| Year |
Citation |
Score |
| 2023 |
Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Sherva RM, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311 |
0.379 |
|
| 2022 |
Sherva R, Zhang R, Sahelijo N, Jun G, Anglin T, Chanfreau C, Cho K, Fonda JR, Gaziano JM, Harrington KM, Ho YL, Kremen WS, Litkowski E, Lynch J, Neale Z, et al. African ancestry GWAS of dementia in a large military cohort identifies significant risk loci. Molecular Psychiatry. PMID 36543923 DOI: 10.1038/s41380-022-01890-3 |
0.353 |
|
| 2022 |
Gaddis N, Mathur R, Marks J, Zhou L, Quach B, Waldrop A, Levran O, Agrawal A, Randesi M, Adelson M, Jeffries PW, Martin NG, Degenhardt L, Montgomery GW, Wetherill L, ... ... Sherva R, et al. Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Scientific Reports. 12: 16873. PMID 36207451 DOI: 10.1038/s41598-022-21003-y |
0.354 |
|
| 2020 |
Sherva R, Gross A, Mukherjee S, Koesterer R, Amouyel P, Bellenguez C, Dufouil C, Bennett DA, Chibnik L, Cruchaga C, Del-Aguila J, Farrer LA, Mayeux R, Munsie L, Winslow A, et al. Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32573913 DOI: 10.1002/Alz.12106 |
0.392 |
|
| 2020 |
Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, ... ... Sherva R, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology. e12880. PMID 32064741 DOI: 10.1111/Adb.12880 |
0.345 |
|
| 2020 |
Cox JW, Sherva RM, Lunetta KL, Johnson EC, Martin NG, Degenhardt L, Agrawal A, Nelson EC, Kranzler HR, Gelernter J, Farrer LA. Genome-Wide Association Study of Opioid Cessation. Journal of Clinical Medicine. 9. PMID 31936517 DOI: 10.3390/Jcm9010180 |
0.412 |
|
| 2019 |
Marees AT, Gamazon ER, Gerring Z, Vorspan F, Fingal J, van den Brink W, Smit DJA, Verweij KJH, Kranzler HR, Sherva R, Farrer L, Gelernter J, Derks EM. Post-GWAS analysis of six substance use traits improves the identification and functional interpretation of genetic risk loci. Drug and Alcohol Dependence. 107703. PMID 31785998 DOI: 10.1016/J.Drugalcdep.2019.107703 |
0.394 |
|
| 2019 |
Chen J, Loukola A, Gillespie NA, Peterson R, Jia P, Riley B, Maes H, Dick DM, Kendler KS, Damaj MI, Miles MF, Zhao Z, Li MD, Vink JM, Minica CC, ... ... Sherva R, et al. Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. PMID 31294817 DOI: 10.1093/Ntr/Ntz099 |
0.337 |
|
| 2019 |
Zhou H, Polimanti R, Yang B, Wang Q, Han S, Sherva R, Nunez Y, Zhao H, Farrer L, Kranzler H, Gelernter J. Genome-Wide Association Study Of Comorbid Alcohol Dependence And Major Depression European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.338 |
0.389 |
|
| 2019 |
Gelernter J, Sherva R, Zhao H, Kranzler H, Farrer L. Initial Results From An Opioid Dependence Whole Exome Sequencing Study European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.056 |
0.407 |
|
| 2018 |
Walters RK, Polimanti R, Johnson EC, McClintick JN, Adams MJ, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Chou YL, ... ... Sherva R, et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience. 21: 1656-1669. PMID 30482948 DOI: 10.1038/S41593-018-0275-1 |
0.432 |
|
| 2018 |
Minică CC, Verweij KJH, van der Most PJ, Mbarek H, Bernard M, van Eijk KR, Lind PA, Liu MZ, Maciejewski DF, Palviainen T, Sánchez-Mora C, Sherva R, Taylor M, Walters RK, Abdellaoui A, et al. GENOME-WIDE ASSOCIATION META-ANALYSIS OF AGE AT FIRST CANNABIS USE. Addiction (Abingdon, England). PMID 30003630 DOI: 10.1111/Add.14368 |
