| Year |
Citation |
Score |
| 2020 |
Jaworek T, Ryan KA, Gaynor BJ, McArdle PF, Stine OC, OConnor TD, Lopez H, Aparicio HJ, Gao Y, Lin X, Groves ML, Flaherty ML, Liu S, Yang Q, Wilson J, ... ... Mitchell BD, et al. Exome Array Analysis of Early-Onset Ischemic Stroke. Stroke. STROKEAHA120031357. PMID 32912094 DOI: 10.1161/Strokeaha.120.031357 |
0.376 |
|
| 2020 |
Li X, Li Z, Zhou H, Gaynor SM, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Aslibekyan S, Ballantyne CM, Bielak LF, Blangero J, Boerwinkle E, Bowden DW, ... ... Mitchell BD, et al. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale. Nature Genetics. PMID 32839606 DOI: 10.1038/S41588-020-0676-4 |
0.344 |
|
| 2020 |
Keene KL, Hyacinth HI, Bis JC, Kittner SJ, Mitchell BD, Cheng YC, Pare G, Chong M, O'Donnell M, Meschia JF, Chen WM, Sale MM, Rich SS, Nalls MA, Zonderman AB, et al. Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke. Stroke. STROKEAHA120029123. PMID 32693751 DOI: 10.1161/Strokeaha.120.029123 |
0.36 |
|
| 2020 |
Drake M, Frid P, Hansen BM, Wu O, Giese AK, Schirmer MD, Donahue K, Cloonan L, Irie RE, Bouts MJRJ, McIntosh EC, Mocking SJT, Dalca AV, Sridharan R, Xu H, ... ... Mitchell BD, et al. Diffusion-Weighted Imaging, MR Angiography, and Baseline Data in a Systematic Multicenter Analysis of 3,301 MRI Scans of Ischemic Stroke Patients-Neuroradiological Review Within the MRI-GENIE Study. Frontiers in Neurology. 11: 577. PMID 32670186 DOI: 10.3389/Fneur.2020.00577 |
0.312 |
|
| 2020 |
Giese AK, Schirmer MD, Dalca AV, Sridharan R, Donahue KL, Nardin M, Irie R, McIntosh EC, Mocking SJT, Xu H, Cole JW, Giralt-Steinhauer E, Jimenez-Conde J, Jern C, Kleindorfer DO, ... ... Mitchell BD, et al. White matter hyperintensity burden in acute stroke patients differs by ischemic stroke subtype. Neurology. PMID 32493718 DOI: 10.1212/Wnl.0000000000009728 |
0.304 |
|
| 2020 |
Verma SS, Bergmeijer TO, Gong L, Reny JL, Lewis JP, Mitchell BD, Alexopoulos D, Aradi D, Altman RB, Bliden K, Bradford Y, Campo G, Chang K, Cleator JH, Déry JP, et al. Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC). Clinical Pharmacology and Therapeutics. PMID 32472697 DOI: 10.1002/Cpt.1911 |
0.332 |
|
| 2020 |
Arbeeva L, Yau M, Mitchell BD, Jackson RD, Ryan K, Golightly YM, Hannan MT, Nelson A, Jordan JM, Hochberg MC. Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. Journal of Foot and Ankle Research. 13: 11. PMID 32131869 DOI: 10.1186/S13047-020-0379-1 |
0.377 |
|
| 2020 |
von Berg J, van der Laan SW, McArdle PF, Malik R, Kittner SJ, Mitchell BD, Worrall BB, de Ridder J, Pulit SL. Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. European Journal of Human Genetics : Ejhg. PMID 32047268 DOI: 10.1038/S41431-020-0580-5 |
0.358 |
|
| 2020 |
Kessler MD, Loesch DP, Perry JA, Heard-Costa NL, Taliun D, Cade BE, Wang H, Daya M, Ziniti J, Datta S, Celedón JC, Soto-Quiros ME, Avila L, Weiss ST, Barnes K, ... ... Mitchell BD, et al. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population. Proceedings of the National Academy of Sciences of the United States of America. PMID 31964835 DOI: 10.1073/Pnas.1902766117 |
0.308 |
|
| 2019 |
Raffield LM, Iyengar AK, Wang B, Gaynor SM, Spracklen CN, Zhong X, Kowalski MH, Salimi S, Polfus LM, Benjamin EJ, Bis JC, Bowler R, Cade BE, Choi WJ, Comellas AP, ... ... Mitchell BD, et al. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. American Journal of Human Genetics. PMID 31883642 DOI: 10.1016/J.Ajhg.2019.12.002 |
0.371 |
|
| 2019 |
Sarnowski C, Leong A, Raffield LM, Wu P, de Vries PS, DiCorpo D, Guo X, Xu H, Liu Y, Zheng X, Hu Y, Brody JA, Goodarzi MO, Hidalgo BA, Highland HM, ... ... Mitchell BD, et al. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American Journal of Human Genetics. PMID 31564435 DOI: 10.1016/J.Ajhg.2019.08.010 |
0.38 |
|
| 2019 |
Malik R, Chauhan G, Traylor M, Sargurupremraj M, Okada Y, Mishra A, Rutten-Jacobs L, Giese AK, van der Laan SW, Gretarsdottir S, Anderson CD, Chong M, Adams HHH, Ago T, Almgren P, ... ... Mitchell BD, et al. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nature Genetics. PMID 31160810 DOI: 10.1038/S41588-019-0449-0 |
0.352 |
|
| 2019 |
Hsu YH, Estrada K, Evangelou E, Ackert-Bicknell C, Akesson K, Beck T, Brown SJ, Capellini T, Carbone L, Cauley J, Cheung CL, Cummings SR, Czerwinski S, Demissie S, Econs M, ... ... Mitchell B, et al. Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. e3698. PMID 30888730 DOI: 10.1002/Jbmr.3698 |
0.363 |
|
| 2019 |
Geng X, Irvin MR, Hidalgo B, Aslibekyan S, Srinivasasainagendra V, An P, Frazier-Wood AC, Tiwari HK, Dave T, Ryan K, Ordovas JM, Straka RJ, Feitosa MF, Hopkins PN, Borecki I, ... ... Mitchell BD, et al. An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids. Frontiers in Genetics. 10: 158. PMID 30863429 DOI: 10.3389/Fgene.2019.00158 |
0.382 |
|
| 2019 |
He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang YC, Chen YI, de Vries PS, Fox ER, Franceschini N, Furniss A, ... ... Mitchell BD, et al. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. Human Genetics. PMID 30671673 DOI: 10.1007/S00439-019-01975-0 |
0.375 |
|
| 2019 |
Pfeiffer D, Chen B, Schlicht K, Ginsbach P, Abboud S, Bersano A, Bevan S, Brandt T, Caso V, Debette S, Erhart P, Freitag-Wolf S, Giacalone G, Grau AJ, Hayani E, ... ... Mitchell BD, et al. Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke. Stroke. STROKEAHA118021856. PMID 30661490 DOI: 10.1161/Strokeaha.118.021856 |
0.376 |
|
| 2019 |
Jaworek T, Ryan K, Gaynor B, McArdle P, Stine OC, Aparicio HJ, Gao Y, Lin X, Groves ML, Kittner SJ, Wilson J, Yang Q, Seshadri S, Lui S, Mitchell BD, et al. Abstract WP211: Exome Association Analysis of Small Vessel Young Onset Ischemic Stroke Stroke. 50. DOI: 10.1161/Str.50.Suppl_1.Wp211 |
0.313 |
|
| 2019 |
Simpkins AN, McDonough CW, McClure LA, Mitchell BD, Shuldiner AR, Benavente OR, Johnson JA. Abstract 37: Secondary Stroke Prevention With Aspirin and Clopidogrel in
CYP2C19
*17 Carriers Increases Risk of Major Non-CNS Bleeding Stroke. 50. DOI: 10.1161/Str.50.Suppl_1.37 |
0.313 |
|
| 2018 |
Chen H, Huffman JE, Brody JA, Wang C, Lee S, Li Z, Gogarten SM, Sofer T, Bielak LF, Bis JC, Blangero J, Bowler RP, Cade BE, Cho MH, Correa A, ... ... Mitchell BD, et al. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30639324 DOI: 10.1016/J.Ajhg.2018.12.012 |
0.314 |
|
| 2018 |
Pulit SL, Weng LC, McArdle PF, Trinquart L, Choi SH, Mitchell BD, Rosand J, de Bakker PIW, Benjamin EJ, Ellinor PT, Kittner SJ, Lubitz SA, Anderson CD. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. Neurology. Genetics. 4: e293. PMID 30584597 DOI: 10.1212/Nxg.0000000000000293 |
0.325 |
|
| 2018 |
Mola-Caminal M, Carrera C, Soriano-Tárraga C, Giralt Steinhauer E, Diaz-Navarro RM, Tur S, Jiménez C, Medina-Dols A, Cullell N, Torres-Aguila NP, Muiño E, Rodri Guez-Campello A, Ois A, Cuadrado-Godia E, Vivanco-Hidalgo RM, ... ... Mitchell BD, et al. PATJ Low Frequency Variants Are Associated with Worse Ischemic Stroke Functional Outcome: A Genome-Wide Meta-Analysis. Circulation Research. PMID 30582445 DOI: 10.1161/Circresaha.118.313533 |
0.335 |
|
| 2018 |
Kochunov P, Donohue B, Mitchell BD, Ganjgahi H, Adhikari B, Ryan M, Medland SE, Jahanshad N, Thompson PM, Blangero J, Fieremans E, Novikov DS, Marcus D, Van Essen DC, Glahn DC, et al. Genomic kinship construction to enhance genetic analyses in the human connectome project data. Human Brain Mapping. PMID 30496643 DOI: 10.1002/Hbm.24479 |
0.319 |
|
| 2018 |
Cole JW, Xu H, Ryan K, Jaworek T, Dueker N, McArdle P, Gaynor B, Cheng YC, O'Connell J, Bevan S, Malik R, Ahmed NU, Amouyel P, Anjum S, Bis JC, ... ... Mitchell BD, et al. Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke. Plos One. 13: e0206554. PMID 30383853 DOI: 10.1371/Journal.Pone.0206554 |
0.711 |
|
| 2018 |
Suri P, Palmer MR, Tsepilov YA, Freidin MB, Boer CG, Yau MS, Evans DS, Gelemanovic A, Bartz TM, Nethander M, Arbeeva L, Karssen L, Neogi T, Campbell A, Mellstrom D, ... ... Mitchell BD, et al. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain. Plos Genetics. 14: e1007601. PMID 30261039 DOI: 10.1371/Journal.Pgen.1007601 |
0.365 |
|
| 2018 |
