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Items: 1 to 50 of 228

1.

Pilot GWAS of caries in African-Americans shows genetic heterogeneity.

Orlova E, Carlson JC, Lee MK, Feingold E, McNeil DW, Crout RJ, Weyant RJ, Marazita ML, Shaffer JR.

BMC Oral Health. 2019 Sep 18;19(1):215. doi: 10.1186/s12903-019-0904-4.

2.

The haptoglobin 2-2 genotype is associated with cardiac autonomic neuropathy in type 1 diabetes: the RETRO HDLc study.

Ju J, Tomaszewski EL, Orchard TJ, Evans RW, Feingold E, Costacou T.

Acta Diabetol. 2019 Sep 16. doi: 10.1007/s00592-019-01422-6. [Epub ahead of print]

PMID:
31529337
3.

Gene Expression and Cardiometabolic Phenotypes of Vitamin D-Deficient Overweight and Obese Black Children.

Rajakumar K, Yan Q, Khalid AT, Feingold E, Vallejo AN, Demirci FY, Kamboh MI.

Nutrients. 2019 Aug 28;11(9). pii: E2016. doi: 10.3390/nu11092016.

4.

Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population.

Aslam MM, John P, Fan KH, Bhatti A, Jahangir S, Feingold E, Demirci FY, Kamboh MI.

BMC Res Notes. 2019 Aug 27;12(1):544. doi: 10.1186/s13104-019-4590-8.

5.

Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome.

Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, Wood BL, Carroll WL, Raetz EA, Feingold E, Devidas M, Barcellos LF, Hansen HM, Morimoto L, Kang AY, Smirnov I, Healy J, Laverdière C, Sinnett D, Taub JW, Birch JM, Thompson P, Spector LG, Pombo-de-Oliveira MS, DeWan AT, Mullighan CG, Hunger SP, Pui CH, Loh ML MD, Zwick ME, Metayer C, Ma X, Mueller BA, Sherman SL, Wiemels JL, Relling MV, Yang JJ, Lupo PJ, Rabin KR.

Blood. 2019 Jul 26. pii: blood.2018890764. doi: 10.1182/blood.2018890764. [Epub ahead of print]

PMID:
31350265
6.

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals.

Carlson JC, Anand D, Butali A, Buxo CJ, Christensen K, Deleyiannis F, Hecht JT, Moreno LM, Orioli IM, Padilla C, Shaffer JR, Vieira AR, Wehby GL, Weinberg SM, Murray JC, Beaty TH, Saadi I, Lachke SA, Marazita ML, Feingold E, Leslie EJ.

Genet Epidemiol. 2019 Sep;43(6):704-716. doi: 10.1002/gepi.22214. Epub 2019 Jun 6.

PMID:
31172578
7.

Predictors of dental care utilization in north-central Appalachia in the USA.

Chen M, Wright CD, Tokede O, Yansane A, Montasem A, Kalenderian E, Beaty TH, Feingold E, Shaffer JR, Crout RJ, Neiswanger K, Weyant RJ, Marazita ML, McNeil DW.

Community Dent Oral Epidemiol. 2019 Aug;47(4):283-290. doi: 10.1111/cdoe.12453. Epub 2019 Apr 17.

PMID:
30993747
8.

Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.

Kamboh MI, Fan KH, Yan Q, Beer JC, Snitz BE, Wang X, Chang CH, Demirci FY, Feingold E, Ganguli M.

Neurobiol Aging. 2019 Mar 11. pii: S0197-4580(19)30074-0. doi: 10.1016/j.neurobiolaging.2019.02.024. [Epub ahead of print]

PMID:
30954325
9.

Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups.

Pirim D, Radwan ZH, Wang X, Niemsiri V, Hokanson JE, Hamman RF, Feingold E, Bunker CH, Demirci FY, Kamboh MI.

PLoS One. 2019 Mar 26;14(3):e0214060. doi: 10.1371/journal.pone.0214060. eCollection 2019.

10.

Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.

Shaffer JR, LeClair J, Carlson JC, Feingold E, Buxó CJ, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Murray JC, Weinberg SM, Marazita ML, Leslie EJ.