0.329 |
|
| 2018 |
Cheng Z, Zhou H, Sherva R, Farrer LA, Kranzler HR, Gelernter J. Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. Biological Psychiatry. PMID 29478698 DOI: 10.1016/J.Biopsych.2017.12.016 |
0.37 |
|
| 2018 |
Datta S, Sherva RM, De La Cruz M, Long MT, Roy P, Backman V, Chowdhury S, Roy HK. Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial Disparities. Neoplasia (New York, N.Y.). 20: 289-294. PMID 29471289 DOI: 10.1016/J.Neo.2018.01.003 |
0.367 |
|
| 2017 |
Chung J, Wang X, Maruyama T, Ma Y, Zhang X, Mez J, Sherva R, Takeyama H, Lunetta KL, Farrer LA, Jun GR. Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 29274321 DOI: 10.1016/J.Jalz.2017.11.006 |
0.386 |
|
| 2017 |
Agrawal A, Chou YL, Carey CE, Baranger DAA, Zhang B, Sherva R, Wetherill L, Kapoor M, Wang JC, Bertelsen S, Anokhin AP, Hesselbrock V, Kramer J, Lynskey MT, Meyers JL, et al. Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry. PMID 29112194 DOI: 10.1038/Mp.2017.200 |
0.455 |
|
| 2017 |
Zhou H, Polimanti R, Yang BZ, Wang Q, Han S, Sherva R, Nuñez YZ, Zhao H, Farrer LA, Kranzler HR, Gelernter J. Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. Jama Psychiatry. PMID 29071344 DOI: 10.1001/Jamapsychiatry.2017.3275 |
0.346 |
|
| 2017 |
Hancock DB, Guo Y, Reginsson GW, Gaddis NC, Lutz SM, Sherva R, Loukola A, Minica CC, Markunas CA, Han Y, Young KA, Gudbjartsson DF, Gu F, McNeil DW, Qaiser B, et al. Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Molecular Psychiatry. PMID 28972577 DOI: 10.1038/Mp.2017.193 |
0.408 |
|
| 2017 |
Sippel LM, Han S, Watkins LE, Harpaz-Rotem I, Southwick SM, Krystal JH, Olff M, Sherva R, Farrer LA, Kranzler HR, Gelernter J, Pietrzak RH. Oxytocin receptor gene polymorphisms, attachment, and PTSD: Results from the National Health and Resilience in Veterans Study. Journal of Psychiatric Research. 94: 139-147. PMID 28715704 DOI: 10.1016/J.Jpsychires.2017.07.008 |
0.366 |
|
| 2017 |
Adkins AE, Hack LM, Bigdeli TB, Williamson VS, McMichael GO, Mamdani M, Edwards A, Aliev F, Chan RF, Bhandari P, Raabe RC, Alaimo JT, Blackwell GG, Moscati AA, Poland RS, ... ... Sherva R, et al. Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-response Behaviors in Model Organisms. Alcoholism, Clinical and Experimental Research. PMID 28226201 DOI: 10.1111/Acer.13362 |
0.343 |
|
| 2017 |
Jun GR, Chung J, Mez J, Barber R, Beecham GW, Bennett DA, Buxbaum JD, Byrd GS, Carrasquillo MM, Crane PK, Cruchaga C, De Jager P, Ertekin-Taner N, Evans D, Fallin MD, ... ... Sherva R, et al. Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28183528 DOI: 10.1016/J.Jalz.2016.12.012 |
0.396 |
|
| 2017 |
Chung J, Wang X, Ma Y, Maruyama T, Kim M, Zhang X, Takeyama H, Mez J, Sherva R, Lunetta KL, Farrer LA, Jun GR. Genome-Wide Association Study Of Alzheimer Disease Endophenotypes At Preclinical And Mci Stages Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.062 |
0.385 |
|
| 2016 |
Wachman EM, Hayes MJ, Sherva R, Brown MS, Shrestha H, Logan BA, Heller NA, Nielsen DA, Farrer LA. Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity. The American Journal On Addictions. PMID 27983768 DOI: 10.1111/Ajad.12483 |
0.366 |
|