El Rouby N, McDonough CW, Gong Y, McClure LA, Mitchell BD, Horenstein RB, Talbert RL, Crawford DC, Gitzendanner MA, Takahashi A, Tanaka T, Kubo M, Pepine CJ, Cooper-DeHoff RM, et al. Genome-wide association analysis of common genetic variants of resistant hypertension. The Pharmacogenomics Journal. PMID 30237584 DOI: 10.1038/S41397-018-0049-X |
0.405 |
|
| 2018 |
Natarajan P, Peloso GM, Zekavat SM, Montasser M, Ganna A, Chaffin M, Khera AV, Zhou W, Bloom JM, Engreitz JM, Ernst J, O'Connell JR, Ruotsalainen SE, Alver M, Manichaikul A, ... ... Mitchell B, et al. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals. Nature Communications. 9: 3391. PMID 30140000 DOI: 10.1038/S41467-018-05747-8 |
0.337 |
|
| 2018 |
van Setten J, Brody JA, Jamshidi Y, Swenson BR, Butler AM, Campbell H, Del Greco FM, Evans DS, Gibson Q, Gudbjartsson DF, Kerr KF, Krijthe BP, Lyytikäinen LP, Müller C, Müller-Nurasyid M, ... ... Mitchell BD, et al. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nature Communications. 9: 2904. PMID 30046033 DOI: 10.1038/S41467-018-04766-9 |
0.332 |
|
| 2018 |
Zekavat SM, Ruotsalainen S, Handsaker RE, Alver M, Bloom J, Poterba T, Seed C, Ernst J, Chaffin M, Engreitz J, Peloso GM, Manichaikul A, Yang C, Ryan KA, Fu M, ... ... Mitchell BD, et al. Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. Nature Communications. 9: 2606. PMID 29973585 DOI: 10.1038/S41467-018-04668-W |
0.358 |
|
| 2018 |
Bergmeijer TO, Reny JL, Pakyz RE, Gong L, Lewis JP, Kim EY, Aradi D, Fernandez-Cadenas I, Horenstein RB, Lee MTM, Whaley RM, Montaner J, Gensini GF, Cleator JH, Chang K, ... ... Mitchell BD, et al. Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical end points-Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC). American Heart Journal. 198: 152-159. PMID 29653637 DOI: 10.1016/J.Ahj.2017.12.010 |
0.349 |
|
| 2018 |
Montasser ME, O'Hare EA, Wang X, Howard AD, McFarland R, Perry JA, Ryan KA, Rice K, Jaquish CE, Shuldiner AR, Miller M, Mitchell BD, Zaghloul NA, Chang YC. AnPseudogene on Chromosome 5q is Associated with LDL-C Levels. Circulation. PMID 29593015 DOI: 10.1161/Circulationaha.118.034016 |
0.339 |
|
| 2018 |
Xu H, Dorn Ii GW, Shetty A, Parihar A, Dave T, Robinson SW, Gottlieb SS, Donahue MP, Tomaselli GF, Kraus WE, Mitchell BD, Liggett SB. A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans. Journal of Personalized Medicine. 8. PMID 29495422 DOI: 10.3390/Jpm8010011 |
0.352 |
|
| 2018 |
Geng X, Irvin MR, Hidalgo B, Aslibekyan S, Srinivasasainagendra V, An P, Frazier-Wood A, Tiwari HK, Dave T, Ryan K, Ordovas JM, Straka RJ, Feitosa MF, Hopkins PN, Borecki I, ... ... Mitchell BD, et al. An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort. Journal of Lipid Research. PMID 29463568 DOI: 10.1194/Jlr.P080333 |
0.345 |
|
| 2018 |
Wassertheil-Smoller S, Qi Q, Dave T, Mitchell BD, Jackson RD, Liu S, Park K, Salinas J, Dunn EC, Leira EC, Xu H, Ryan K, Smoller JW. Polygenic Risk for Depression Increases Risk of Ischemic Stroke: From the Stroke Genetics Network Study. Stroke. PMID 29438084 DOI: 10.1161/Strokeaha.117.018857 |
0.326 |
|
| 2018 |
Cole JW, Jaworek T, Ryan K, Gaynor B, McArdle P, Stine OC, Aparicio HJ, Gao Y, Lin X, Grove ML, Kittner SJ, Wilson JG, Yang Q, Seshadri S, Lui S, ... Mitchell BD, et al. Abstract WP160: Exome Array Analysis of Early-Onset Ischemic Stroke Stroke. 49. DOI: 10.1161/Str.49.Suppl_1.Wp160 |
0.341 |
|
| 2018 |
Giese A, Xu H, Schirmer MD, Donahue KL, Dalca AV, Gaynor BJ, Cole JW, McArdle PF, Broderick JP, Jimenez-Conde J, Jern C, Kissela BM, Kleindorfer DO, Lemmens R, Lindgren A, ... ... Mitchell BD, et al. Abstract WMP56: Genetics of Acute Ischemic Lesion Volume: the MRI-Genetics Interface Exploration (MRI-GENIE) Study Stroke. 49. DOI: 10.1161/Str.49.Suppl_1.Wmp56 |
0.355 |
|
| 2017 |
Wadhawan A, Dagdag A, Duffy A, Daue ML, Ryan KA, Brenner LA, Stiller JW, Pollin TI, Groer MW, Huang X, Lowry CA, Mitchell BD, Postolache TT. Positive association between IgG serointensity and current dysphoria/hopelessness scores in the Old Order Amish: a preliminary study. Pteridines. 28: 185-194. PMID 29657363 DOI: 10.1515/Pterid-2017-0019 |
0.311 |
|
| 2017 |
Willems SM, Wright DJ, Day FR, Trajanoska K, Joshi PK, Morris JA, Matteini AM, Garton FC, Grarup N, Oskolkov N, Thalamuthu A, Mangino M, Liu J, Demirkan A, Lek M, ... ... Mitchell BD, et al. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Nature Communications. 8: 16015. PMID 29313844 DOI: 10.1038/Ncomms16015 |
0.327 |
|
| 2017 |
Oates CP, Koenig D, Rhyne J, Bogush N, O'Connell J, Mitchell BD, Miller M. Novel polymorphisms associated with hyperalphalipoproteinemia and apparent cardioprotection. Journal of Clinical Lipidology. PMID 29198934 DOI: 10.1016/J.Jacl.2017.10.021 |
0.329 |
|
| 2017 |
Phuah CL, Dave T, Malik R, Raffeld MR, Ayres AM, Goldstein JN, Viswanathan A, Greenberg SM, Jagiella JM, Hansen BM, Norrving B, Jimenez-Conde J, Roquer J, Pichler A, Enzinger C, ... ... Mitchell BD, et al. Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke. Brain : a Journal of Neurology. 140: 2663-2672. PMID 28969386 DOI: 10.1093/Brain/Awx220 |
0.399 |
|
| 2017 |
Rannikmäe K, Sivakumaran V, Millar H, Malik R, Anderson CD, Chong M, Dave T, Falcone GJ, Fernandez-Cadenas I, Jimenez-Conde J, Lindgren A, Montaner J, O'Donnell M, Paré G, Radmanesh F, ... ... Mitchell BD, et al. COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology. PMID 28954878 DOI: 10.1212/Wnl.0000000000004560 |
0.354 |
|
| 2017 |
Giese AK, Schirmer MD, Donahue KL, Cloonan L, Irie R, Winzeck S, Bouts MJRJ, McIntosh EC, Mocking SJ, Dalca AV, Sridharan R, Xu H, Frid P, Giralt-Steinhauer E, Holmegaard L, ... ... Mitchell BD, et al. Design and rationale for examining neuroimaging genetics in ischemic stroke: The MRI-GENIE study. Neurology. Genetics. 3: e180. PMID 28852707 DOI: 10.1212/Nxg.0000000000000180 |
0.314 |
|
| 2017 |
Zillikens MC, Demissie S, Hsu YH, Yerges-Armstrong LM, Chou WC, Stolk L, Livshits G, Broer L, Johnson T, Koller DL, Kutalik Z, Luan J, Malkin I, Ried JS, Smith AV, ... ... Mitchell BD, et al. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nature Communications. 8: 80. PMID 28724990 DOI: 10.1038/S41467-017-00031-7 |
0.314 |
|
| 2017 |
Mitchell BD. Holy Smokes-An Interaction! Circulation. 135: 2354-2356. PMID 28606948 DOI: 10.1161/Circulationaha.117.028476 |
0.318 |
|
| 2017 |
Xu H, Ryan KA, Jaworek TJ, Southam L, Reid JG, Overton JD, Baras A, Puurunen MK, Zeggini E, Taylor SI, Shuldiner AR, Mitchell BD. Familial Hypercholesterolemia and Type 2 Diabetes in the Old Order Amish. Diabetes. PMID 28428224 DOI: 10.2337/Db17-0173 |
0.377 |
|
| 2017 |
Magvanjav O, McDonough CW, Gong Y, McClure LA, Talbert RL, Horenstein RB, Shuldiner AR, Benavente OR, Mitchell BD, Johnson JA. Pharmacogenetic Associations of β1-Adrenergic Receptor Polymorphisms With Cardiovascular Outcomes in the SPS3 Trial (Secondary Prevention of Small Subcortical Strokes). Stroke. PMID 28351962 DOI: 10.1161/Strokeaha.116.015936 |
0.326 |
|
| 2017 |
Xu H, Mitchell BD, Peprah E, Kittner SJ, Cole JW. The Importance of Conducting Stroke Genomics Research in African Ancestry Populations. Global Heart. PMID 28336388 DOI: 10.1016/J.Gheart.2017.01.004 |
0.312 |
|
| 2017 |
Backman JD, O'Connell JR, Tanner K, Peer CJ, Figg WD, Spencer SD, Mitchell BD, Shuldiner AR, Yerges-Armstrong LM, Horenstein RB, Lewis JP. Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response. Pharmacogenetics and Genomics. PMID 28207573 DOI: 10.1097/Fpc.0000000000000272 |
0.379 |
|
| 2016 |
D'Adamo CR, Dawson VJ, Ryan KA, Yerges-Armstrong LM, Semba RD, Steinle NI, Mitchell BD, Shuldiner AR, McArdle PF. The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Journal of Nutrigenetics and Nutrigenomics. 9: 254-264. PMID 28002826 DOI: 10.1159/000452890 |
0.316 |
|
| 2016 |
Traylor M, Malik R, Nalls MA, Cotlarciuc I, Radmanesh F, Thorleifsson G, Hanscombe KB, Langefeld C, Saleheen D, Rost NS, Yet I, Spector TD, Bell JT, Hannon E, Mill J, ... ... Mitchell BD, et al. Genetic Variation at 16q24.2 is associated with small vessel stroke. Annals of Neurology. PMID 27997041 DOI: 10.1002/Ana.24840 |
0.383 |
|
| 2016 |