Am J Med Genet A. 2019 Mar;179(3):467-474. doi: 10.1002/ajmg.a.61002. Epub 2018 Dec 24.

PMID:
30582786
11.

Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project.

Rosser TC, Edgin JO, Capone GT, Hamilton DR, Allen EG, Dooley KJ, Anand P, Strang JF, Armour AC, Frank-Crawford MA, Channell MM, Pierpont EI, Feingold E, Maslen CL, Reeves RH, Sherman SL.

Am J Intellect Dev Disabil. 2018 Nov;123(6):514-528. doi: 10.1352/1944-7558-123.6.514.

PMID:
30421968
12.

Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.

Indencleef K, Roosenboom J, Hoskens H, White JD, Shriver MD, Richmond S, Peeters H, Feingold E, Marazita ML, Shaffer JR, Weinberg SM, Hens G, Claes P.

Front Genet. 2018 Oct 25;9:502. doi: 10.3389/fgene.2018.00502. eCollection 2018.

13.

SNPs Associated With Testosterone Levels Influence Human Facial Morphology.

Roosenboom J, Indencleef K, Lee MK, Hoskens H, White JD, Liu D, Hecht JT, Wehby GL, Moreno LM, Hodges-Simeon C, Feingold E, Marazita ML, Richmond S, Shriver MD, Claes P, Shaffer JR, Weinberg SM.

Front Genet. 2018 Oct 23;9:497. doi: 10.3389/fgene.2018.00497. eCollection 2018.

14.

Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging.

Yan Q, Nho K, Del-Aguila JL, Wang X, Risacher SL, Fan KH, Snitz BE, Aizenstein HJ, Mathis CA, Lopez OL, Demirci FY, Feingold E, Klunk WE, Saykin AJ; Alzheimer’s Disease Neuroimaging Initiative (ADNI), Cruchaga C, Kamboh MI.

Mol Psychiatry. 2018 Oct 25. doi: 10.1038/s41380-018-0246-7. [Epub ahead of print]

15.

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.

Carlson JC, Nidey NL, Butali A, Buxo CJ, Christensen K, Deleyiannis FW, Hecht JT, Field LL, Moreno-Uribe LM, Orioli IM, Poletta FA, Padilla C, Vieira AR, Weinberg SM, Wehby GL, Feingold E, Murray JC, Marazita ML, Leslie EJ.

Genet Epidemiol. 2018 Oct;42(7):664-672. doi: 10.1002/gepi.22158. Epub 2018 Sep 11.

16.

Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology.

Howe LJ, Lee MK, Sharp GC, Davey Smith G, St Pourcain B, Shaffer JR, Ludwig KU, Mangold E, Marazita ML, Feingold E, Zhurov A, Stergiakouli E, Sandy J, Richmond S, Weinberg SM, Hemani G, Lewis SJ.

PLoS Genet. 2018 Aug 1;14(8):e1007501. doi: 10.1371/journal.pgen.1007501. eCollection 2018 Aug.

17.

Statistics for X-chromosome associations.

Özbek U, Lin HM, Lin Y, Weeks DE, Chen W, Shaffer JR, Purcell SM, Feingold E.

Genet Epidemiol. 2018 Sep;42(6):539-550. doi: 10.1002/gepi.22132. Epub 2018 Jun 13.

18.

Novel caries loci in children and adults implicated by genome-wide analysis of families.

Govil M, Mukhopadhyay N, Weeks DE, Feingold E, Shaffer JR, Levy SM, Vieira AR, Slayton RL, McNeil DW, Weyant RJ, Crout RJ, Marazita ML.

BMC Oral Health. 2018 Jun 1;18(1):98. doi: 10.1186/s12903-018-0559-6.

19.

GWAS reveals loci associated with velopharyngeal dysfunction.

Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, Hecht JT, Padilla C, Deleyiannis FWB, Buxo CJ, Feingold E, Leslie EJ, Shaffer JR, Weinberg SM, Marazita ML.

Sci Rep. 2018 May 31;8(1):8470. doi: 10.1038/s41598-018-26880-w.

