM, Gaughran M, Cakici JA, Caylor SA, Clarke C, Feddock M, Chowdhury S, Salz L, Cheung C, Bird LM, Hobbs C, Wigby K, Farnaes L, Bloss CS, et al. An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm. American Journal of Human Genetics. 107: 942-952. PMID 33157007 DOI: 10.1016/j.ajhg.2020.10.003 |
0.538 |
|
| 2020 |
Richard MA, Sok P, Canon S, Nembhard WN, Brown AL, Peckham-Gregory EC, Ton M, Ehli EA, Kallsen NA, Peyton SA, Davies GE, Patel A, Zamilpa I, Hobbs CA, Scheurer ME, et al. Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias. Scientific Reports. 10: 12715. PMID 32728162 DOI: 10.1038/S41598-020-69725-1 |
0.31 |
|
| 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 |
0.414 |
|
| 2020 |
Ramchandar N, Ding Y, Farnaes L, Dimmock D, Hobbs C, Kingsmore SF, Bainbridge M. Diagnosis of cytomegalovirus infection from clinical whole genome sequencing. Scientific Reports. 10: 11020. PMID 32620939 DOI: 10.1038/S41598-020-67656-5 |
0.306 |
|
| 2020 |
Kingsmore SF, Ramchandar N, James K, Niemi AK, Feigenbaum A, Ding Y, Benson W, Hobbs C, Nahas S, Chowdhury S, Dimmock D. Mortality in a neonate with molybdenum cofactor deficiency illustrates the need for a comprehensive rapid precision medicine system. Cold Spring Harbor Molecular Case Studies. 6. PMID 32014857 DOI: 10.1101/mcs.a004705 |
0.488 |
|
| 2019 |
Lyu C, Webber DM, MacLeod SL, Hobbs CA, Li M. Gene-by-gene interactions associated with the risk of conotruncal heart defects. Molecular Genetics & Genomic Medicine. e1010. PMID 31851787 DOI: 10.1002/Mgg3.1010 |
0.372 |
|
| 2019 |
Kingsmore SF, Cakici JA, Clark MM, Gaughran M, Feddock M, Batalov S, Bainbridge MN, Carroll J, Caylor SA, Clarke C, Ding Y, Ellsworth K, Farnaes L, Hildreth A, Hobbs C, et al. A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants. American Journal of Human Genetics. PMID 31564432 DOI: 10.1016/J.Ajhg.2019.08.009 |
0.588 |
|
| 2019 |
Yu X, Nassar N, Mastroiacovo P, Canfield M, Groisman B, Bermejo-Sánchez E, Ritvanen A, Kiuru-Kuhlefelt S, Benavides A, Sipek A, Pierini A, Bianchi F, Källén K, Gatt M, Morgan M, ... ... Hobbs CA, et al. Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980-2010. European Urology. PMID 31300237 DOI: 10.1016/J.Eururo.2019.06.027 |
0.363 |
|
| 2019 |
Richard MA, Sok P, Canon S, Brown AL, Peckham-Gregory EC, Nembhard WN, Carmichael SL, Ehli EA, Kallsen NA, Peyton SA, Davies GE, Patel A, Zamilpa I, Wyatt RA, Hobbs CA, et al. The role of genetic variation in DGKK on moderate and severe hypospadias. Birth Defects Research. PMID 31102501 DOI: 10.1002/Bdr2.1522 |
0.357 |
|
| 2018 |
Tang X, Eberhart JK, Cleves MA, Li J, Li M, MacLeod S, Nembhard WN, Hobbs CA. PDGFRA gene, maternal binge drinking and obstructive heart defects. Scientific Reports. 8: 11083. PMID 30038270 DOI: 10.1038/S41598-018-29160-9 |
0.405 |
|
| 2018 |
Nembhard WN, Tang X, Li J, MacLeod SL, Levy J, Schaefer GB, Hobbs CA. A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects. American Journal of Medical Genetics. Part A. PMID 29399948 DOI: 10.1002/Ajmg.A.38611 |
0.403 |
|
| 2016 |