Robinson-Cohen C, Lutsey PL, Kleber ME, Nielson CM, Mitchell BD, Bis JC, Eny KM, Portas L, Eriksson J, Lorentzon M, Koller DL, Milaneschi Y, Teumer A, Pilz S, Nethander M, et al. Genetic Variants Associated with Circulating Parathyroid Hormone. Journal of the American Society of Nephrology : Jasn. PMID 27927781 DOI: 10.1681/Asn.2016010069 |
0.358 |
|
| 2016 |
Chu AY, Deng X, Fisher VA, Drong A, Zhang Y, Feitosa MF, Liu CT, Weeks O, Choh AC, Duan Q, Dyer TD, Eicher JD, Guo X, Heard-Costa NL, Kacprowski T, ... ... Mitchell BD, et al. Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Nature Genetics. PMID 27918534 DOI: 10.1038/Ng.3738 |
0.573 |
|
| 2016 |
Natarajan P, Bis JC, Bielak LF, Cox AJ, Dörr M, Feitosa MF, Franceschini N, Guo X, Hwang SJ, Isaacs A, Jhun MA, Kavousi M, Li-Gao R, Lyytikäinen LP, Marioni RE, ... ... Mitchell BD, et al. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. Circulation. Cardiovascular Genetics. PMID 27872105 DOI: 10.1161/Circgenetics.116.001572 |
0.353 |
|
| 2016 |
Castaño-Betancourt MC, Evans DS, Ramos YF, Boer CG, Metrustry S, Liu Y, den Hollander W, van Rooij J, Kraus VB, Yau MS, Mitchell BD, Muir K, Hofman A, Doherty M, Doherty S, et al. Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis. Plos Genetics. 12: e1006260. PMID 27701424 DOI: 10.1371/Journal.Pgen.1006260 |
0.383 |
|
| 2016 |
Yau MS, Yerges-Armstrong LM, Liu Y, Lewis CE, Duggan DJ, Renner JB, Torner J, Felson DT, McCulloch CE, Kwoh CK, Nevitt MC, Hochberg MC, Mitchell BD, Jordan JM, Jackson RD. Genome-wide Association Study of Radiographic Knee Osteoarthritis in North American Caucasians. Arthritis & Rheumatology (Hoboken, N.J.). PMID 27696742 DOI: 10.1002/Art.39932 |
0.329 |
|
| 2016 |
Winkler TW, Justice AE, Graff M, Barata L, Feitosa MF, Chu S, Czajkowski J, Esko T, Fall T, Kilpeläinen TO, Lu Y, Mägi R, Mihailov E, Pers TH, Rüeger S, ... ... Mitchell BD, et al. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Plos Genetics. 12: e1006166. PMID 27355579 DOI: 10.1371/Journal.Pgen.1006166 |
0.673 |
|
| 2016 |
Malik R, Traylor M, Pulit SL, Bevan S, Hopewell JC, Holliday EG, Zhao W, Abrantes P, Amouyel P, Attia JR, Battey TW, Berger K, Boncoraglio GB, Chauhan G, Cheng YC, ... ... Mitchell BD, et al. Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology. PMID 26935894 DOI: 10.1212/Wnl.0000000000002528 |
0.336 |
|
| 2016 |
Yerges-Armstrong LM, Chai S, O'Connell JR, Curran JE, Blangero J, Mitchell BD, Shuldiner AR, Damcott CM. Gene Expression Differences Between Offspring of Long-Lived Individuals and Controls in Candidate Longevity Regions: Evidence for PAPSS2 as a Longevity Gene. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 26896383 DOI: 10.1093/Gerona/Glv212 |
0.34 |
|
| 2016 |
D'Adamo CR, D'Urso A, Ryan KA, Yerges-Armstrong LM, Semba RD, Steinle NI, Mitchell BD, Shuldiner AR, McArdle PF. A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations. Nutrients. 8. PMID 26861389 DOI: 10.3390/Nu8020082 |
0.343 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, ... ... Mitchell BD, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.325 |
|
| 2016 |
Cheng YC, Stanne TM, Giese AK, Ho WK, Traylor M, Amouyel P, Holliday EG, Malik R, Xu H, Kittner SJ, Cole JW, O'Connell JR, Danesh J, Rasheed A, Zhao W, ... ... Mitchell BD, et al. Genome-Wide Association Analysis of Young Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Stroke; a Journal of Cerebral Circulation. PMID 26732560 DOI: 10.1161/Strokeaha.115.011328 |
0.383 |
|
| 2016 |
Rosand J, Mitchell BD, Ay H, de Bakker PIW, Gwinn K, Kittner SJ, Lindgren A, Meschia JF, Pulit SL, Sudlow CLM, Thijs V, Woo D, Worrall BB, Arnett DK, Benavente O, et al. Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study The Lancet Neurology. 15: 174-184. DOI: 10.1016/S1474-4422(15)00338-5 |
0.373 |
|
| 2015 |
Teumer A, Tin A, Sorice R, Gorski M, Yeo NC, Chu AY, Li M, Li Y, Mijatovic V, Ko YA, Taliun D, Luciani A, Chen MH, Yang Q, Foster MC, ... ... Mitchell BD, et al. Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes. Diabetes. PMID 26631737 DOI: 10.2337/Db15-1313 |
0.378 |
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| 2015 |
Winkler TW, Justice AE, Graff M, Barata L, Feitosa MF, Chu S, Czajkowski J, Esko T, Fall T, Kilpeläinen TO, Lu Y, Mägi R, Mihailov E, Pers TH, Rüeger S, ... ... Mitchell BD, et al. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Plos Genetics. 11: e1005378. PMID 26426971 DOI: 10.1371/Journal.Pgen.1005378 |
0.703 |
|
| 2015 |
Fisch AS, Yerges-Armstrong LM, Backman JD, Wang H, Donnelly P, Ryan KA, Parihar A, Pavlovich MA, Mitchell BD, O'Connell JR, Herzog W, Harman CR, Wren JD, Lewis JP. Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction. Plos One. 10: e0138795. PMID 26406321 DOI: 10.1371/Journal.Pone.0138795 |
0.303 |
|
| 2015 |
Bluher A, Devan WJ, Holliday EG, Nalls M, Parolo S, Bione S, Giese AK, Boncoraglio GB, Maguire JM, Müller-Nurasyid M, Gieger C, Meschia JF, Rosand J, Rolfs A, Kittner SJ, ... Mitchell BD, et al. Heritability of young- and old-onset ischaemic stroke. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. PMID 26333310 DOI: 10.1111/Ene.12827 |
0.361 |
|
| 2015 |
Carty CL, Keene KL, Cheng YC, Meschia JF, Chen WM, Nalls M, Bis JC, Kittner SJ, Rich SS, Tajuddin S, Zonderman AB, Evans MK, Langefeld CD, Gottesman R, Mosley TH, ... ... Mitchell BD, et al. Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans. Stroke; a Journal of Cerebral Circulation. PMID 26089329 DOI: 10.1161/Strokeaha.115.009044 |
0.373 |
|
| 2015 |
McDonough CW, McClure LA, Mitchell BD, Gong Y, Horenstein RB, Lewis JP, Field TS, Talbert RL, Benavente OR, Johnson JA, Shuldiner AR. CYP2C19 metabolizer status and clopidogrel efficacy in the Secondary Prevention of Small Subcortical Strokes (SPS3) study. Journal of the American Heart Association. 4: e001652. PMID 26019129 DOI: 10.1161/Jaha.114.001652 |
0.342 |
|
| 2015 |
Mitchell AB, Cole JW, McArdle PF, Cheng YC, Ryan KA, Sparks MJ, Mitchell BD, Kittner SJ. Obesity increases risk of ischemic stroke in young adults. Stroke; a Journal of Cerebral Circulation. 46: 1690-2. PMID 25944320 DOI: 10.1161/Strokeaha.115.008940 |
0.315 |
|
| 2015 |
Malik R, Freilinger T, Winsvold BS, Anttila V, Vander Heiden J, Traylor M, de Vries B, Holliday EG, Terwindt GM, Sturm J, Bis JC, Hopewell JC, Ferrari MD, Rannikmae K, Wessman M, ... ... Mitchell BD, et al. Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants. Neurology. 84: 2132-45. PMID 25934857 DOI: 10.1212/Wnl.0000000000001606 |
0.361 |
|
| 2015 |
Kochunov P, Jahanshad N, Marcus D, Winkler A, Sprooten E, Nichols TE, Wright SN, Hong LE, Patel B, Behrens T, Jbabdi S, Andersson J, Lenglet C, Yacoub E, Moeller S, ... ... Mitchell B, et al. Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data. Neuroimage. 111: 300-11. PMID 25747917 DOI: 10.1016/J.Neuroimage.2015.02.050 |
0.317 |
|
| 2015 |
Rannikmäe K, Davies G, Thomson PA, Bevan S, Devan WJ, Falcone GJ, Traylor M, Anderson CD, Battey TW, Radmanesh F, Deka R, Woo JG, Martin LJ, Jimenez-Conde J, Selim M, ... ... Mitchell BD, et al. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology. 84: 918-26. PMID 25653287 DOI: 10.1212/Wnl.0000000000001309 |
0.316 |
|
| 2015 |
Holliday EG, Traylor M, Malik R, Bevan S, Falcone G, Hopewell JC, Cheng YC, Cotlarciuc I, Bis JC, Boerwinkle E, Boncoraglio GB, Clarke R, Cole JW, Fornage M, Furie KL, ... ... Mitchell BD, et al. Genetic overlap between diagnostic subtypes of ischemic stroke. Stroke; a Journal of Cerebral Circulation. 46: 615-9. PMID 25613305 DOI: 10.1161/Strokeaha.114.007930 |
0.35 |
|
| 2015 |
Lu W, Cheng YC, Chen K, Wang H, Gerhard GS, Still CD, Chu X, Yang R, Parihar A, O'Connell JR, Pollin TI, Angles-Cano E, Quon MJ, Mitchell BD, Shuldiner AR, et al. Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels. Human Molecular Genetics. 24: 2390-400. PMID 25575512 DOI: 10.1093/Hmg/Ddu731 |
0.358 |
|
| 2015 |
Byrne EM, Raheja UK, Stephens SH, Heath AC, Madden PA, Vaswani D, Nijjar GV, Ryan KA, Youssufi H, Gehrman PR, Shuldiner AR, Martin NG, Montgomery GW, Wray NR, ... ... Mitchell BD, et al. Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder. The Journal of Clinical Psychiatry. 76: 128-34. PMID 25562672 DOI: 10.4088/Jcp.14M08981 |
0.301 |
|