| 2016 |
Mez J, Chung J, Jun G, Kriegel J, Bourlas AP, Sherva R, Logue MW, Barnes LL, Bennett DA, Buxbaum JD, Byrd GS, Crane PK, Ertekin-Taner N, Evans D, Fallin MD, et al. Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 27770636 DOI: 10.1016/J.Jalz.2016.09.002 |
0.364 |
|
| 2016 |
Mez J, Mukherjee S, Thornton T, Fardo DW, Trittschuh E, Sutti S, Sherva R, Kauwe JS, Naj AC, Beecham GW, Gross A, Saykin AJ, Green RC, Crane PK, et al. The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable. Neurobiology of Aging. 41: 115-21. PMID 27103524 DOI: 10.1016/J.Neurobiolaging.2016.02.015 |
0.314 |
|
| 2016 |
Sherva R, Wang Q, Kranzler H, Zhao H, Koesterer R, Herman A, Farrer LA, Gelernter J. Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. Jama Psychiatry. PMID 27028160 DOI: 10.1001/Jamapsychiatry.2016.0036 |
0.361 |
|
| 2016 |
Stringer S, Minică CC, Verweij KJ, Mbarek H, Bernard M, Derringer J, van Eijk KR, Isen JD, Loukola A, Maciejewski DF, Mihailov E, van der Most PJ, Sánchez-Mora C, Roos L, Sherva R, et al. Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry. 6: e769. PMID 27023175 DOI: 10.1038/Tp.2016.36 |
0.553 |
|
| 2015 |
Hancock DB, Reginsson GW, Gaddis NC, Chen X, Saccone NL, Lutz SM, Qaiser B, Sherva R, Steinberg S, Zink F, Stacey SN, Glasheen C, Chen J, Gu F, Frederiksen BN, et al. Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence. Translational Psychiatry. 5: e651. PMID 26440539 DOI: 10.1038/Tp.2015.149 |
0.403 |
|
| 2015 |
Mbarek H, Milaneschi Y, Fedko IO, Hottenga JJ, de Moor MH, Jansen R, Gelernter J, Sherva R, Willemsen G, Boomsma DI, Penninx BW, Vink JM. The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26365420 DOI: 10.1002/Ajmg.B.32379 |
0.443 |
|
| 2015 |
Nelson EC, Agrawal A, Heath AC, Bogdan R, Sherva R, Zhang B, Al-Hasani R, Bruchas MR, Chou YL, Demers CH, Carey CE, Conley ED, Fakira AK, Farrer LA, Goate A, et al. Evidence of CNIH3 involvement in opioid dependence. Molecular Psychiatry. PMID 26239289 DOI: 10.1038/Mp.2015.102 |
0.404 |
|
| 2015 |
Wachman EM, Hayes MJ, Sherva R, Brown MS, Davis JM, Farrer LA, Nielsen DA. Variations in opioid receptor genes in neonatal abstinence syndrome. Drug and Alcohol Dependence. PMID 26233486 DOI: 10.1016/J.Drugalcdep.2015.07.001 |
0.321 |
|
| 2015 |
Xu K, Kranzler HR, Sherva R, Sartor CE, Almasy L, Koesterer R, Zhao H, Farrer LA, Gelernter J. Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans. Alcoholism, Clinical and Experimental Research. PMID 26036284 DOI: 10.1111/Acer.12751 |
0.423 |
|
| 2015 |
Gelernter J, Kranzler HR, Sherva R, Almasy L, Herman AI, Koesterer R, Zhao H, Farrer LA. Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. Biological Psychiatry. 77: 493-503. PMID 25555482 DOI: 10.1016/J.Biopsych.2014.08.025 |
0.354 |
|
| 2015 |
Del-Aguila JL, Gross AL, Sutti S, Sherva R, Mukherjee S, Crane PK, Goate A, Morris JC, Green RC, Cruchaga C. Identification of genetic variants associated with Alzheimer's disease: Progression rate Alzheimers & Dementia. 11: 487. DOI: 10.1016/J.Jalz.2015.06.552 |
0.388 |
|
| 2014 |
Levey DF, Le-Niculescu H, Frank J, Ayalew M, Jain N, Kirlin B, Learman R, Winiger E, Rodd Z, Shekhar A, Schork N, Kiefer F, Kiefe F, Wodarz N, Müller-Myhsok B, ... ... Sherva R, et al. Genetic risk prediction and neurobiological understanding of alcoholism. Translational Psychiatry. 4: e391. PMID 24844177 DOI: 10.1038/Tp.2014.29 |