Ailes EC, Gilboa SM, Gill SK, Broussard CS, Crider KS, Berry RJ, Carter TC, Hobbs CA, Interrante JD, Reefhuis J. Association between antibiotic use among pregnant women with urinary tract infections in the first trimester and birth defects, National Birth Defects Prevention Study 1997 to 2011. Birth Defects Research. Part a, Clinical and Molecular Teratology. 106: 940-949. PMID 27891788 DOI: 10.1002/Bdra.23570 |
0.35 |
|
| 2016 |
Dawson AL, Tinker SC, Jamieson DJ, Hobbs CA, Berry RJ, Rasmussen SA, Anderka M, Keppler-Noreuil KM, Lin AE, Reefhuis J. Twinning and major birth defects, National Birth Defects Prevention Study, 1997-2007. Journal of Epidemiology and Community Health. PMID 27325867 DOI: 10.1136/Jech-2015-206302 |
0.431 |
|
| 2016 |
Li M, Li J, He Z, Lu Q, Witte JS, Macleod SL, Hobbs CA, Cleves MA. Testing Allele Transmission of an SNP Set Using a Family-Based Generalized Genetic Random Field Method. Genetic Epidemiology. PMID 27061818 DOI: 10.1002/Gepi.21970 |
0.328 |
|
| 2015 |
Li M, Li J, Wei C, Lu Q, Tang X, Erickson SW, MacLeod SL, Hobbs CA. A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects. Annals of Human Genetics. PMID 26612412 DOI: 10.1111/Ahg.12139 |
0.421 |
|
| 2015 |
Simeone RM, Oster ME, Hobbs CA, Robbins JM, Thomas Collins R, Honein MA. Factors associated with inpatient hospitalizations among patients aged 1 to 64 years with congenital heart defects, Arkansas 2006 to 2011. Birth Defects Research. Part a, Clinical and Molecular Teratology. 103: 589-96. PMID 26172576 DOI: 10.1002/Bdra.23402 |
0.312 |
|
| 2015 |
Simeone RM, Oster ME, Hobbs CA, Robbins JM, Collins RT, Honein MA. Population-based study of hospital costs for hospitalizations of infants, children, and adults with a congenital heart defect, Arkansas 2006 to 2011. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26069215 DOI: 10.1002/Bdra.23379 |
0.304 |
|
| 2015 |
Webber DM, MacLeod SL, Bamshad MJ, Shaw GM, Finnell RH, Shete SS, Witte JS, Erickson SW, Murphy LD, Hobbs C. Developments in our understanding of the genetic basis of birth defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26033863 DOI: 10.1002/Bdra.23385 |
0.432 |
|
| 2015 |
Reefhuis J, Gilboa SM, Anderka M, Browne ML, Feldkamp ML, Hobbs CA, Jenkins MM, Langlois PH, Newsome KB, Olshan AF, Romitti PA, Shapira SK, Shaw GM, Tinker SC, Honein MA, et al. The national birth defects prevention study: A review of the methods. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26033852 DOI: 10.1002/Bdra.23384 |
0.416 |
|
| 2015 |
Tang X, Hobbs CA, Cleves MA, Erickson SW, MacLeod SL, Malik S. Genetic variation affects congenital heart defect susceptibility in offspring exposed to maternal tobacco use. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26033827 DOI: 10.1002/Bdra.23370 |
0.445 |
|
| 2015 |
Tang X, Cleves MA, Nick TG, Li M, MacLeod SL, Erickson SW, Li J, Shaw GM, Mosley BS, Hobbs CA. Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation. American Journal of Medical Genetics. Part A. 167: 1231-42. PMID 25846410 DOI: 10.1002/Ajmg.A.36867 |
0.432 |
|
| 2015 |
Dawson AL, Tinker SC, Jamieson DJ, Hobbs CA, Rasmussen SA, Reefhuis J. Epidemiology of twinning in the National Birth Defects Prevention Study, 1997 to 2007. Birth Defects Research. Part a, Clinical and Molecular Teratology. 103: 85-99. PMID 25359509 DOI: 10.1002/Bdra.23325 |