| 2015 |
Gorski M, Tin A, Garnaas M, McMahon GM, Chu AY, Tayo BO, Pattaro C, Teumer A, Chasman DI, Chalmers J, Hamet P, Tremblay J, Woodward M, Aspelund T, Eiriksdottir G, ... ... Mitchell BD, et al. Genome-wide association study of kidney function decline in individuals of European descent. Kidney International. 87: 1017-29. PMID 25493955 DOI: 10.1038/Ki.2014.361 |
0.338 |
|
| 2014 |
Holliday EG, Traylor M, Malik R, Bevan S, Maguire J, Koblar SA, Sturm J, Hankey GJ, Oldmeadow C, McEvoy M, Sudlow C, Rothwell PM, Coresh J, Hamet P, Tremblay J, ... ... Mitchell BD, et al. Polygenic overlap between kidney function and large artery atherosclerotic stroke. Stroke; a Journal of Cerebral Circulation. 45: 3508-13. PMID 25352485 DOI: 10.1161/Strokeaha.114.006609 |
0.349 |
|
| 2014 |
Parihar A, Wood GC, Chu X, Jin Q, Argyropoulos G, Still CD, Shuldiner AR, Mitchell BD, Gerhard GS. Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip. Frontiers in Genetics. 5: 222. PMID 25147553 DOI: 10.3389/Fgene.2014.00222 |
0.361 |
|
| 2014 |
Traylor M, Mäkelä KM, Kilarski LL, Holliday EG, Devan WJ, Nalls MA, Wiggins KL, Zhao W, Cheng YC, Achterberg S, Malik R, Sudlow C, Bevan S, Raitoharju E, ... ... Mitchell BD, et al. A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. Plos Genetics. 10: e1004469. PMID 25078452 DOI: 10.1371/Journal.Pgen.1004469 |
0.405 |
|
| 2014 |
Kilarski LL, Achterberg S, Devan WJ, Traylor M, Malik R, Lindgren A, Pare G, Sharma P, Slowik A, Thijs V, Walters M, Worrall BB, Sale MM, Algra A, Kappelle LJ, ... ... Mitchell BD, et al. Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. Neurology. 83: 678-85. PMID 25031287 DOI: 10.1212/Wnl.0000000000000707 |
0.351 |
|
| 2014 |
Cheng YC, Cole JW, Kittner SJ, Mitchell BD. Genetics of ischemic stroke in young adults. Circulation. Cardiovascular Genetics. 7: 383-92. PMID 24951665 DOI: 10.1161/Circgenetics.113.000390 |
0.382 |
|
| 2014 |
Cotlarciuc I, Malik R, Holliday EG, Ahmadi KR, Paré G, Psaty BM, Fornage M, Hasan N, Rinne PE, Ikram MA, Markus HS, Rosand J, Mitchell BD, Kittner SJ, Meschia JF, et al. Effect of genetic variants associated with plasma homocysteine levels on stroke risk. Stroke; a Journal of Cerebral Circulation. 45: 1920-4. PMID 24846872 DOI: 10.1161/Strokeaha.114.005208 |
0.382 |
|
| 2014 |
Mitchell BD, Fornage M, McArdle PF, Cheng YC, Pulit SL, Wong Q, Dave T, Williams SR, Corriveau R, Gwinn K, Doheny K, Laurie CC, Rich SS, de Bakker PI. Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN). Frontiers in Genetics. 5: 95. PMID 24808905 DOI: 10.3389/Fgene.2014.00095 |
0.372 |
|
| 2014 |
Maruthur NM, Mitchell BD. Zinc-rs13266634 and the arrival of diabetes pharmacogenetics: the "zinc mystique". Diabetes. 63: 1463-4. PMID 24757200 DOI: 10.2337/Db14-0151 |
0.372 |
|
| 2014 |
Kochunov P, Jahanshad N, Sprooten E, Nichols TE, Mandl RC, Almasy L, Booth T, Brouwer RM, Curran JE, de Zubicaray GI, Dimitrova R, Duggirala R, Fox PT, Hong LE, Landman BA, ... ... Mitchell BD, et al. Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling. Neuroimage. 95: 136-50. PMID 24657781 DOI: 10.1016/J.Neuroimage.2014.03.033 |
0.307 |
|
| 2014 |
Jiang B, Ryan KA, Hamedani A, Cheng Y, Sparks MJ, Koontz D, Bean CJ, Gallagher M, Hooper WC, McArdle PF, O'Connell JR, Stine OC, Wozniak MA, Stern BJ, Mitchell BD, et al. Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis. Stroke; a Journal of Cerebral Circulation. 45: 961-7. PMID 24619398 DOI: 10.1161/Strokeaha.113.004063 |
0.331 |
|
| 2014 |
Liu X, Post WS, McLenithan J, Terrin M, Magder L, Zeb I, Budoff M, Mitchell BD. Determinants of intrathoracic adipose tissue volume and associations with cardiovascular disease risk factors in Amish. Nutrition, Metabolism, and Cardiovascular Diseases : Nmcd. 24: 286-93. PMID 24477004 DOI: 10.1016/J.Numecd.2013.09.015 |
0.516 |
|
| 2014 |
Ryan KA, Cole JW, Saslow K, Mitchell BD, McArdle PF, Sparks MJ, Cheng YC, Kittner SJ. Prevention opportunities for oral contraceptive-associated ischemic stroke. Stroke; a Journal of Cerebral Circulation. 45: 893-5. PMID 24448988 DOI: 10.1161/Strokeaha.113.004023 |
0.318 |
|
| 2014 |
Malik R, Bevan S, Nalls MA, Holliday EG, Devan WJ, Cheng YC, Ibrahim-Verbaas CA, Verhaaren BF, Bis JC, Joon AY, de Stefano AL, Fornage M, Psaty BM, Ikram MA, Launer LJ, ... ... Mitchell BD, et al. Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies. Stroke; a Journal of Cerebral Circulation. 45: 394-402. PMID 24436234 DOI: 10.1161/Strokeaha.113.002938 |
0.381 |
|
| 2014 |
Yoneyama S, Guo Y, Lanktree MB, Barnes MR, Elbers CC, Karczewski KJ, Padmanabhan S, Bauer F, Baumert J, Beitelshees A, Berenson GS, Boer JM, Burke G, Cade B, Chen W, ... ... Mitchell BD, et al. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Human Molecular Genetics. 23: 2498-510. PMID 24345515 DOI: 10.1093/Hmg/Ddt626 |
0.364 |
|
| 2014 |
Yerges-Armstrong LM, Yau MS, Liu Y, Krishnan S, Renner JB, Eaton CB, Kwoh CK, Nevitt MC, Duggan DJ, Mitchell BD, Jordan JM, Hochberg MC, Jackson RD. Association analysis of BMD-associated SNPs with knee osteoarthritis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 1373-9. PMID 24339167 DOI: 10.1002/Jbmr.2160 |
0.376 |
|
| 2014 |
Dichgans M, Malik R, König IR, Rosand J, Clarke R, Gretarsdottir S, Thorleifsson G, Mitchell BD, Assimes TL, Levi C, O'Donnell CJ, Fornage M, Thorsteinsdottir U, Psaty BM, Hengstenberg C, et al. Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Stroke; a Journal of Cerebral Circulation. 45: 24-36. PMID 24262325 DOI: 10.1161/Strokeaha.113.002707 |
0.379 |
|
| 2014 |
Wang G, Padmanabhan S, Miyamoto-Mikami E, Fuku N, Tanaka M, Miyachi M, Murakami H, Cheng Y, Mitchell BD, Austin KG, Pitsiladis YP. GWAS of Elite Jamaican, African American and Japanese Sprint Athletes Medicine & Science in Sports & Exercise. 46: 596. DOI: 10.1249/01.Mss.0000451226.19286.0D |
0.354 |
|
| 2014 |
Yerges-Armstrong L, Nevitt M, Yau M, Lane N, Duggan D, Jungmann P, Mitchell B, Jackson R, Hochberg M. Genetic association analysis of radiographic hip osteoarthritis with established loci for bone mineral density: data from the osteoarthritis initiative Osteoarthritis and Cartilage. 22: S234. DOI: 10.1016/J.Joca.2014.02.451 |
0.361 |
|
| 2014 |
WF, Carter AM, Hysi PG, Surdulescu G, Hodgkiss D, Soranzo N, Traylor M, Bevan S, Dichgans M, RP, Sudlow C, Farrall M, Silander K, Kaunisto M, Wagner P, ... ... Mitchell BD, et al. Erratum: Ischemic stroke is associated with the ABO locus: The EuroCLOT study (Annals of Neurology (2013) 73 (16-31)) Annals of Neurology. 75: 166-167. DOI: 10.1002/Ana.24105 |
0.325 |
|
| 2013 |
Stephens SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ, Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han Y, ... ... Mitchell BD, et al. Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology. 37: 846-59. PMID 24186853 DOI: 10.1002/Gepi.21760 |
0.697 |
|
| 2013 |
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, ... ... Mitchell BD, et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics. 45: 1274-83. PMID 24097068 DOI: 10.1038/Ng.2797 |
0.366 |
|
| 2013 |
Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, ... ... Mitchell BD, et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics. 45: 1345-52. PMID 24097064 DOI: 10.1038/Ng.2795 |
0.331 |
|
| 2013 |
Parsa A, Fuchsberger C, Köttgen A, O'Seaghdha CM, Pattaro C, de Andrade M, Chasman DI, Teumer A, Endlich K, Olden M, Chen MH, Tin A, Kim YJ, Taliun D, Li M, ... ... Mitchell BD, et al. Common variants in Mendelian kidney disease genes and their association with renal function. Journal of the American Society of Nephrology : Jasn. 24: 2105-17. PMID 24029420 DOI: 10.1681/Asn.2012100983 |
0.364 |
|
| 2013 |
Meschia JF, Arnett DK, Ay H, Brown RD, Benavente OR, Cole JW, de Bakker PI, Dichgans M, Doheny KF, Fornage M, Grewal RP, Gwinn K, Jern C, Conde JJ, Johnson JA, ... ... Mitchell BD, et al. Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. Stroke; a Journal of Cerebral Circulation. 44: 2694-702. PMID 24021684 DOI: 10.1161/Strokeaha.113.001857 |
0.352 |
|
| 2013 |
