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Items: 1 to 50 of 211

1.

Statistics for X-chromosome associations.

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

Genet Epidemiol. 2018 Jun 13. doi: 10.1002/gepi.22132. [Epub ahead of print]

PMID:
29900581
2.

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.

3.

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.

4.

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
5.

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.

6.

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.

PMID:
29459680
7.

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.

8.

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.

PMID:
29124805
9.

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.

10.

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.

11.

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.

12.

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.

13.

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.

14.

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.

15.

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.

16.

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.

17.

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.

18.

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.

19.

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.

20.

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.

21.

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.

22.

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.

23.

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.

24.

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.

25.

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.

26.

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.

27.

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.

28.

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
29.

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.

30.

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.

31.

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.

32.

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.

33.

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.

34.

Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3).

Weinreb NJ, Finegold DN, Feingold E, Zeng Z, Rosenbloom BE, Shankar SP, Amato D.

Orphanet J Rare Dis. 2015 May 22;10:64. doi: 10.1186/s13023-015-0280-3.

35.

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate.

Wolf ZT, Brand HA, Shaffer JR, Leslie EJ, Arzi B, Willet CE, Cox TC, McHenry T, Narayan N, Feingold E, Wang X, Sliskovic S, Karmi N, Safra N, Sanchez C, Deleyiannis FW, Murray JC, Wade CM, Marazita ML, Bannasch DL.

PLoS Genet. 2015 Mar 23;11(3):e1005059. doi: 10.1371/journal.pgen.1005059. eCollection 2015 Mar.

36.

Effect of body mass index and albumin on mortality rates for adult African-American hemodialysis patients.

Feingold E, Adams J, Penprase B, Tubie B.

J Am Assoc Nurse Pract. 2015 Nov;27(11):637-45. doi: 10.1002/2327-6924.12236. Epub 2015 Mar 11.

PMID:
25761048
37.

Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.

Wang X, Lopez O, Sweet RA, Becker JT, DeKosky ST, Barmada MM, Feingold E, Demirci FY, Kamboh MI.

J Alzheimers Dis. 2015;45(2):651-8.

38.

A comparative encyclopedia of DNA elements in the mouse genome.

Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, Rynes E, Kirilusha A, Marinov GK, Williams BA, Trout D, Amrhein H, Fisher-Aylor K, Antoshechkin I, DeSalvo G, See LH, Fastuca M, Drenkow J, Zaleski C, Dobin A, Prieto P, Lagarde J, Bussotti G, Tanzer A, Denas O, Li K, Bender MA, Zhang M, Byron R, Groudine MT, McCleary D, Pham L, Ye Z, Kuan S, Edsall L, Wu YC, Rasmussen MD, Bansal MS, Kellis M, Keller CA, Morrissey CS, Mishra T, Jain D, Dogan N, Harris RS, Cayting P, Kawli T, Boyle AP, Euskirchen G, Kundaje A, Lin S, Lin Y, Jansen C, Malladi VS, Cline MS, Erickson DT, Kirkup VM, Learned K, Sloan CA, Rosenbloom KR, Lacerda de Sousa B, Beal K, Pignatelli M, Flicek P, Lian J, Kahveci T, Lee D, Kent WJ, Ramalho Santos M, Herrero J, Notredame C, Johnson A, Vong S, Lee K, Bates D, Neri F, Diegel M, Canfield T, Sabo PJ, Wilken MS, Reh TA, Giste E, Shafer A, Kutyavin T, Haugen E, Dunn D, Reynolds AP, Neph S, Humbert R, Hansen RS, De Bruijn M, Selleri L, Rudensky A, Josefowicz S, Samstein R, Eichler EE, Orkin SH, Levasseur D, Papayannopoulou T, Chang KH, Skoultchi A, Gosh S, Disteche C, Treuting P, Wang Y, Weiss MJ, Blobel GA, Cao X, Zhong S, Wang T, Good PJ, Lowdon RF, Adams LB, Zhou XQ, Pazin MJ, Feingold EA, Wold B, Taylor J, Mortazavi A, Weissman SM, Stamatoyannopoulos JA, Snyder MP, Guigo R, Gingeras TR, Gilbert DM, Hardison RC, Beer MA, Ren B; Mouse ENCODE Consortium.

Nature. 2014 Nov 20;515(7527):355-64. doi: 10.1038/nature13992.

39.

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease.

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

PLoS One. 2014 Nov 7;9(11):e111462. doi: 10.1371/journal.pone.0111462. eCollection 2014.

40.

Effects of enamel matrix genes on dental caries are moderated by fluoride exposures.

Shaffer JR, Carlson JC, Stanley BO, 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.

Hum Genet. 2015 Feb;134(2):159-67. doi: 10.1007/s00439-014-1504-7. Epub 2014 Nov 6.

41.

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects.

Redig JK, Fouad GT, Babcock D, Reshey B, Feingold E, Reeves RH, Maslen CL.

AIMS Genet. 2014;1(1):1-19.

42.

Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease.

Kellis M, Wold B, Snyder MP, Bernstein BE, Kundaje A, Marinov GK, Ward LD, Birney E, Crawford GE, Dekker J, Dunham I, Elnitski LL, Farnham PJ, Feingold EA, Gerstein M, Giddings MC, Gilbert DM, Gingeras TR, Green ED, Guigo R, Hubbard T, Kent J, Lieb JD, Myers RM, Pazin MJ, Ren B, Stamatoyannopoulos J, Weng Z, White KP, Hardison RC.

Proc Natl Acad Sci U S A. 2014 Aug 19;111(33):E3366. No abstract available.

43.

Comparative analysis of regulatory information and circuits across distant species.