0.432 |
|
| 2015 |
Miquel-Verges F, Mosley BS, Block AS, Hobbs CA. A spectrum project: preterm birth and small-for-gestational age among infants with birth defects. Journal of Perinatology : Official Journal of the California Perinatal Association. 35: 198-203. PMID 25275696 DOI: 10.1038/Jp.2014.180 |
0.406 |
|
| 2014 |
Tang X, Nick TG, Cleves MA, Erickson SW, Li M, Li J, MacLeod SL, Hobbs CA. Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects. Plos One. 9: e108903. PMID 25275547 DOI: 10.1371/Journal.Pone.0108903 |
0.417 |
|
| 2014 |
Li M, Cleves MA, Mallick H, Erickson SW, Tang X, Nick TG, Macleod SL, Hobbs CA. A genetic association study detects haplotypes associated with obstructive heart defects. Human Genetics. 133: 1127-38. PMID 24894164 DOI: 10.1007/S00439-014-1453-1 |
0.429 |
|
| 2014 |
Li M, Erickson SW, Hobbs CA, Li J, Tang X, Nick TG, Macleod SL, Cleves MA. Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression. Genetic Epidemiology. 38: 198-208. PMID 24585533 DOI: 10.1002/Gepi.21793 |
0.433 |
|
| 2014 |
Hobbs CA, Cleves MA, Macleod SL, Erickson SW, Tang X, Li J, Li M, Nick T, Malik S. Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 116-26. PMID 24535845 DOI: 10.1002/Bdra.23225 |
0.403 |
|
| 2014 |
Shaw GM, Yang W, Carmichael SL, Vollset SE, Hobbs CA, Lammer EJ, Ueland PM. One-carbon metabolite levels in mid-pregnancy and risks of conotruncal heart defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 107-15. PMID 24532477 DOI: 10.1002/Bdra.23224 |
0.381 |
|
| 2014 |
Hobbs CA, Chowdhury S, Cleves MA, Erickson S, MacLeod SL, Shaw GM, Shete S, Witte JS, Tycko B. Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics. Jama Pediatrics. 168: 371-7. PMID 24515445 DOI: 10.1001/Jamapediatrics.2013.4858 |
0.629 |
|
| 2014 |
Ailes EC, Gilboa SM, Riehle-Colarusso T, Johnson CY, Hobbs CA, Correa A, Honein MA. Prenatal diagnosis of nonsyndromic congenital heart defects. Prenatal Diagnosis. 34: 214-22. PMID 24222433 DOI: 10.1002/Pd.4282 |
0.435 |
|
| 2014 |
Weedn AE, Mosley BS, Cleves MA, Waller DK, Canfield MA, Correa A, Hobbs CA. Maternal reporting of prenatal ultrasounds among women in the National Birth Defects Prevention Study. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 4-12. PMID 24123727 DOI: 10.1097/Ogx.0000000000000060 |
0.437 |
|
| 2014 |
Glidewell J, Reefhuis J, Rasmussen SA, Woomert A, Hobbs C, Romitti PA, Crider KS. Factors affecting maternal participation in the genetic component of the National Birth Defects Prevention Study-United States, 1997-2007. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 329-37. PMID 24071796 DOI: 10.1038/Gim.2013.143 |
0.419 |
|
| 2013 |
Sotres-Alvarez D, Siega-Riz AM, Herring AH, Carmichael SL, Feldkamp ML, Hobbs CA, Olshan AF. Maternal dietary patterns are associated with risk of neural tube and congenital heart defects. American Journal of Epidemiology. 177: 1279-88. PMID 23639938 DOI: 10.1093/Aje/Kws349 |
0.361 |
|
| 2013 |
Hunter JE, Allen EG, Shin M, Bean LJ, Correa A, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL. The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 698-705. PMID 23558253 DOI: 10.1038/Gim.2013.34 |
0.365 |
|
| 2013 |