Yadav S, Cotlarciuc I, Munroe PB, Khan MS, Nalls MA, Bevan S, Cheng YC, Chen WM, Malik R, McCarthy NS, Holliday EG, Speed D, Hasan N, Pucek M, Rinne PE, ... ... Mitchell BD, et al. Genome-wide analysis of blood pressure variability and ischemic stroke. Stroke; a Journal of Cerebral Circulation. 44: 2703-9. PMID 23929743 DOI: 10.1161/Strokeaha.113.002186 |
0.401 |
|
| 2013 |
Adib-Samii P, Rost N, Traylor M, Devan W, Biffi A, Lanfranconi S, Fitzpatrick K, Bevan S, Kanakis A, Valant V, Gschwendtner A, Malik R, Richie A, Gamble D, Segal H, ... ... Mitchell BD, et al. 17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status. Stroke; a Journal of Cerebral Circulation. 44: 1609-15. PMID 23674528 DOI: 10.1161/Strokeaha.113.679936 |
0.331 |
|
| 2013 |
Jahanshad N, Kochunov PV, Sprooten E, Mandl RC, Nichols TE, Almasy L, Blangero J, Brouwer RM, Curran JE, de Zubicaray GI, Duggirala R, Fox PT, Hong LE, Landman BA, Martin NG, ... ... Mitchell BD, et al. Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA-DTI working group. Neuroimage. 81: 455-69. PMID 23629049 DOI: 10.1016/J.Neuroimage.2013.04.061 |
0.305 |
|
| 2013 |
Harriott AM, Dueker N, Cheng YC, Ryan KA, O'Connell JR, Stine OC, McArdle PF, Wozniak MA, Stern BJ, Mitchell BD, Kittner SJ, Cole JW. Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study. Springerplus. 2: 46. PMID 23459313 DOI: 10.1186/2193-1801-2-46 |
0.738 |
|
| 2013 |
Lewis JP, Ryan K, O'Connell JR, Horenstein RB, Damcott CM, Gibson Q, Pollin TI, Mitchell BD, Beitelshees AL, Pakzy R, Tanner K, Parsa A, Tantry US, Bliden KP, Post WS, et al. Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes. Circulation. Cardiovascular Genetics. 6: 184-92. PMID 23392654 DOI: 10.1161/Circgenetics.111.964627 |
0.361 |
|
| 2013 |
Williams FM, Carter AM, Hysi PG, Surdulescu G, Hodgkiss D, Soranzo N, Traylor M, Bevan S, Dichgans M, Rothwell PM, Sudlow C, Farrall M, Silander K, Kaunisto M, Wagner P, ... ... Mitchell BD, et al. Ischemic stroke is associated with the ABO locus: the EuroCLOT study. Annals of Neurology. 73: 16-31. PMID 23381943 DOI: 10.1002/Ana.23838 |
0.386 |
|
| 2013 |
Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, ... ... Mitchell BD, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Human Molecular Genetics. 22: 1663-78. PMID 23303523 DOI: 10.1093/Hmg/Dds555 |
0.39 |
|
| 2013 |
Hochberg MC, Yerges-Armstrong L, Yau M, Mitchell BD. Genetic epidemiology of osteoarthritis: recent developments and future directions. Current Opinion in Rheumatology. 25: 192-7. PMID 23249833 DOI: 10.1097/Bor.0B013E32835Cfb8E |
0.315 |
|
| 2013 |
Koller DL, Zheng HF, Karasik D, Yerges-Armstrong L, Liu CT, McGuigan F, Kemp JP, Giroux S, Lai D, Edenberg HJ, Peacock M, Czerwinski SA, Choh AC, McMahon G, St Pourcain B, ... ... Mitchell BD, et al. Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 547-58. PMID 23074152 DOI: 10.1002/Jbmr.1796 |
0.368 |
|
| 2013 |
Hamedani AG, Cole JW, Cheng Y, Sparks MJ, O'Connell JR, Stine OC, Wozniak MA, Stern BJ, Mitchell BD, Kittner SJ. Factor V leiden and ischemic stroke risk: the Genetics of Early Onset Stroke (GEOS) study. Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association. 22: 419-23. PMID 22100829 DOI: 10.1016/J.Jstrokecerebrovasdis.2011.10.007 |
0.341 |
|
| 2013 |
Kiel DP, Yerges-Armstrong LM, Hsu Y, Stolk L, Karasik D, Loos RJF, Gudnason V, Smith A, O'Connell JR, Fu A, Fu M, Streeten EA, Cauley JA, Robbins JA, Psaty B, ... ... Mitchell BD, et al. Discovery and replication of several loci significantly associated with lean body mass: a large meta-analysis of genome wide association studies (GWAS) from the 'charge' and 'gefos' consortia Bone Abstracts. DOI: 10.1530/Boneabs.1.Pp283 |
0.332 |
|
| 2012 |
Mitchell BD, Hanson RL. Dissecting gene-environment contributions to Type 2 diabetes. Diabetes Management (London, England). 2: 375-378. PMID 24966891 DOI: 10.2217/Dmt.12.47 |
0.336 |
|
| 2012 |
van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, ... ... Mitchell BD, et al. Seventy-five genetic loci influencing the human red blood cell. Nature. 492: 369-75. PMID 23222517 DOI: 10.1038/Nature11677 |
0.335 |
|
| 2012 |
Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Mitchell BD, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/J.Ajhg.2012.08.032 |
0.332 |
|
| 2012 |
Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng YC, Fornage M, Ikram MA, Malik R, Bevan S, Thorsteinsdottir U, Nalls MA, Longstreth W, Wiggins KL, Yadav S, ... ... Mitchell BD, et al. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. The Lancet. Neurology. 11: 951-62. PMID 23041239 DOI: 10.1016/S1474-4422(12)70234-X |
0.401 |
|
| 2012 |
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, ... ... Mitchell BD, et al. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human Molecular Genetics. 21: 5329-43. PMID 22962313 DOI: 10.1093/Hmg/Dds369 |
0.347 |
|
| 2012 |
Holliday EG, Maguire JM, Evans TJ, Koblar SA, Jannes J, Sturm JW, Hankey GJ, Baker R, Golledge J, Parsons MW, Malik R, McEvoy M, Biros E, Lewis MD, Lincz LF, ... ... Mitchell BD, et al. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nature Genetics. 44: 1147-51. PMID 22941190 DOI: 10.1038/Ng.2397 |
0.394 |
|
| 2012 |
Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, ... ... Mitchell BD, et al. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry. 69: 854-60. PMID 22868939 DOI: 10.1001/Archgenpsychiatry.2012.124 |
0.695 |
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| 2012 |
Zheng HF, Tobias JH, Duncan E, Evans DM, Eriksson J, Paternoster L, Yerges-Armstrong LM, Lehtimäki T, Bergström U, Kähönen M, Leo PJ, Raitakari O, Laaksonen M, Nicholson GC, Viikari J, ... ... Mitchell BD, et al. WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. Plos Genetics. 8: e1002745. PMID 22792071 DOI: 10.1371/Journal.Pgen.1002745 |
0.347 |
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| 2012 |
Hochberg MC, Yerges-Armstrong L, Mitchell BD. Osteoarthritis susceptibility genes continue trickling in. Lancet. 380: 785-7. PMID 22763109 DOI: 10.1016/S0140-6736(12)60818-6 |
0.36 |
|
| 2012 |
Liu CT, Estrada K, Yerges-Armstrong LM, Amin N, Evangelou E, Li G, Minster RL, Carless MA, Kammerer CM, Oei L, Zhou Y, Alonso N, Dailiana Z, Eriksson J, García-Giralt N, ... ... Mitchell BD, et al. Assessment of gene-by-sex interaction effect on bone mineral density. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 27: 2051-64. PMID 22692763 DOI: 10.1002/Jbmr.1679 |
0.348 |
|
| 2012 |
Kochunov P, Glahn DC, Hong LE, Lancaster J, Curran JE, Johnson MP, Winkler AM, Holcomb HH, Kent JW, Mitchell B, Kochunov V, Olvera RL, Cole SA, Dyer TD, Moses EK, et al. P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans. Frontiers in Genetics. 3: 65. PMID 22558002 DOI: 10.3389/Fgene.2012.00065 |
0.304 |
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| 2012 |
Chen LS, Saccone NL, Culverhouse RC, Bracci PM, Chen CH, Dueker N, Han Y, Huang H, Jin G, Kohno T, Ma JZ, Przybeck TR, Sanders AR, Smith JA, Sung YJ, ... ... Mitchell BD, et al. Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25. Genetic Epidemiology. 36: 340-51. PMID 22539395 DOI: 10.1002/Gepi.21627 |
0.708 |
|
| 2012 |
Cole JW, Stine OC, Liu X, Pratap A, Cheng Y, Tallon LJ, Sadzewicz LK, Dueker N, Wozniak MA, Stern BJ, Meschia JF, Mitchell BD, Kittner SJ, O'Connell JR. Rare variants in ischemic stroke: an exome pilot study. Plos One. 7: e35591. PMID 22536414 DOI: 10.1371/Journal.Pone.0035591 |
0.761 |
|
| 2012 |
Estrada K, Styrkarsdottir U, Evangelou E, Hsu YH, Duncan EL, Ntzani EE, Oei L, Albagha OM, Amin N, Kemp JP, Koller DL, Li G, Liu CT, Minster RL, Moayyeri A, ... ... Mitchell BD, et al. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature Genetics. 44: 491-501. PMID 22504420 DOI: 10.1038/Ng.2249 |
0.336 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Mitchell BD, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.372 |
|
| 2012 |
McArdle PF, Whitcomb BW, Tanner K, Mitchell BD, Shuldiner AR, Parsa A. Association between bilirubin and cardiovascular disease risk factors: using Mendelian randomization to assess causal inference. Bmc Cardiovascular Disorders. 12: 16. PMID 22416852 DOI: 10.1186/1471-2261-12-16 |
0.308 |
|
| 2012 |