Boyle AP, Araya CL, Brdlik C, Cayting P, Cheng C, Cheng Y, Gardner K, Hillier LW, Janette J, Jiang L, Kasper D, Kawli T, Kheradpour P, Kundaje A, Li JJ, Ma L, Niu W, Rehm EJ, Rozowsky J, Slattery M, Spokony R, Terrell R, Vafeados D, Wang D, Weisdepp P, Wu YC, Xie D, Yan KK, Feingold EA, Good PJ, Pazin MJ, Huang H, Bickel PJ, Brenner SE, Reinke V, Waterston RH, Gerstein M, White KP, Kellis M, Snyder M.

Nature. 2014 Aug 28;512(7515):453-6. doi: 10.1038/nature13668.

44.

Comparative analysis of metazoan chromatin organization.

Ho JW, Jung YL, Liu T, Alver BH, Lee S, Ikegami K, Sohn KA, Minoda A, Tolstorukov MY, Appert A, Parker SC, Gu T, Kundaje A, Riddle NC, Bishop E, Egelhofer TA, Hu SS, Alekseyenko AA, Rechtsteiner A, Asker D, Belsky JA, Bowman SK, Chen QB, Chen RA, Day DS, Dong Y, Dose AC, Duan X, Epstein CB, Ercan S, Feingold EA, Ferrari F, Garrigues JM, Gehlenborg N, Good PJ, Haseley P, He D, Herrmann M, Hoffman MM, Jeffers TE, Kharchenko PV, Kolasinska-Zwierz P, Kotwaliwale CV, Kumar N, Langley SA, Larschan EN, Latorre I, Libbrecht MW, Lin X, Park R, Pazin MJ, Pham HN, Plachetka A, Qin B, Schwartz YB, Shoresh N, Stempor P, Vielle A, Wang C, Whittle CM, Xue H, Kingston RE, Kim JH, Bernstein BE, Dernburg AF, Pirrotta V, Kuroda MI, Noble WS, Tullius TD, Kellis M, MacAlpine DM, Strome S, Elgin SC, Liu XS, Lieb JD, Ahringer J, Karpen GH, Park PJ.

Nature. 2014 Aug 28;512(7515):449-52. doi: 10.1038/nature13415.

45.

Comparative analysis of the transcriptome across distant species.

Gerstein MB, Rozowsky J, Yan KK, Wang D, Cheng C, Brown JB, Davis CA, Hillier L, Sisu C, Li JJ, Pei B, Harmanci AO, Duff MO, Djebali S, Alexander RP, Alver BH, Auerbach R, Bell K, Bickel PJ, Boeck ME, Boley NP, Booth BW, Cherbas L, Cherbas P, Di C, Dobin A, Drenkow J, Ewing B, Fang G, Fastuca M, Feingold EA, Frankish A, Gao G, Good PJ, Guigó R, Hammonds A, Harrow J, Hoskins RA, Howald C, Hu L, Huang H, Hubbard TJ, Huynh C, Jha S, Kasper D, Kato M, Kaufman TC, Kitchen RR, Ladewig E, Lagarde J, Lai E, Leng J, Lu Z, MacCoss M, May G, McWhirter R, Merrihew G, Miller DM, Mortazavi A, Murad R, Oliver B, Olson S, Park PJ, Pazin MJ, Perrimon N, Pervouchine D, Reinke V, Reymond A, Robinson G, Samsonova A, Saunders GI, Schlesinger F, Sethi A, Slack FJ, Spencer WC, Stoiber MH, Strasbourger P, Tanzer A, Thompson OA, Wan KH, Wang G, Wang H, Watkins KL, Wen J, Wen K, Xue C, Yang L, Yip K, Zaleski C, Zhang Y, Zheng H, Brenner SE, Graveley BR, Celniker SE, Gingeras TR, Waterston R.

Nature. 2014 Aug 28;512(7515):445-8. doi: 10.1038/nature13424.

46.

Obesity in urban women: associations with sleep and sleepiness, fatigue and activity.

Jarosz PA, Davis JE, Yarandi HN, Farkas R, Feingold E, Shippings SH, Smith AL, Williams D.

Womens Health Issues. 2014 Jul-Aug;24(4):e447-54. doi: 10.1016/j.whi.2014.04.005.

PMID:
24981402
47.

An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.

Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL.

PLoS One. 2014 Jun 13;9(6):e99560. doi: 10.1371/journal.pone.0099560. eCollection 2014.

48.

Genetic Association of MPPED2 and ACTN2 with Dental Caries.

Stanley BO, 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 Dent Res. 2014 Jul;93(7):626-32. doi: 10.1177/0022034514534688. Epub 2014 May 8.

49.

Defining functional DNA elements in the human genome.

Kellis M, Wold B, Snyder MP, Bernstein BE, Kundaje A, Marinov GK, Ward LD, Birney E, Crawford GE, Dekker J, Dunham I, Elnitski LL, Farnham PJ, Feingold EA, Gerstein M, Giddings MC, Gilbert DM, Gingeras TR, Green ED, Guigo R, Hubbard T, Kent J, Lieb JD, Myers RM, Pazin MJ, Ren B, Stamatoyannopoulos JA, Weng Z, White KP, Hardison RC.

Proc Natl Acad Sci U S A. 2014 Apr 29;111(17):6131-8. doi: 10.1073/pnas.1318948111. Epub 2014 Apr 21. Review.

50.

Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.

Zeng Z, Feingold E, Wang X, Weeks DE, Lee M, Cuenco DT, Broffitt B, Weyant RJ, Crout R, McNeil DW, Levy SM, Marazita ML, Shaffer JR.

Caries Res. 2014;48(4):330-8.

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