Blossom SJ, Rau JL, Best TH, Bornemeier RA, Hobbs CA. Increased maternal cytokine production and congenital heart defects. Journal of Reproductive Immunology. 97: 204-10. PMID 23428339 DOI: 10.1016/J.Jri.2012.12.004 |
0.376 |
|
| 2013 |
Hollis ND, Allen EG, Oliver TR, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL, Bean LJ. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project. American Journal of Medical Genetics. Part A. 161: 438-44. PMID 23401135 DOI: 10.1002/Ajmg.A.35796 |
0.424 |
|
| 2012 |
Canon S, Mosley B, Chipollini J, Purifoy JA, Hobbs C. Epidemiological Assessment of Hypospadias by Degree of Severity The Journal of Urology. 188: 2362-2366. PMID 23088968 DOI: 10.1016/J.Juro.2012.08.007 |
0.427 |
|
| 2012 |
Chowdhury S, Hobbs CA, MacLeod SL, Cleves MA, Melnyk S, James SJ, Hu P, Erickson SW. Associations between maternal genotypes and metabolites implicated in congenital heart defects. Molecular Genetics and Metabolism. 107: 596-604. PMID 23059056 DOI: 10.1016/J.Ymgme.2012.09.022 |
0.592 |
|
| 2012 |
Chandler AL, Hobbs CA, Mosley BS, Berry RJ, Canfield MA, Qi YP, Siega-Riz AM, Shaw GM. Neural tube defects and maternal intake of micronutrients related to one-carbon metabolism or antioxidant activity. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 864-74. PMID 22933447 DOI: 10.1002/Bdra.23068 |
0.346 |
|
| 2012 |
Correa A, Gilboa SM, Botto LD, Moore CA, Hobbs CA, Cleves MA, Riehle-Colarusso TJ, Waller DK, Reece EA. Lack of periconceptional vitamins or supplements that contain folic acid and diabetes mellitus-associated birth defects. American Journal of Obstetrics and Gynecology. 206: 218.e1-13. PMID 22284962 DOI: 10.1016/J.Ajog.2011.12.018 |
0.307 |
|
| 2011 |
Bean LJ, Allen EG, Tinker SW, Hollis ND, Locke AE, Druschel C, Hobbs CA, O'Leary L, Romitti PA, Royle MH, Torfs CP, Dooley KJ, Freeman SB, Sherman SL. Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 885-93. PMID 21987466 DOI: 10.1002/Bdra.22848 |
0.47 |
|
| 2011 |
Olshan AF, Hobbs CA, Shaw GM. Discovery of genetic susceptibility factors for human birth defects: an opportunity for a National Agenda. American Journal of Medical Genetics. Part A. 155: 1794-7. PMID 21739590 DOI: 10.1002/Ajmg.A.34103 |
0.373 |
|
| 2011 |
Hobbs CA, MacLeod SL, Jill James S, Cleves MA. Congenital heart defects and maternal genetic, metabolic, and lifestyle factors. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 195-203. PMID 21384532 DOI: 10.1002/Bdra.20784 |
0.367 |
|
| 2011 |
Chowdhury S, Erickson SW, MacLeod SL, Cleves MA, Hu P, Karim MA, Hobbs CA. Maternal genome-wide DNA methylation patterns and congenital heart defects. Plos One. 6: e16506. PMID 21297937 DOI: 10.1371/Journal.Pone.0016506 |
0.589 |
|
| 2011 |
Cleves MA, Hobbs CA, Zhao W, Krakowiak PA, MacLeod SL. Association between selected folate pathway polymorphisms and nonsyndromic limb reduction defects: a case-parental analysis. Paediatric and Perinatal Epidemiology. 25: 124-34. PMID 21281325 DOI: 10.1111/J.1365-3016.2010.01160.X |
0.412 |
|
| 2011 |
Chowdhury S, Cleves MA, MacLeod SL, James SJ, Zhao W, Hobbs CA. Maternal DNA hypomethylation and congenital heart defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 69-76. PMID 21254366 DOI: 10.1002/Bdra.20761 |