Cheng YC, Anderson CD, Bione S, Keene K, Maguire JM, Nalls M, Rasheed A, Zeginigg M, Attia J, Baker R, Barlera S, Biffi A, Bookman E, Brott TG, Brown RD, ... ... Mitchell BD, et al. Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke? Stroke; a Journal of Cerebral Circulation. 43: 980-6. PMID 22363065 DOI: 10.1161/Strokeaha.111.632075 |
0.407 |
|
| 2012 |
Wassel CL, Lamina C, Nambi V, Coassin S, Mukamal KJ, Ganesh SK, Jacobs DR, Franceschini N, Papanicolaou GJ, Gibson Q, Yanek LR, van der Harst P, Ferguson JF, Crawford DC, Waite LL, ... ... Mitchell BD, et al. Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium. Atherosclerosis. 222: 138-47. PMID 22361517 DOI: 10.1016/J.Atherosclerosis.2012.01.039 |
0.404 |
|
| 2012 |
Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, ... ... Mitchell BD, et al. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics. 90: 410-25. PMID 22325160 DOI: 10.1016/J.Ajhg.2011.12.022 |
0.407 |
|
| 2012 |
Bellenguez C, Bevan S, Gschwendtner A, Spencer CC, Burgess AI, Pirinen M, Jackson CA, Traylor M, Strange A, Su Z, Band G, Syme PD, Malik R, ... ... Mitchell BD, et al. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nature Genetics. 44: 328-33. PMID 22306652 DOI: 10.1038/Ng.1081 |
0.389 |
|
| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... ... Mitchell BD, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.405 |
|
| 2012 |
Murabito JM, White CC, Kavousi M, Sun YV, Feitosa MF, Nambi V, Lamina C, Schillert A, Coassin S, Bis JC, Broer L, Crawford DC, Franceschini N, Frikke-Schmidt R, Haun M, ... ... Mitchell BD, et al. Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circulation. Cardiovascular Genetics. 5: 100-12. PMID 22199011 DOI: 10.1161/Circgenetics.111.961292 |
0.401 |
|
| 2012 |
Liu J, Hoppman N, O'Connell JR, Wang H, Streeten EA, McLenithan JC, Mitchell BD, Shuldiner AR. A functional haplotype in EIF2AK3, an ER stress sensor, is associated with lower bone mineral density. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 27: 331-41. PMID 22028037 DOI: 10.1002/Jbmr.549 |
0.346 |
|
| 2012 |
Yerges-Armstrong L, Lu C, Hochberg M, Mitchell B, Jordan J, Renner J, McSherry T, Taverna D, Duggan D, Mysiw W, Jackson R. A genetic analysis of osteoarthritis of the knee in north american caucasians: results from the osteoarthritis initiative and Johnston County osteoarthritis project Osteoarthritis and Cartilage. 20: S46. DOI: 10.1016/J.Joca.2012.02.590 |
0.32 |
|
| 2012 |
Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, Klopp N, Baumert J, Padmanabhan S, ... ... Mitchell B, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017 |
0.347 |
|
| 2012 |
Saxena R, Elbers C, Guo Y, Peter I, Gaunt T, Mega J, Lanktree M, Tare A, Castillo B, Li Y, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight B, ... ... Mitchell B, et al. Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci The American Journal of Human Genetics. 90: 753. DOI: 10.1016/J.Ajhg.2012.03.001 |
0.31 |
|
| 2011 |
Cheng YC, O'Connell JR, Cole JW, Stine OC, Dueker N, McArdle PF, Sparks MJ, Shen J, Laurie CC, Nelson S, Doheny KF, Ling H, Pugh EW, Brott TG, Brown RD, ... ... Mitchell BD, et al. Genome-wide association analysis of ischemic stroke in young adults. G3 (Bethesda, Md.). 1: 505-14. PMID 22384361 DOI: 10.1534/G3.111.001164 |
0.735 |
|
| 2011 |
O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, Hwang SJ, Sun YV, Province MA, Aspelund T, Dehghan A, Hoffmann U, Bielak LF, Zhang Q, Eiriksdottir G, van Duijn CM, ... ... Mitchell BD, et al. Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation. 124: 2855-64. PMID 22144573 DOI: 10.1161/Circulationaha.110.974899 |
0.381 |
|
| 2011 |
Bis JC, Kavousi M, Franceschini N, Isaacs A, Abecasis GR, Schminke U, Post WS, Smith AV, Cupples LA, Markus HS, Schmidt R, Huffman JE, Lehtimäki T, Baumert J, Münzel T, ... ... Mitchell BD, et al. Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nature Genetics. 43: 940-7. PMID 21909108 DOI: 10.1038/Ng.920 |
0.36 |
|
| 2011 |
Shen H, Damcott C, Shuldiner SR, Chai S, Yang R, Hu H, Gibson Q, Ryan KA, Mitchell BD, Gong DW. Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels. Journal of Human Genetics. 56: 801-5. PMID 21900944 DOI: 10.1038/Jhg.2011.105 |
0.377 |
|
| 2011 |
Lewis JP, Fisch AS, Ryan K, O'Connell JR, Gibson Q, Mitchell BD, Shen H, Tanner K, Horenstein RB, Pakzy R, Tantry US, Bliden KP, Gurbel PA, Shuldiner AR. Paraoxonase 1 (PON1) gene variants are not associated with clopidogrel response. Clinical Pharmacology and Therapeutics. 90: 568-74. PMID 21881565 DOI: 10.1038/Clpt.2011.194 |
0.31 |
|
| 2011 |
Kilpeläinen TO, Zillikens MC, StanÄákova A, Finucane FM, Ried JS, Langenberg C, Zhang W, Beckmann JS, Luan J, Vandenput L, Styrkarsdottir U, Zhou Y, Smith AV, Zhao JH, Amin N, ... ... Mitchell BD, et al. Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Nature Genetics. 43: 753-60. PMID 21706003 DOI: 10.1038/Ng.866 |
0.38 |
|
| 2011 |
Speliotes EK, Yerges-Armstrong LM, Wu J, Hernaez R, Kim LJ, Palmer CD, Gudnason V, Eiriksdottir G, Garcia ME, Launer LJ, Nalls MA, Clark JM, Mitchell BD, Shuldiner AR, Butler JL, et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. Plos Genetics. 7: e1001324. PMID 21423719 DOI: 10.1371/Journal.Pgen.1001324 |
0.383 |
|
| 2011 |
Böger CA, Chen MH, Tin A, Olden M, Köttgen A, de Boer IH, Fuchsberger C, O'Seaghdha CM, Pattaro C, Teumer A, Liu CT, Glazer NL, Li M, O'Connell JR, Tanaka T, ... ... Mitchell BD, et al. CUBN is a gene locus for albuminuria. Journal of the American Society of Nephrology : Jasn. 22: 555-70. PMID 21355061 DOI: 10.1681/Asn.2010060598 |
0.418 |
|
| 2011 |
Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Mitchell BD, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007 |
0.401 |
|
| 2011 |
Anderson CD, Biffi A, Rahman R, Ross OA, Jagiella JM, Kissela B, Cole JW, Cortellini L, Rost NS, Cheng YC, Greenberg SM, de Bakker PI, Brown RD, Brott TG, Mitchell BD, et al. Common mitochondrial sequence variants in ischemic stroke. Annals of Neurology. 69: 471-80. PMID 20839239 DOI: 10.1002/Ana.22108 |
0.314 |
|
| 2010 |
Musunuru K, Post WS, Herzog W, Shen H, O'Connell JR, McArdle PF, Ryan KA, Gibson Q, Cheng YC, Clearfield E, Johnson AD, Tofler G, Yang Q, O'Donnell CJ, Becker DM, ... ... Mitchell BD, et al. Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease. Circulation. Cardiovascular Genetics. 3: 445-53. PMID 20858905 DOI: 10.1161/Circgenetics.109.923508 |
0.382 |
|
| 2010 |
Mitchell BD, Pollin TI. Genomic imprinting in diabetes. Genome Medicine. 2: 55. PMID 20727235 DOI: 10.1186/Gm176 |
0.329 |
|
| 2010 |
Hamedani AG, Cole JW, Mitchell BD, Kittner SJ. Meta-analysis of factor V Leiden and ischemic stroke in young adults: the importance of case ascertainment. Stroke; a Journal of Cerebral Circulation. 41: 1599-603. PMID 20616326 DOI: 10.1161/Strokeaha.110.581256 |
0.303 |
|
| 2010 |
Hoppman N, McLenithan JC, McBride DJ, Shen H, Bruder J, Bauer RL, Shaffer JR, Liu J, Streeten EA, Shuldiner AR, Kammerer CM, Mitchell BD. A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro. Bone. 47: 272-80. PMID 20450993 DOI: 10.1016/J.Bone.2010.04.607 |
0.377 |
|
| 2010 |
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Mitchell BD, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics. 42: 105-16. PMID 20081858 DOI: 10.1038/Ng.520 |
0.355 |
|
| 2010 |
Saxena R, Hivert MF, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, Lyssenko V, Bouatia-Naji N, Dupuis J, Jackson AU, Kao WH, Li M, Glazer NL, Manning AK, Luan J, ... ... Mitchell BD, et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nature Genetics. 42: 142-8. PMID 20081857 DOI: 10.1038/Ng.521 |
0.322 |
|
| 2010 |
Dotson CD, Shaw HL, Mitchell BD, Munger SD, Steinle NI. Variation in the gene TAS2R38 is associated with the eating behavior disinhibition in Old Order Amish women. Appetite. 54: 93-9. PMID 19782709 DOI: 10.1016/J.Appet.2009.09.011 |
0.357 |
|
| 2010 |
Van Hout CV, Levin AM, Rampersaud E, Shen H, O'Connell JR, Mitchell BD, Shuldiner AR, Douglas JA. Extent and distribution of linkage disequilibrium in the Old Order Amish. Genetic Epidemiology. 34: 146-50. PMID 19697356 DOI: 10.1002/Gepi.20444 |
0.34 |
|
| 2010 |
