Andrew T. DeWan - Publications

Affiliations: 
Chronic Disease Epidemiology Yale University, New Haven, CT 
Area:
Epidemiology, Genetics

39 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
2016 Spracklen CN, Smith CJ, Saftlas AF, Triche EW, Bjonnes A, Keating BJ, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia. Hypertension in Pregnancy. 1-10. PMID 27657194 DOI: 10.1080/10641955.2016.1223303  0.44
2016 Murk W, DeWan AT. Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma. Bmc Genetics. 17: 102. PMID 27387956 DOI: 10.1186/s12863-016-0376-3  0.44
2016 Wang L, Salinas YD, DeWan AT. Gene-based analysis identified the gene ZNF248 is associated with late-onset asthma in African Americans. Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology. PMID 27238579 DOI: 10.1016/j.anai.2016.05.005  0.44
2016 Askim Å, Mehl A, Paulsen J, DeWan AT, Vestrheim DF, Åsvold BO, Damås JK, Solligård E. Epidemiology and outcome of sepsis in adult patients with Streptococcus pneumoniae infection in a Norwegian county 1993-2011: an observational study. Bmc Infectious Diseases. 16: 223. PMID 27216810 DOI: 10.1186/s12879-016-1553-8  0.44
2016 Jacobs DI, Qin Q, Lerro MC, Fu AN, Dubrow R, Claus EB, DeWan AT, Wang G, Lin H, Zhu Y. PIWI-interacting RNAs in Gliomagenesis: Evidence from Post-GWAS and Functional Analyses. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 27197292 DOI: 10.1158/1055-9965.EPI-16-0047  0.44
2016 Uzun A, Triche EW, Schuster J, Dewan AT, Padbury JF. dbPEC: a comprehensive literature-based database for preeclampsia related genes and phenotypes. Database : the Journal of Biological Databases and Curation. 2016. PMID 26946289 DOI: 10.1093/database/baw006  0.44
2015 Wang L, Murk W, DeWan AT. Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. Plos One. 10: e0144114. PMID 26672748 DOI: 10.1371/journal.pone.0144114  0.44
2015 Smith CJ, Saftlas AF, Spracklen CN, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. American Journal of Hypertension. PMID 26002928 DOI: 10.1093/ajh/hpv069  0.44
2015 Murk W, Bracken MB, DeWan AT. Confronting the missing epistasis problem: on the reproducibility of gene-gene interactions. Human Genetics. 134: 837-49. PMID 25998948 DOI: 10.1007/s00439-015-1564-3  0.44
2015 Spracklen CN, Saftlas AF, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia. American Journal of Hypertension. 28: 915-23. PMID 25523295 DOI: 10.1093/ajh/hpu242  0.44
2015 Egan KB, Ettinger AS, DeWan AT, Holford TR, Holmen TL, Bracken MB. Longitudinal associations between asthma and general and abdominal weight status among Norwegian adolescents and young adults: the HUNT Study. Pediatric Obesity. 10: 345-52. PMID 25405952 DOI: 10.1111/ijpo.271  0.44
2014 Patterson VL, Zullo AJ, Koenig C, Stoessel S, Jo H, Liu X, Han J, Choi M, DeWan AT, Thomas JL, Kuan CY, Hoh J. Neural-specific deletion of Htra2 causes cerebellar neurodegeneration and defective processing of mitochondrial OPA1. Plos One. 9: e115789. PMID 25531304 DOI: 10.1371/journal.pone.0115789  0.44
2014 Egan KB, Ettinger AS, DeWan AT, Holford TR, Holmen TL, Bracken MB. General, but not abdominal, overweight increases odds of asthma among Norwegian adolescents: the Young-HUNT study. Acta Paediatrica (Oslo, Norway : 1992). 103: 1270-6. PMID 25131148 DOI: 10.1111/apa.12775  0.44
2014 Triche EW, Uzun A, DeWan AT, Kurihara I, Liu J, Occhiogrosso R, Shen B, Parker J, Padbury JF. Bioinformatic approach to the genetics of preeclampsia. Obstetrics and Gynecology. 123: 1155-61. PMID 24807322 DOI: 10.1097/AOG.0000000000000293  0.44
2014 Hoang D, Broer N, Roman SA, Yao X, Abitbol N, Li F, Sosa JA, Sue GR, DeWan AT, Wong ML, Licinio J, Simpson C, Li AY, Pizzoferrato N, Narayan D. Leptin signaling and hyperparathyroidism: clinical and genetic associations. Journal of the American College of Surgeons. 218: 1239-1250.e4. PMID 24468228 DOI: 10.1016/j.jamcollsurg.2013.11.013  0.44
2013 Zhao L, Bracken MB, DeWan AT. Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. Annals of Human Genetics. 77: 277-87. PMID 23551011 DOI: 10.1111/ahg.12021  0.44
2013 Uzun A, Dewan AT, Istrail S, Padbury JF. Pathway-based genetic analysis of preterm birth. Genomics. 101: 163-70. PMID 23298525 DOI: 10.1016/j.ygeno.2012.12.005  0.44
2013 Zhao L, Bracken MB, Dewan AT, Chen S. Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) and pre-eclampsia: a systematic review and meta-analysis. Molecular Human Reproduction. 19: 136-43. PMID 23180602 DOI: 10.1093/molehr/gas056  0.44