0.57 |
|
| 2010 |
Robbins JM, Damiano P, Druschel CM, Hobbs CA, Romitti PA, Austin AA, Tyler M, Reading JA, Burnett W. Prenatal diagnosis of orofacial clefts: association with maternal satisfaction, team care, and treatment outcomes. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 47: 476-81. PMID 20822456 DOI: 10.1597/08-177 |
0.428 |
|
| 2010 |
Hobbs CA, Cleves MA, Karim MA, Zhao W, MacLeod SL. Maternal folate-related gene environment interactions and congenital heart defects. Obstetrics and Gynecology. 116: 316-22. PMID 20664391 DOI: 10.1097/Aog.0B013E3181E80979 |
0.384 |
|
| 2009 |
Crider KS, Cleves MA, Reefhuis J, Berry RJ, Hobbs CA, Hu DJ. Antibacterial medication use during pregnancy and risk of birth defects: National Birth Defects Prevention Study. Archives of Pediatrics & Adolescent Medicine. 163: 978-85. PMID 19884587 DOI: 10.1001/Archpediatrics.2009.188 |
0.402 |
|
| 2009 |
Mac Bird T, Robbins JM, Druschel C, Cleves MA, Yang S, Hobbs CA. Demographic and environmental risk factors for gastroschisis and omphalocele in the National Birth Defects Prevention Study. Journal of Pediatric Surgery. 44: 1546-51. PMID 19635303 DOI: 10.1016/J.Jpedsurg.2008.10.109 |
0.325 |
|
| 2009 |
Johnson CY, Honein MA, Hobbs CA, Rasmussen SA. Prenatal diagnosis of orofacial clefts, National Birth Defects Prevention Study, 1998-2004. Prenatal Diagnosis. 29: 833-9. PMID 19455588 DOI: 10.1002/Pd.2293 |
0.457 |
|
| 2009 |
Burke BL, Robbins JM, Bird TM, Hobbs CA, Nesmith C, Tilford JM. Trends in hospitalizations for neonatal jaundice and kernicterus in the United States, 1988-2005 Pediatrics. 123: 524-532. PMID 19171618 DOI: 10.1542/Peds.2007-2915 |
0.335 |
|
| 2009 |
Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL. Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects. Human Genetics. 125: 41-52. PMID 19050929 DOI: 10.1007/S00439-008-0603-8 |
0.393 |
|
| 2009 |
Freeman SB, Torfs CP, Romitti PA, Royle MH, Druschel C, Hobbs CA, Sherman SL. Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects. Clinical Genetics. 75: 180-4. PMID 19021635 DOI: 10.1111/J.1399-0004.2008.01110.X |
0.454 |
|
| 2009 |
Reefhuis J, Honein MA, Schieve LA, Correa A, Hobbs CA, Rasmussen SA. Assisted reproductive technology and major structural birth defects in the United States. Human Reproduction (Oxford, England). 24: 360-6. PMID 19010807 DOI: 10.1093/Humrep/Den387 |
0.453 |
|
| 2009 |
Mosley BS, Cleves MA, Siega-Riz AM, Shaw GM, Canfield MA, Waller DK, Werler MM, Hobbs CA. Neural tube defects and maternal folate intake among pregnancies conceived after folic acid fortification in the United States. American Journal of Epidemiology. 169: 9-17. PMID 18953063 DOI: 10.1093/Aje/Kwn331 |
0.39 |
|
| 2009 |
Reefhuis J, Honein MA, Schieve LA, Correa A, Hobbs CA, Rasmussen SA. Reply: ART and major structural birth defects in the USA Human Reproduction. 24: 1766. DOI: 10.1093/Humrep/Dep097 |
0.376 |
|
| 2008 |
Waller DK, Correa A, Vo TM, Wang Y, Hobbs C, Langlois PH, Pearson K, Romitti PA, Shaw GM, Hecht JT. The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the US. American Journal of Medical Genetics. Part A. 146: 2385-9. PMID 18698630 DOI: 10.1002/Ajmg.A.32485 |