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Mitchell BD, et al. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Nature Genetics. 42: 464-464. DOI: 10.1038/Ng0510-464A |
0.326 |
|
| 2009 |
Tarasov KV, Sanna S, Scuteri A, Strait JB, Orrù M, Parsa A, Lin PI, Maschio A, Lai S, Piras MG, Masala M, Tanaka T, Post W, O'Connell JR, Schlessinger D, ... ... Mitchell BD, et al. COL4A1 is associated with arterial stiffness by genome-wide association scan. Circulation. Cardiovascular Genetics. 2: 151-8. PMID 20031579 DOI: 10.1161/Circgenetics.108.823245 |
0.353 |
|
| 2009 |
Mez JB, Cole JW, Howard TD, Macclellan LR, Stine OC, O'Connell JR, Wozniak MA, Stern BJ, Sorkin JD, Mitchell BD, Kittner SJ. Evaluation of self-reported ethnicity in a case-control population: the stroke prevention in young women study. Bmc Research Notes. 2: 260. PMID 20021678 DOI: 10.1186/1756-0500-2-260 |
0.347 |
|
| 2009 |
MacClellan LR, Howard TD, Cole JW, Stine OC, Giles WH, O'Connell JR, Wozniak MA, Stern BJ, Mitchell BD, Kittner SJ. Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study. Stroke; a Journal of Cerebral Circulation. 40: e550-7. PMID 19661472 DOI: 10.1161/Strokeaha.109.557462 |
0.339 |
|
| 2009 |
Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, et al. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. Plos Genetics. 5: e1000539. PMID 19557197 DOI: 10.1371/Journal.Pgen.1000539 |
0.383 |
|
| 2009 |
Shen H, Pollin TI, Damcott CM, McLenithan JC, Mitchell BD, Shuldiner AR. Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study. Human Genetics. 126: 567-74. PMID 19526250 DOI: 10.1007/S00439-009-0700-3 |
0.36 |
|
| 2009 |
Gschwendtner A, Bevan S, Cole JW, Plourde A, Matarin M, Ross-Adams H, Meitinger T, Wichmann E, Mitchell BD, Furie K, Slowik A, Rich SS, Syme PD, MacLeod MJ, Meschia JF, et al. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Annals of Neurology. 65: 531-9. PMID 19475673 DOI: 10.1002/Ana.21590 |
0.336 |
|
| 2009 |
Mitchell BD. Editorial: Clustering of schizophrenia with other comorbidities - What can we learn? Schizophrenia Bulletin. 35: 282-283. PMID 19176469 DOI: 10.1093/Schbul/Sbn189 |
0.311 |
|
| 2009 |
Ling H, Waterworth DM, Stirnadel HA, Pollin TI, Barter PJ, Kesäniemi YA, Mahley RW, McPherson R, Waeber G, Bersot TP, Cohen JC, Grundy SM, Mooser VE, Mitchell BD. Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. Obesity (Silver Spring, Md.). 17: 737-44. PMID 19165155 DOI: 10.1038/Oby.2008.625 |
0.398 |
|
| 2009 |
Wang Y, O'Connell JR, McArdle PF, Wade JB, Dorff SE, Shah SJ, Shi X, Pan L, Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC, ... ... Mitchell BD, et al. From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proceedings of the National Academy of Sciences of the United States of America. 106: 226-31. PMID 19114657 DOI: 10.1073/Pnas.0808358106 |
0.391 |
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| 2009 |
Shaffer JR, Kammerer CM, Bruder JM, Cole SA, Dyer TD, Almasy L, Maccluer JW, Blangero J, Bauer RL, Mitchell BD. Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults. Calcified Tissue International. 84: 75-84. PMID 19067020 DOI: 10.1007/S00223-008-9197-3 |
0.3 |
|
| 2008 |
Rampersaud E, Mitchell BD, Naj AC, Pollin TI. Investigating parent of origin effects in studies of type 2 diabetes and obesity. Current Diabetes Reviews. 4: 329-39. PMID 18991601 DOI: 10.2174/157339908786241179 |
0.309 |
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| 2008 |
Rampersaud E, Bielak LF, Parsa A, Shen H, Post W, Ryan KA, Donnelly P, Rumberger JA, Sheedy PF, Peyser PA, Shuldiner AR, Mitchell BD. The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults. American Journal of Epidemiology. 168: 1016-23. PMID 18805900 DOI: 10.1093/Aje/Kwn211 |
0.318 |
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| 2008 |
McArdle PF, Parsa A, Chang YPC, Weir MR, O'Connell JR, Mitchell BD, Shuldiner AR. Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in Old Order Amish Arthritis and Rheumatism. 58: 2874-2881. PMID 18759275 DOI: 10.1002/Art.23752 |
0.356 |
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| 2008 |
Cole JW, Brown DW, Giles WH, Stine OC, O'Connell JR, Mitchell BD, Sorkin JD, Wozniak MA, Stern BJ, Sparks MJ, Dobbins MT, Shoffner LT, Zappala NK, Reinhart LJ, Kittner SJ. Ischemic stroke risk, smoking, and the genetics of inflammation in a biracial population: the stroke prevention in young women study. Thrombosis Journal. 6: 11. PMID 18727828 DOI: 10.1186/1477-9560-6-11 |
0.36 |
|
| 2008 |
Chen WM, Erdos MR, Jackson AU, Saxena R, Sanna S, Silver KD, Timpson NJ, Hansen T, Orrù M, Grazia Piras M, Bonnycastle LL, Willer CJ, Lyssenko V, Shen H, Kuusisto J, ... ... Mitchell BD, et al. Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. The Journal of Clinical Investigation. 118: 2620-8. PMID 18521185 DOI: 10.1172/Jci34566 |
0.343 |
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| 2008 |
Arnaud-Lopez L, Usala G, Ceresini G, Mitchell BD, Pilia MG, Piras MG, Sestu N, Maschio A, Busonero F, Albai G, Dei M, Lai S, Mulas A, Crisponi L, Tanaka T, et al. Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. American Journal of Human Genetics. 82: 1270-80. PMID 18514160 DOI: 10.1016/J.Ajhg.2008.04.019 |
0.327 |
|
| 2008 |
Mitchell BD, McArdle PF, Shen H, Rampersaud E, Pollin TI, Bielak LF, Jaquish C, Douglas JA, Roy-Gagnon MH, Sack P, Naglieri R, Hines S, Horenstein RB, Chang YP, Post W, et al. The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. American Heart Journal. 155: 823-8. PMID 18440328 DOI: 10.1016/J.Ahj.2008.01.019 |
0.313 |
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| 2008 |
Hong LE, Wonodi I, Stine OC, Mitchell BD, Thaker GK. Evidence of Missense Mutations on the Neuregulin 1 Gene Affecting Function of Prepulse Inhibition Biological Psychiatry. 63: 17-23. PMID 17631867 DOI: 10.1016/J.Biopsych.2007.05.011 |
0.303 |
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| 2007 |
Shaffer JR, Kammerer CM, Rainwater DL, O'Leary DH, Bruder JM, Bauer RL, Mitchell BD. Decreased bone mineral density is correlated with increased subclinical atherosclerosis in older, but not younger, Mexican American women and men: the San Antonio Family Osteoporosis Study. Calcified Tissue International. 81: 430-41. PMID 17992559 DOI: 10.1007/S00223-007-9079-0 |
0.305 |
|
| 2007 |
Cole JW, Naj AC, O'Connell JR, Stine OC, Sorkin JD, Wozniak MA, Stern BJ, Yepes M, Lawrence DA, Reinhart LJ, Strickland DK, Mitchell BD, Kittner SJ. Neuroserpin polymorphisms and stroke risk in a biracial population: the stroke prevention in young women study. Bmc Neurology. 7: 37. PMID 17961231 DOI: 10.1186/1471-2377-7-37 |
0.333 |
|
| 2007 |
McArdle PF, Dytch H, O'Connell JR, Shuldiner AR, Mitchell BD, Abney M. Homozygosity by descent mapping of blood pressure in the Old Order Amish: evidence for sex specific genetic architecture. Bmc Genetics. 8: 66. PMID 17908314 DOI: 10.1186/1471-2156-8-66 |
0.308 |
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| 2007 |
Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YP, Ott SH, Zhang L, Zhao Y, Mitchell BD, O'Connell J, Shuldiner AR. Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations. Diabetes. 56: 3053-62. PMID 17846126 DOI: 10.2337/Db07-0457 |
0.355 |
|
| 2007 |
MacClellan LR, Giles W, Cole J, Wozniak M, Stern B, Mitchell BD, Kittner SJ. Probable migraine with visual aura and risk of ischemic stroke: The stroke prevention in young women study Stroke. 38: 2438-2445. PMID 17690308 DOI: 10.1161/Strokeaha.107.488395 |
0.341 |
|
| 2007 |
Hsueh WC, Silver KD, Pollin TI, Bell CJ, O'Connell JR, Mitchell BD, Shuldiner AR. A genome-wide linkage scan of insulin level derived traits: the Amish Family Diabetes Study. Diabetes. 56: 2643-8. PMID 17646211 DOI: 10.2337/Db06-1023 |
0.327 |
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| 2007 |
Post W, Shen H, Damcott C, Arking DE, Kao WHL, Sack PA, Ryan KA, Chakravarti A, Mitchell BD, Shuldiner AR. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the Old Order Amish Human Heredity. 64: 214-219. PMID 17565224 DOI: 10.1159/000103630 |
0.374 |
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| 2007 |
Roberts CG, Shen H, Mitchell BD, Damcott CM, Shuldiner AR, Rodriguez A. Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women. Human Heredity. 64: 107-13. PMID 17476110 DOI: 10.1159/000101962 |