20.

Apixaban decreases brain thrombin activity in a male mouse model of acute ischemic stroke.

Bushi D, Chapman J, Wohl A, Stein ES, Feingold E, Tanne D.

J Neurosci Res. 2018 Aug;96(8):1406-1411. doi: 10.1002/jnr.24253. Epub 2018 May 14.

PMID:
29761540
21.

Mapping genetic variants for cranial vault shape in humans.

Roosenboom J, Lee MK, Hecht JT, Heike CL, Wehby GL, Christensen K, Feingold E, Marazita ML, Maga AM, Shaffer JR, Weinberg SM.

PLoS One. 2018 Apr 26;13(4):e0196148. doi: 10.1371/journal.pone.0196148. eCollection 2018.

22.

Genome-wide mapping of global-to-local genetic effects on human facial shape.

Claes P, Roosenboom J, White JD, Swigut T, Sero D, Li J, Lee MK, Zaidi A, Mattern BC, Liebowitz C, Pearson L, González T, Leslie EJ, Carlson JC, Orlova E, Suetens P, Vandermeulen D, Feingold E, Marazita ML, Shaffer JR, Wysocka J, Shriver MD, Weinberg SM.

Nat Genet. 2018 Mar;50(3):414-423. doi: 10.1038/s41588-018-0057-4. Epub 2018 Feb 19.

23.

The Association between SNPs and a Quantitative Trait: Power Calculation.

Delongchamp R, Faramawi MF, Feingold E, Chung D, Abouelenein S.

Eur J Environ Public Health. 2018;2(2). pii: 10. doi: 10.20897/ejeph/3925. Epub 2018 Oct 16.

24.

Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.

Shaffer JR, Li J, Lee MK, Roosenboom J, Orlova E, Adhikari K; 23andMe Research Team, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, González-José R, Pfeffer PE, Wollenschlaeger CA, Hecht JT, Wehby GL, Moreno LM, Ding A, Jin L, Yang Y, Carlson JC, Leslie EJ, Feingold E, Marazita ML, Hinds DA, Cox TC, Wang S, Ruiz-Linares A, Weinberg SM.

Am J Hum Genet. 2017 Dec 7;101(6):913-924. doi: 10.1016/j.ajhg.2017.10.001. Epub 2017 Nov 30.

25.

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.

Carlson JC, Standley J, Petrin A, Shaffer JR, Butali A, Buxó CJ, Castilla E, Christensen K, Deleyiannis FW, Hecht JT, Field LL, Garidkhuu A, Moreno Uribe LM, Nagato N, Orioli IM, Padilla C, Poletta F, Suzuki S, Vieira AR, Wehby GL, Weinberg SM, Beaty TH, Feingold E, Murray JC, Marazita ML, Leslie EJ.

Genet Epidemiol. 2017 Dec;41(8):887-897. doi: 10.1002/gepi.22090. Epub 2017 Nov 10.

26.

Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births.

Bhaumik P, Ghosh P, Ghosh S, Feingold E, Ozbek U, Sarkar B, Dey SK.

Genet Mol Biol. 2017 Jul-Sep;40(3):577-585. doi: 10.1590/1678-4685-GMB-2016-0138. Epub 2017 Jul 31.

27.

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.

Carlson JC, Taub MA, Feingold E, Beaty TH, Murray JC, Marazita ML, Leslie EJ.

Birth Defects Res. 2017 Jul 17;109(13):1030-1038. doi: 10.1002/bdr2.23605.

28.

Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin.

Oliver TR, Middlebrooks C, Harden A, Scott N, Johnson B, Jones J, Walker C, Wilkerson C, Saffold SH, Akinseye A, Smith T, Feingold E, Sherman SL.

J Down Syndr Chromosom Abnorm. 2016 Dec;2(2). pii: 115. doi: 10.4172/2472-1115.1000115. Epub 2016 Nov 23.

29.

A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.

Randall CL, Wright CD, Chernus JM, McNeil DW, Feingold E, Crout RJ, Neiswanger K, Weyant RJ, Shaffer JR, Marazita ML.