0.322 |
|
| 2008 |
Correa A, Gilboa SM, Besser LM, Botto LD, Moore CA, Hobbs CA, Cleves MA, Riehle-Colarusso TJ, Waller DK, Reece EA. Diabetes mellitus and birth defects. American Journal of Obstetrics and Gynecology. 199: 237.e1-9. PMID 18674752 DOI: 10.1016/j.ajog.2008.06.028 |
0.305 |
|
| 2008 |
Cleves MA, Malik S, Yang S, Carter TC, Hobbs CA. Maternal urinary tract infections and selected cardiovascular malformations. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 464-73. PMID 18452156 DOI: 10.1002/Bdra.20460 |
0.311 |
|
| 2008 |
Malik S, Cleves MA, Honein MA, Romitti PA, Botto LD, Yang S, Hobbs CA. Maternal smoking and congenital heart defects. Pediatrics. 121: e810-6. PMID 18381510 DOI: 10.1542/Peds.2007-1519 |
0.37 |
|
| 2008 |
Freeman SB, Bean LH, Allen EG, Tinker SW, Locke AE, Druschel C, Hobbs CA, Romitti PA, Royle MH, Torfs CP, Dooley KJ, Sherman SL. Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 173-80. PMID 18344706 DOI: 10.1097/Gim.0B013E3181634867 |
0.425 |
|
| 2008 |
Luben TJ, Nuckols JR, Mosley BS, Hobbs C, Reif JS. Maternal exposure to water disinfection by-products during gestation and risk of hypospadias. Occupational and Environmental Medicine. 65: 420-9. PMID 18032532 DOI: 10.1136/Oem.2007.034256 |
0.339 |
|
| 2007 |
Cleves MA, Hobbs CA, Cleves PA, Tilford JM, Bird TM, Robbins JM. Congenital defects among liveborn infants with Down syndrome. Birth Defects Research. Part a, Clinical and Molecular Teratology. 79: 657-63. PMID 17696161 DOI: 10.1002/Bdra.20393 |
0.446 |
|
| 2007 |
Waller DK, Shaw GM, Rasmussen SA, Hobbs CA, Canfield MA, Siega-Riz AM, Gallaway MS, Correa A. Prepregnancy obesity as a risk factor for structural birth defects. Archives of Pediatrics & Adolescent Medicine. 161: 745-50. PMID 17679655 DOI: 10.1001/Archpedi.161.8.745 |
0.394 |
|
| 2007 |
Malik S, Cleves MA, Zhao W, Correa A, Hobbs CA. Association between congenital heart defects and small for gestational age. Pediatrics. 119: e976-82. PMID 17387169 DOI: 10.1542/Peds.2006-2742 |
0.445 |
|
| 2007 |
Freeman SB, Allen EG, Oxford-Wright CL, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL. The National Down Syndrome Project: design and implementation. Public Health Reports (Washington, D.C. : 1974). 122: 62-72. PMID 17236610 DOI: 10.1177/003335490712200109 |
0.417 |
|
| 2006 |
Robbins JM, Bird TM, Tilford JM, Reading JA, Cleves MA, Aitken ME, Druschel CM, Hobbs CA. Reduction in newborns with discharge coding of in utero alcohol effects in the United States, 1993 to 2002. Archives of Pediatrics & Adolescent Medicine. 160: 1224-31. PMID 17146019 DOI: 10.1001/Archpedi.160.12.1224 |
0.311 |
|
| 2006 |
Bird TM, Hobbs CA, Cleves MA, Tilford JM, Robbins JM. National rates of birth defects among hospitalized newborns. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 762-9. PMID 17063529 DOI: 10.1002/Bdra.20323 |
0.403 |
|
| 2006 |
Canfield MA, Honein MA, Yuskiv N, Xing J, Mai CT, Collins JS, Devine O, Petrini J, Ramadhani TA, Hobbs CA, Kirby RS. National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999-2001. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 747-56. PMID 17051527 DOI: 10.1002/Bdra.20294 |