0.35 |
|
| 2014 |
Gelernter J, Kranzler HR, Sherva R, Almasy L, Koesterer R, Smith AH, Anton R, Preuss UW, Ridinger M, Rujescu D, Wodarz N, Zill P, Zhao H, Farrer LA. Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. Molecular Psychiatry. 19: 41-9. PMID 24166409 DOI: 10.1038/Mp.2013.145 |
0.45 |
|
| 2014 |
Gelernter J, Kranzler HR, Sherva R, Koesterer R, Almasy L, Zhao H, Farrer LA. Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways. Biological Psychiatry. 76: 66-74. PMID 24143882 DOI: 10.1016/J.Biopsych.2013.08.034 |
0.433 |
|
| 2014 |
Gelernter J, Sherva R, Koesterer R, Almasy L, Zhao H, Kranzler HR, Farrer L. Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. Molecular Psychiatry. 19: 717-23. PMID 23958962 DOI: 10.1038/Mp.2013.99 |
0.447 |
|
| 2014 |
Sherva R, Tripodis Y, Bennett DA, Chibnik LB, Crane PK, de Jager PL, Farrer LA, Saykin AJ, Shulman JM, Naj A, Green RC. Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 45-52. PMID 23535033 DOI: 10.1016/J.Jalz.2013.01.008 |
0.374 |
|
| 2013 |
Xie G, Roshandel D, Sherva R, Monach PA, Lu EY, Kung T, Carrington K, Zhang SS, Pulit SL, Ripke S, Carette S, Dellaripa PF, Edberg JC, Hoffman GS, Khalidi N, et al. Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis. Arthritis and Rheumatism. 65: 2457-68. PMID 23740775 DOI: 10.1002/Art.38036 |
0.428 |
|
| 2013 |
Xie G, Roschandel D, Sherva R, Monach P, Lu Y, Kung T, Carrington K, Carette S, Dellaripa P, Edberg J, Hoffman G, Khalidi N, Langford C, Mahr A, St. Clair E, et al. Granulomatosis with polyangiitis (Wegener's) is associated with HLA-DPB1*04 and EMA6A gene variants. Evidence from a genome-wide analysis La Presse MéDicale. 42: 668. DOI: 10.1016/J.Lpm.2013.02.042 |
0.417 |
|
| 2013 |
Chung J, Sherva R, Koesterer R, Haines J, Pericak-Vance M, Schellenberg G, Mayeux R, Farrer L. Genome-wide association study identifies susceptibility loci associated with the rate of cognitive decline Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.1100 |
0.408 |
|
| 2013 |
Chibnik L, Yu L, Raj T, Xu J, Patsopoulos N, Keenan B, Sherva R, Leurgans S, Blacker D, Wilson R, Reiman E, Huentelman M, Green R, Farrer L, Crane P, et al. Genome-wide association study for cognitive decline Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.1097 |
0.361 |
|
| 2013 |
Nho K, Kim S, Risacher S, Shen L, Sherva R, Green R, Weiner M, Saykin A. P3-013: Imaging genetics of the SPON1
gene variant rs11023139 in Alzheimer's disease Alzheimer's & Dementia. 9: P554-P555. DOI: 10.1016/J.Jalz.2013.05.1082 |
0.406 |
|
| 2013 |
Trittschuh E, Mukherjee S, Thornton T, Fardo D, Waterston L, Crane P, Mez J, Sherva R, Kauwe J, Naj A, Beecham G, Gross A, Saykin A, Green R. P3-003: Genome-wide SNP analysis finds executive-prominent late-onset Alzheimer's disease is highly heritable Alzheimer's & Dementia. 9: P550-P551. DOI: 10.1016/J.Jalz.2013.05.1072 |
0.398 |
|
| 2012 |
Chung SA, Xie G, Roshandel D, Sherva R, Edberg JC, Kravitz M, Dellaripa PF, Hoffman GS, Mahr AD, Seo P, Specks U, Spiera RF, St Clair EW, Stone JH, Plenge RM, et al. Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis. Arthritis and Rheumatism. 64: 3463-71. PMID 22508400 DOI: 10.1002/Art.34496 |