2012 Jacobs DI, Walsh KM, Wrensch M, Wiencke J, Jenkins R, Houlston RS, Bondy M, Simon M, Sanson M, Gousias K, Schramm J, Labussière M, Di Stefano AL, Wichmann HE, Müller-Nurasyid M, ... ... Dewan AT, et al. Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach. Frontiers in Genetics. 3: 203. PMID 23091480 DOI: 10.3389/fgene.2012.00203  0.44
2012 Popova EY, Xu X, DeWan AT, Salzberg AC, Berg A, Hoh J, Zhang SS, Barnstable CJ. Stage and gene specific signatures defined by histones H3K4me2 and H3K27me3 accompany mammalian retina maturation in vivo. Plos One. 7: e46867. PMID 23056497 DOI: 10.1371/journal.pone.0046867  0.44
2012 DeWan AT, Egan KB, Hellenbrand K, Sorrentino K, Pizzoferrato N, Walsh KM, Bracken MB. Whole-exome sequencing of a pedigree segregating asthma. Bmc Medical Genetics. 13: 95. PMID 23046476 DOI: 10.1186/1471-2350-13-95  0.44
2012 Zhao L, Dewan AT, Bracken MB. Association of maternal AGTR1 polymorphisms and preeclampsia: a systematic review and meta-analysis. 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. 25: 2676-80. PMID 22758920 DOI: 10.3109/14767058.2012.708370  0.44
2012 Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT. Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. Bmc Pregnancy and Childbirth. 12: 61. PMID 22748001 DOI: 10.1186/1471-2393-12-61  0.44
2012 Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/journal.pone.0029848  0.44
2011 Murk W, Walsh K, Hsu LI, Zhao L, Bracken MB, Dewan AT. Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthma. Human Heredity. 71: 97-105. PMID 21734400 DOI: 10.1159/000319536  0.44
2011 Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, ... Dewan AT, et al. A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocrine-Related Cancer. 18: 171-80. PMID 21139019 DOI: 10.1677/ERC-10-0248  0.44
2010 DeWan AT, Triche EW, Xu X, Hsu LI, Zhao C, Belanger K, Hellenbrand K, Willis-Owen SA, Moffatt M, Cookson WO, Himes BE, Weiss ST, Gauderman WJ, Baurley JW, Gilliland F, et al. PDE11A associations with asthma: results of a genome-wide association scan. The Journal of Allergy and Clinical Immunology. 126: 871-873.e9. PMID 20920776 DOI: 10.1016/j.jaci.2010.06.051  0.44
2010 DeWan AT. Five classic articles in genetic epidemiology. The Yale Journal of Biology and Medicine. 83: 87-90. PMID 20589189  0.44
2010 Walsh KM, Bracken MB, Murk WK, Hoh J, Dewan AT. Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutation Research. 690: 89-94. PMID 20553737 DOI: 10.1016/j.mrfmmm.2010.05.005  0.44
2004 Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, et al. X-linked high myopia associated with cone dysfunction. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 897-908. PMID 15197065 DOI: 10.1001/archopht.122.6.897  0.44
2003 Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJH, Friderici KH. Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) American Journal of Human Genetics. 73: 1082-1091. PMID 13680526 DOI: 10.1086/379286  0.44
2003 DeWan AT, Parrado AR, Leal SM. A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval Clinical Genetics. 63: 39-45. PMID 12519370 DOI: 10.1034/j.1399-0004.2003.630106.x  0.44
2002 DeWan AT, Parrado AR, Matise TC, Leal SM. Map error reduction: using genetic and sequence-based physical maps to order closely linked markers. Human Heredity. 54: 34-44. PMID 12446985 DOI: 10.1159/000066697  0.44
2002 DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study. American Journal of Human Genetics. 71: 204-5. PMID 12068377 DOI: 10.1086/340730  0.44
2002 DeWan AT, Parrado AR, Matise TC, Leal SM. The map problem: a comparison of genetic and sequence-based physical maps. American Journal of Human Genetics. 70: 101-7. PMID 11706388 DOI: 10.1086/324774  0.44
2001 Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Human Molecular Genetics. 10: 2501-8. PMID 11709537  0.44
2001 Young TL, Atwood LD, Ronan SM, Dewan AT, Alvear AB, Peterson J, Holleschau A, King RA. Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis. Ophthalmic Genetics. 22: 69-75. PMID 11449316 DOI: 10.1076/opge.22.2.69.2233  0.44
2001 DeWan AT, Arnett DK, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt J. A genome scan for renal function among hypertensives: The HyperGEN study American Journal of Human Genetics. 68: 136-144. PMID 11115379 DOI: 10.1086/316927  0.44
2000 Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN). Ophthalmic Genetics. 21: 227-33. PMID 11135493 DOI: 10.1076/1381-6810(200012)21:4;1-H;FT227  0.44
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