Pain Res Manag. 2017;2017:7375468. doi: 10.1155/2017/7375468. Epub 2017 Jun 15.

30.

A Linear Temporal Increase in Thrombin Activity and Loss of Its Receptor in Mouse Brain following Ischemic Stroke.

Bushi D, Stein ES, Golderman V, Feingold E, Gera O, Chapman J, Tanne D.

Front Neurol. 2017 Apr 10;8:138. doi: 10.3389/fneur.2017.00138. eCollection 2017.

31.

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

Lee MK, Shaffer JR, Leslie EJ, Orlova E, Carlson JC, Feingold E, Marazita ML, Weinberg SM.

PLoS One. 2017 Apr 25;12(4):e0176566. doi: 10.1371/journal.pone.0176566. eCollection 2017.

32.

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

Leslie EJ, Carlson JC, Shaffer JR, Buxó CJ, Castilla EE, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Feingold E, Weinberg SM, Murray JC, Marazita ML.

Am J Med Genet A. 2017 Jun;173(6):1531-1538. doi: 10.1002/ajmg.a.38210. Epub 2017 Apr 19.

33.

Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries.

Lewis DD, Shaffer JR, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML.

Int J Dent. 2017;2017:8465125. doi: 10.1155/2017/8465125. Epub 2017 Feb 28.

34.

Protease Activated Receptor 2 (PAR2) Induces Long-Term Depression in the Hippocampus through Transient Receptor Potential Vanilloid 4 (TRPV4).

Shavit-Stein E, Artan-Furman A, Feingold E, Ben Shimon M, Itzekson-Hayosh Z, Chapman J, Vlachos A, Maggio N.

Front Mol Neurosci. 2017 Mar 2;10:42. doi: 10.3389/fnmol.2017.00042. eCollection 2017.

35.

Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus.

Demirci FY, Wang X, Morris DL, Feingold E, Bernatsky S, Pineau C, Clarke A, Ramsey-Goldman R, Manzi S, Vyse TJ, Kamboh MI.

J Med Genet. 2017 Jun;54(6):381-389. doi: 10.1136/jmedgenet-2016-104247. Epub 2017 Mar 13.

36.

Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries.

Eckert S, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR.

J Hum Genet. 2017 Apr;62(4):491-496. doi: 10.1038/jhg.2016.161. Epub 2017 Jan 19.

37.

Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.

Leslie EJ, Carlson JC, Shaffer JR, Butali A, Buxó CJ, Castilla EE, Christensen K, Deleyiannis FW, Leigh Field L, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Feingold E, Weinberg SM, Murray JC, Beaty TH, Marazita ML.

Hum Genet. 2017 Mar;136(3):275-286. doi: 10.1007/s00439-016-1754-7. Epub 2017 Jan 4.

38.

Genome-Wide Association Study of Meiotic Recombination Phenotypes.

Begum F, Chowdhury R, Cheung VG, Sherman SL, Feingold E.

G3 (Bethesda). 2016 Dec 7;6(12):3995-4007. doi: 10.1534/g3.116.035766.

39.

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.

Shaffer JR, Orlova E, Lee MK, Leslie EJ, Raffensperger ZD, Heike CL, Cunningham ML, Hecht JT, Kau CH, Nidey NL, Moreno LM, Wehby GL, Murray JC, Laurie CA, Laurie CC, Cole J, Ferrara T, Santorico S, Klein O, Mio W, Feingold E, Hallgrimsson B, Spritz RA, Marazita ML, Weinberg SM.

PLoS Genet. 2016 Aug 25;12(8):e1006149. doi: 10.1371/journal.pgen.1006149. eCollection 2016 Aug.

40.

Structural and genomic variation in preterm birth.

Uzun A, Sahin Y, Schuster JS, Zheng X, Ryckman K, Feingold E, Padbury J.

Pediatr Res. 2016 Dec;80(6):829-836. doi: 10.1038/pr.2016.152. Epub 2016 Jul 24.

41.