0.403 |
|
| 2006 |
Robbins JM, Tilford JM, Bird TM, Cleves MA, Reading JA, Hobbs CA. Hospitalizations of newborns with folate-sensitive birth defects before and after fortification of foods with folic acid. Pediatrics. 118: 906-15. PMID 16950980 DOI: 10.1542/Peds.2005-2784 |
0.388 |
|
| 2006 |
Zhao W, Mosley BS, Cleves MA, Melnyk S, James SJ, Hobbs CA. Neural tube defects and maternal biomarkers of folate, homocysteine, and glutathione metabolism. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 230-6. PMID 16575882 DOI: 10.1002/Bdra.20240 |
0.346 |
|
| 2006 |
Hobbs CA, Malik S, Zhao W, James SJ, Melnyk S, Cleves MA. Maternal homocysteine and congenital heart defects. Journal of the American College of Cardiology. 47: 683-5. PMID 16458157 DOI: 10.1016/J.Jacc.2005.11.013 |
0.42 |
|
| 2006 |
Hobbs CA, James SJ, Jernigan S, Melnyk S, Lu Y, Malik S, Cleves MA. Congenital heart defects, maternal homocysteine, smoking, and the 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene: evaluating gene-environment interactions. American Journal of Obstetrics and Gynecology. 194: 218-24. PMID 16389035 DOI: 10.1016/J.Ajog.2005.06.016 |
0.366 |
|
| 2006 |
Hobbs CA, James SJ, Parsian A, Krakowiak PA, Jernigan S, Greenhaw JJ, Lu Y, Cleves MA. Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene. Journal of Medical Genetics. 43: 162-6. PMID 15951337 DOI: 10.1136/Jmg.2005.032656 |
0.398 |
|
| 2005 |
Hobbs CA, Cleves MA, Zhao W, Melnyk S, James SJ. Congenital heart defects and maternal biomarkers of oxidative stress. The American Journal of Clinical Nutrition. 82: 598-604. PMID 16155273 DOI: 10.1093/Ajcn.82.3.598 |
0.36 |
|
| 2005 |
Hobbs CA, Cleves MA, Melnyk S, Zhao W, James SJ. Congenital heart defects and abnormal maternal biomarkers of methionine and homocysteine metabolism. The American Journal of Clinical Nutrition. 81: 147-53. PMID 15640474 DOI: 10.1093/Ajcn/81.1.147 |
0.409 |
|
| 2005 |
Hobbs CA, Cleves MA, Keith C, Ghaffar S, James SJ. NKX2.5 and congenital heart defects: A population-based study. American Journal of Medical Genetics. Part A. 134: 223-5. PMID 15633194 DOI: 10.1002/Ajmg.A.30509 |
0.335 |
|
| 2005 |
Bird TM, Tilford JM, Cleves MA, Hobbs CA, Robbins JM. 176 Surveying Birth Defects In States With Limited Surveillance Systems: The Value Of Administrative Data Journal of Investigative Medicine. 53. DOI: 10.2310/6650.2005.00006.175 |
0.363 |
|
| 2004 |
Simmons CJ, Mosley BS, Fulton-Bond CA, Hobbs CA. Birth defects in Arkansas: is folic acid fortification making a difference? Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 559-64. PMID 15368553 DOI: 10.1002/Bdra.20063 |
0.401 |
|
| 2004 |
Cleves MA, Hobbs CA. Collaborative strategies for unraveling the complexity of birth defects. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 15: 35-8. PMID 15101609 DOI: 10.1080/14767050310001650699 |
0.384 |
|
| 2004 |
Cleves MA, Hobbs CA, Collins HB, Andrews N, Smith LN, Robbins JM. Folic acid use by women receiving routine gynecologic care. Obstetrics and Gynecology. 103: 746-53. PMID 15051568 DOI: 10.1097/01.Aog.0000117084.02395.A0 |
0.301 |
|
| 2004 |