0.435 |
|
| 2011 |
Chen J, Brunzell DH, Jackson K, van der Vaart A, Ma JZ, Payne TJ, Sherva R, Farrer LA, Gejman P, Levinson DF, Holmans P, Aggen SH, Damaj I, Kuo PH, Webb BT, et al. ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. Plos One. 6: e28790. PMID 22205969 DOI: 10.1371/Journal.Pone.0028790 |
0.343 |
|
| 2011 |
Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, et al. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression. Blood. 117: 4935-45. PMID 21385855 DOI: 10.1182/Blood-2010-11-317081 |
0.411 |
|
| 2011 |
Sherva R, Farrer LA. Power and pitfalls of the genome-wide association study approach to identify genes for Alzheimer's disease. Current Psychiatry Reports. 13: 138-46. PMID 21312009 DOI: 10.1007/S11920-011-0184-4 |
0.409 |
|
| 2011 |
Sherva R, Ford CE, Eckfeldt JH, Davis BR, Boerwinkle E, Arnett DK. Pharmacogenetic effect of the stromelysin (MMP3) polymorphism on stroke risk in relation to antihypertensive treatment: the genetics of hypertension associated treatment study. Stroke; a Journal of Cerebral Circulation. 42: 330-5. PMID 21183746 DOI: 10.1161/Strokeaha.110.593798 |
0.317 |
|
| 2011 |
Sherva R, Baldwin CT, Inzelberg R, Vardarajan B, Cupples LA, Lunetta K, Bowirrat A, Naj A, Pericak-Vance M, Friedland RP, Farrer LA. Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data. Journal of Alzheimer's Disease : Jad. 23: 349-59. PMID 21098978 DOI: 10.3233/Jad-2010-100714 |
0.462 |
|
| 2011 |
Love-Gregory L, Sherva R, Schappe T, Qi JS, McCrea J, Klein S, Connelly MA, Abumrad NA. Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profile. Human Molecular Genetics. 20: 193-201. PMID 20935172 DOI: 10.1093/Hmg/Ddq449 |
0.301 |
|
| 2011 |
Sherva R, Tripodis Y, Shulman J, Chibnik L, Crane P, Bennett D, Evans D, Jager PD, Green R. Genetic factors associated with the rate of cognitive decline in Alzheimer's disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.2388 |
0.365 |
|
| 2010 |
Saccone NL, Culverhouse RC, Schwantes-An TH, Cannon DS, Chen X, Cichon S, Giegling I, Han S, Han Y, Keskitalo-Vuokko K, Kong X, Landi MT, Ma JZ, Short SE, Stephens SH, ... ... Sherva R, et al. Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. Plos Genetics. 6. PMID 20700436 DOI: 10.1371/Journal.Pgen.1001053 |
0.374 |
|
| 2010 |
Sherva R, Kranzler HR, Yu Y, Logue MW, Poling J, Arias AJ, Anton RF, Oslin D, Farrer LA, Gelernter J. Variation in nicotinic acetylcholine receptor genes is associated with multiple substance dependence phenotypes. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 35: 1921-31. PMID 20485328 DOI: 10.1038/Npp.2010.64 |
0.426 |
|
| 2010 |
Sherva R, Sripichai O, Abel K, Ma Q, Whitacre J, Angkachatchai V, Makarasara W, Winichagoon P, Svasti S, Fucharoen S, Braun A, Farrer LA. Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study. Bmc Medical Genetics. 11: 51. PMID 20353593 DOI: 10.1186/1471-2350-11-51 |
0.338 |
|
| 2010 |
Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, et al. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Blood. 115: 1815-22. PMID 20018918 DOI: 10.1182/Blood-2009-08-239517 |
0.414 |
|
| 2010 |