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

Leslie EJ, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, Neiswanger K, Lidral AC, Valencia-Ramirez LC, Lopez-Palacio AM, Valencia DR, Arcos-Burgos M, Czeizel AE, Field LL, Padilla CD, Cutiongco-de la Paz EM, Deleyiannis F, Christensen K, Munger RG, Lie RT, Wilcox A, Romitti PA, Castilla EE, Mereb JC, Poletta FA, Orioli IM, Carvalho FM, Hecht JT, Blanton SH, Buxó CJ, Butali A, Mossey PA, Adeyemo WL, James O, Braimah RO, Aregbesola BS, Eshete MA, Abate F, Koruyucu M, Seymen F, Ma L, de Salamanca JE, Weinberg SM, Moreno L, Murray JC, Marazita ML.

Hum Mol Genet. 2016 Jul 1;25(13):2862-2872. Epub 2016 Mar 30.

42.

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

Leslie EJ, Liu H, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, Neiswanger K, Standley J, Czeizel AE, Deleyiannis F, Christensen K, Munger RG, Lie RT, Wilcox A, Romitti PA, Field LL, Padilla CD, Cutiongco-de la Paz EM, Lidral AC, Valencia-Ramirez LC, Lopez-Palacio AM, Valencia DR, Arcos-Burgos M, Castilla EE, Mereb JC, Poletta FA, Orioli IM, Carvalho FM, Hecht JT, Blanton SH, Buxó CJ, Butali A, Mossey PA, Adeyemo WL, James O, Braimah RO, Aregbesola BS, Eshete MA, Deribew M, Koruyucu M, Seymen F, Ma L, de Salamanca JE, Weinberg SM, Moreno L, Cornell RA, Murray JC, Marazita ML.

Am J Hum Genet. 2016 Apr 7;98(4):744-54. doi: 10.1016/j.ajhg.2016.02.014. Epub 2016 Mar 24.

43.

A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information.

Zeng Z, Weeks DE, Chen W, Mukhopadhyay N, Feingold E.

Genet Epidemiol. 2016 Feb;40(2):161-71. doi: 10.1002/gepi.21948. Epub 2015 Dec 28.

44.

Regionally Smoothed Meta-Analysis Methods for GWAS Datasets.

Begum F, Sharker MH, Sherman SL, Tseng GC, Feingold E.

Genet Epidemiol. 2016 Feb;40(2):154-60. doi: 10.1002/gepi.21949. Epub 2015 Dec 28.

45.

Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers.

Özbek U, Feingold E, Weeks DE.

Hum Hered. 2015;80(2):79-89. doi: 10.1159/000441279. Epub 2015 Nov 28.

PMID:
26613255
46.

Maternal Telomere Length and Risk of Down Syndrome: Epidemiological Impact of Smokeless Chewing Tobacco and Oral Contraceptive on Segregation of Chromosome 21.

Ray A, Hong CS, Feingold E, Ghosh P, Ghosh P, Bhaumik P, Dey S, Ghosh S.

Public Health Genomics. 2016;19(1):11-8. doi: 10.1159/000439245. Epub 2015 Oct 7.

47.

Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry.

Demirci FY, Wang X, Kelly JA, Morris DL, Barmada MM, Feingold E, Kao AH, Sivils KL, Bernatsky S, Pineau C, Clarke AE, Ramsey-Goldman R, Vyse TJ, Gaffney PM, Manzi S, Kamboh MI.

Arthritis Rheumatol. 2016 Jan;68(1):174-83. doi: 10.1002/art.39403.

48.

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.

Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME.

G3 (Bethesda). 2015 Jul 20;5(10):1961-71. doi: 10.1534/g3.115.019943.

49.

Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia.

Shaffer JR, Leslie EJ, Feingold E, Govil M, McNeil DW, Crout RJ, Weyant RJ, Marazita ML.

Int J Dent. 2015;2015:938213. doi: 10.1155/2015/938213. Epub 2015 May 27.

50.

Genome-wide copy-number variation study of psychosis in Alzheimer's disease.

Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E.

Transl Psychiatry. 2015 Jun 2;5:e574. doi: 10.1038/tp.2015.64.

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