Cleves MA, Savell VH, Raj S, Zhao W, Correa A, Werler MM, Hobbs CA. Maternal use of acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs), and muscular ventricular septal defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 107-13. PMID 15039924 DOI: 10.1002/Bdra.20005 |
0.468 |
|
| 2003 |
Cleves MA, Ghaffar S, Zhao W, Mosley BS, Hobbs CA. First-year survival of infants born with congenital heart defects in Arkansas (1993-1998): a survival analysis using registry data. Birth Defects Research. Part a, Clinical and Molecular Teratology. 67: 662-8. PMID 14703791 DOI: 10.1002/Bdra.10119 |
0.402 |
|
| 2003 |
Araneta MR, Schlangen KM, Edmonds LD, Destiche DA, Merz RD, Hobbs CA, Flood TJ, Harris JA, Krishnamurti D, Gray GC. Prevalence of birth defects among infants of Gulf War veterans in Arkansas, Arizona, California, Georgia, Hawaii, and Iowa, 1989-1993. Birth Defects Research. Part a, Clinical and Molecular Teratology. 67: 246-60. PMID 12854660 DOI: 10.1002/Bdra.10033 |
0.437 |
|
| 2003 |
Williams LJ, Mai CT, Edmonds LD, Shaw GM, Kirby RS, Hobbs CA, Sever LE, Miller LA, Meaney FJ, Levitt M. Prevalence of Spina Bifida and Anencephaly During the Transition to Mandatory Folic Acid Fortification in the United States Obstetrical & Gynecological Survey. 58: 90-92. DOI: 10.1097/00006254-200302000-00004 |
0.3 |
|
| 2002 |
Hobbs CA, Cleves MA, Lauer RM, Burns TL, James SJ. Preferential transmission of the MTHFR 677 T allele to infants with Down syndrome: implications for a survival advantage. American Journal of Medical Genetics. 113: 9-14. PMID 12400059 DOI: 10.1002/Ajmg.10704 |
0.343 |
|
| 2002 |
Mosley BS, Simmons CJ, Cleves MA, Hobbs CA. Regional bias in birth defect prevalence rates for Arkansas: influence of incomplete ascertainment along surveillance system borders. Teratology. 66: S36-40. PMID 12239743 DOI: 10.1002/Tera.90009 |
0.358 |
|
| 2002 |
Hobbs CA, Cleves MA, Simmons CJ. Genetic epidemiology and congenital malformations: from the chromosome to the crib. Archives of Pediatrics & Adolescent Medicine. 156: 315-20. PMID 11929362 DOI: 10.1001/Archpedi.156.4.315 |
0.457 |
|
| 2001 |
Yoon PW, Rasmussen SA, Lynberg MC, Moore CA, Anderka M, Carmichael SL, Costa P, Druschel C, Hobbs CA, Romitti PA, Langlois PH, Edmonds LD. The National Birth Defects Prevention Study. Public Health Reports (Washington, D.C. : 1974). 116: 32-40. PMID 11889273 DOI: 10.1093/Phr/116.S1.32 |
0.473 |
|
| 2001 |
Tilford JM, Robbins JM, Hobbs CA. Improving estimates of caregiver time cost and family impact associated with birth defects. Teratology. 64: S37-41. PMID 11745843 DOI: 10.1002/Tera.1097 |
0.303 |
|
| 2001 |
Hobbs CA, Hopkins SE, Simmons CJ. Sources of variability in birth defects prevalence rates. Teratology. 64: S8-S13. PMID 11745838 DOI: 10.1002/Tera.1078 |
0.384 |
|
| 2000 |
Hobbs CA, Sherman SL, Yi P, Hopkins SE, Torfs CP, Hine RJ, Pogribna M, Rozen R, James SJ. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome. American Journal of Human Genetics. 67: 623-30. PMID 10930360 DOI: 10.1086/303055 |
0.362 |
|
| 1997 |
Hobbs CA, Casey PH, Kirby RS. The Association of Birth Defects and Failure to Thrive. † 444 Pediatric Research. 41: 76-76. DOI: 10.1203/00006450-199704001-00464 |
0.394 |
|
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