Farrell JJ, Sherva RM, Chen Z, Hong-yuan L, Chu BF, Ha SY, Li CK, Lee ACW, Li CK, Yuen HL, So JCC, Ma ES, Chan LC, Chan V, Sebastiani P, et al. A 3-Bp Deletion Between Transcription Factor Binding Motifs In the HBS1L-MYB Intergenic Region on Chromosome 6q23 Is Associated with HbF Expression Blood. 116: 1013-1013. DOI: 10.1182/Blood.V116.21.1013.1013 |
0.381 |
|
| 2009 |
Sherva R, Rice JP, Neuman RJ, Rochberg N, Saccone NL, Bierut LJ. Associations and interactions between SNPs in the alcohol metabolizing genes and alcoholism phenotypes in European Americans. Alcoholism, Clinical and Experimental Research. 33: 848-57. PMID 19298322 DOI: 10.1111/J.1530-0277.2009.00904.X |
0.311 |
|
| 2009 |
Timofeev N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer L, Telen MJ, Ashley-Koch AE, Garrett ME, Chui DH, Baldwin CT, Steinberg MH. Genome-Wide Studies in Sickle Cell Anemia Show Associations Between SNPs in the Olfactory Receptor Gene Cluster and Fetal Hemoglobin Concentration. Blood. 114: 821-821. DOI: 10.1182/Blood.V114.22.821.821 |
0.441 |
|
| 2008 |
Sherva R, Wilhelmsen K, Pomerleau CS, Chasse SA, Rice JP, Snedecor SM, Bierut LJ, Neuman RJ, Pomerleau OF. Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking. Addiction (Abingdon, England). 103: 1544-52. PMID 18783506 DOI: 10.1111/J.1360-0443.2008.02279.X |
0.301 |
|
| 2008 |
Barroso I, Luan J, Wheeler E, Whittaker P, Wasson J, Zeggini E, Weedon MN, Hunt S, Venkatesh R, Frayling TM, Delgado M, Neuman RJ, Zhao J, Sherva R, Glaser B, et al. Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies. Diabetes. 57: 3161-5. PMID 18728231 DOI: 10.2337/Db08-0719 |
0.378 |
|
| 2008 |
Sherva R, Miller MB, Pankow JS, Hunt SC, Boerwinkle E, Mosley TH, Weder AB, Curb JD, Luke A, Morrison AC, Fornage M, Arnett DK. A whole-genome scan for stroke or myocardial infarction in family blood pressure program families. Stroke; a Journal of Cerebral Circulation. 39: 1115-20. PMID 18323513 DOI: 10.1161/Strokeaha.107.490433 |
0.431 |
|
| 2008 |
Love-Gregory L, Sherva R, Sun L, Wasson J, Schappe T, Doria A, Rao DC, Hunt SC, Klein S, Neuman RJ, Permutt MA, Abumrad NA. Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol. Human Molecular Genetics. 17: 1695-704. PMID 18305138 DOI: 10.1093/Hmg/Ddn060 |
0.361 |
|
| 2007 |
Sherva R, Sun L, Biernacka J, Neuman R. No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21. Bmc Proceedings. 1: S42. PMID 18466541 DOI: 10.1186/1753-6561-1-S1-S42 |
0.356 |
|
| 2007 |
Sherva R, Yue P, Schonfeld G, Neuman RJ. Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families. Journal of Lipid Research. 48: 2632-9. PMID 17890784 DOI: 10.1194/Jlr.M700078-Jlr200 |
0.353 |
|
| 2007 |
Sandhu MS, Weedon MN, Fawcett KA, Wasson J, Debenham SL, Daly A, Lango H, Frayling TM, Neumann RJ, Sherva R, Blech I, Pharoah PD, Palmer CN, Kimber C, Tavendale R, et al. Common variants in WFS1 confer risk of type 2 diabetes. Nature Genetics. 39: 951-3. PMID 17603484 DOI: 10.1038/Ng2067 |
0.324 |
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| 2007 |
Sherva R, Miller MB, Lynch AI, Devereux RB, Rao DC, Oberman A, Hopkins PN, Kitzman DW, Atwood LD, Arnett DK. A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study. American Journal of Hypertension. 20: 398-402. PMID 17386346 DOI: 10.1016/J.Amjhyper.2006.10.001 |
0.455 |
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| Show low-probability matches. |