0.35 |
|
| 2007 |
Shen H, Bielak LF, Streeten EA, Ryan KA, Rumberger JA, Sheedy PF, Shuldiner AR, Peyser PA, Mitchell BD. Relationship between vascular calcification and bone mineral density in the Old-Order Amish Calcified Tissue International. 80: 244-250. PMID 17431532 DOI: 10.1007/S00223-007-9006-4 |
0.323 |
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| 2007 |
Fu M, Sabra MM, Damcott C, Pollin TI, Ma L, Ott S, Shelton JC, Shi X, Reinhart L, O'Connell J, Mitchell BD, Baier LJ, Shuldiner AR. Evidence that Rho guanine nucleotide exchange factor 11 (ARHGEF11) on 1q21 is a type 2 diabetes susceptibility gene in the Old Order Amish Diabetes. 56: 1363-1368. PMID 17369523 DOI: 10.2337/Db06-1421 |
0.359 |
|
| 2007 |
Owen KR, Groves CJ, Hanson RL, Knowler WC, Shuldiner AR, Elbein SC, Mitchell BD, Froguel P, Ng MC, Chan JC, Jia W, Deloukas P, Hitman GA, Walker M, Frayling TM, et al. Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects. Diabetes. 56: 879-83. PMID 17327460 DOI: 10.2337/Db06-0930 |
0.385 |
|
| 2007 |
Ioannidis JP, Ng MY, Sham PC, Zintzaras E, Lewis CM, Deng HW, Econs MJ, Karasik D, Devoto M, Kammerer CM, Spector T, Andrew T, Cupples LA, Duncan EL, Foroud T, ... ... Mitchell BD, et al. Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 173-83. PMID 17228994 DOI: 10.1359/Jbmr.060806 |
0.301 |
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| 2006 |
Damcott CM, Pollin TI, Reinhart LJ, Ott SH, Shen H, Silver KD, Mitchell BD, Shuldiner AR. Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes. 55: 2654-9. PMID 16936218 DOI: 10.2337/Db06-0338 |
0.364 |
|
| 2006 |
Zeggini E, Damcott CM, Hanson RL, Karim MA, Rayner NW, Groves CJ, Baier LJ, Hale TC, Hattersley AT, Hitman GA, Hunt SE, Knowler WC, Mitchell BD, Ng MC, O'Connell JR, et al. Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q. Diabetes. 55: 2541-8. PMID 16936202 DOI: 10.2337/Db06-0088 |
0.383 |
|
| 2006 |
MacClellan LR, Mitchell BD, Cole JW, Wozniak MA, Stern BJ, Giles WH, Brown DW, Sparks MJ, Kittner SJ. Familial aggregation of ischemic stroke in young women: the Stroke Prevention in Young Women Study. Genetic Epidemiology. 30: 602-8. PMID 16868965 DOI: 10.1002/Gepi.20171 |
0.304 |
|
| 2006 |
Song Q, Cole JW, O'Connell JR, Stine OC, Gallagher M, Giles WH, Mitchell BD, Wozniak MA, Stern BJ, Sorkin JD, McArdle PF, Naj AC, Xu Q, Gibbons GH, Kittner SJ. Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study. Human Molecular Genetics. 15: 2468-78. PMID 16835261 DOI: 10.1093/Hmg/Ddl169 |
0.407 |
|
| 2006 |
Guo X, Saad MF, Langefeld CD, Williams AH, Cui J, Taylor KD, Norris JM, Jinagouda S, Darwin CH, Mitchell BD, Bergman RN, Sutton B, Chen YD, Wagenknecht LE, Bowden DW, et al. Genome-wide linkage of plasma adiponectin reveals a major locus on chromosome 3q distinct from the adiponectin structural gene: the IRAS family study. Diabetes. 55: 1723-30. PMID 16731835 DOI: 10.2337/Db05-0428 |
0.35 |
|
| 2006 |
Silver KD, Magnuson VL, Tolea M, Wang J, Hagopian WA, Mitchell BD. Association of a polymorphism in the betacellulin gene with type 1 diabetes mellitus in two populations. Journal of Molecular Medicine (Berlin, Germany). 84: 616-23. PMID 16683131 DOI: 10.1007/S00109-006-0052-6 |
0.338 |
|
| 2006 |
Kharlip J, Naglieri R, Mitchell BD, Ryan KA, Donner TW. Screening for silent coronary heart disease in type 2 diabetes: clinical application of American Diabetes Association guidelines. Diabetes Care. 29: 692-4. PMID 16505528 DOI: 10.2337/Diacare.29.03.06.Dc05-1374 |
0.314 |
|
| 2005 |
Mentuccia D, Thomas MJ, Coppotelli G, Reinhart LJ, Mitchell BD, Shuldiner AR, Celi FS. The Thr92Ala deiodinase type 2 (DIO2) variant is not associated with type 2 diabetes or indices of insulin resistance in the old order of Amish. Thyroid : Official Journal of the American Thyroid Association. 15: 1223-7. PMID 16356084 DOI: 10.1089/Thy.2005.15.1223 |
0.356 |
|
| 2005 |
Steinle NI, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish Journal of Clinical Endocrinology and Metabolism. 90: 6672-6677. PMID 16204371 DOI: 10.1210/Jc.2005-0549 |
0.378 |
|
| 2005 |
Brown LB, Streeten EA, Shapiro JR, McBride D, Shuldiner AR, Peyser PA, Mitchell BD. Genetic and environmental influences on bone mineral density in pre- and post-menopausal women. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 16: 1849-56. PMID 15997421 DOI: 10.1007/S00198-005-1948-7 |
0.301 |
|
| 2005 |
Damcott CM, Ott SH, Pollin TI, Reinhart LJ, Wang J, O'connell JR, Mitchell BD, Shuldiner AR. Genetic variation in adiponectin receptor 1 and adiponectin receptor 2 is associated with type 2 diabetes in the Old Order Amish. Diabetes. 54: 2245-50. PMID 15983228 DOI: 10.2337/Diabetes.54.7.2245 |
0.355 |
|
| 2005 |
Silver K, Tolea M, Wang J, Pollin TI, Yao F, Mitchell BD. The exon 1 Cys7Gly polymorphism within the betacellulin gene is associated with type 2 diabetes in African Americans. Diabetes. 54: 1179-84. PMID 15793259 DOI: 10.2337/Diabetes.54.4.1179 |
0.333 |
|
| 2005 |
Johnson L, Luke A, Adeyemo A, Deng HW, Mitchell BD, Comuzzie AG, Cole SA, Blangero J, Perola M, Teare MD. Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p. International Journal of Obesity (2005). 29: 413-9. PMID 15685251 DOI: 10.1038/Sj.Ijo.0802817 |
0.32 |
|
| 2005 |
Sorkin J, Post W, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Exploring the genetics of longevity in the Old Order Amish Mechanisms of Ageing and Development. 126: 347-350. PMID 15621217 DOI: 10.1016/J.Mad.2004.08.027 |
0.331 |
|
| 2005 |
Rich SS, Bowden DW, Haffner SM, Norris JM, Saad MF, Mitchell BD, Rotter JI, Langefeld CD, Hedrick CC, Wagenknecht LE, Bergman RN. A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study. Diabetes. 54: 290-5. PMID 15616041 DOI: 10.2337/Diabetes.54.1.290 |
0.302 |
|
| 2005 |
Pollin TI, Tanner K, O'connell JR, Ott SH, Damcott CM, Shuldiner AR, McLenithan JC, Mitchell BD. Linkage of plasma adiponectin levels to 3q27 explained by association with variation in the APM1 gene. Diabetes. 54: 268-74. PMID 15616038 DOI: 10.2337/Diabetes.54.1.268 |
0.357 |
|
| 2005 |
Johnson L, Luke A, Deng H, Mitchell BD, Comuzzie AG, Cole SA, Blangero J, Perola M, Teare MD. Erratum: Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p International Journal of Obesity. 29: 878-878. DOI: 10.1038/Sj.Ijo.0802966 |
0.302 |
|
| 2004 |
Cole JW, Roberts SC, Gallagher M, Giles WH, Mitchell BD, Steinberg KK, Wozniak MA, Macko RF, Reinhart LJ, Kittner SJ. Thrombomodulin Ala455Val Polymorphism and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study. Bmc Neurology. 4: 21. PMID 15574195 DOI: 10.1186/1471-2377-4-21 |
0.359 |
|
| 2004 |
Damcott CM, Hoppman N, Ott SH, Reinhart LJ, Wang J, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Polymorphisms in both promoters of hepatocyte nuclear factor 4-alpha are associated with type 2 diabetes in the Amish. Diabetes. 53: 3337-41. PMID 15561969 DOI: 10.2337/Diabetes.53.12.3337 |
0.357 |
|
| 2004 |
Fu M, Damcott CM, Sabra M, Pollin TI, Ott SH, Wang J, Garant MJ, O'Connell JR, Mitchell BD, Shuldiner AR. Polymorphism in the calsequestrin 1 (CASQ1) gene on chromosome 1q21 is associated with type 2 diabetes in the old order Amish. Diabetes. 53: 3292-9. PMID 15561962 DOI: 10.2337/Diabetes.53.12.3292 |
0.359 |
|
| 2004 |
Kammerer CM, Dualan AA, Samollow PB, Périssé ARS, Bauer RL, MacCluer JW, O'Leary DH, Mitchell BD. Bone mineral density, carotid artery intimal medial thickness, and the vitamin D receptor BsmI polymorphism in Mexican American women Calcified Tissue International. 75: 292-298. PMID 15549643 DOI: 10.1007/S00223-004-0215-9 |
0.329 |
|
| 2004 |
Brown LB, Streeten EA, Shuldiner AR, Almasy LA, Peyser PA, Mitchell BD. Assessment of sex-specific genetic and environmental effects on bone mineral density. Genetic Epidemiology. 27: 153-61. PMID 15305331 DOI: 10.1002/Gepi.20009 |
0.313 |
|
| 2004 |
Rich SS, Bowden DW, Haffner SM, Norris JM, Saad MF, Mitchell BD, Rotter JI, Langefeld CD, Wagenknecht LE, Bergman RN. Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study. Diabetes. 53: 1866-75. PMID 15220212 DOI: 10.2337/Diabetes.53.7.1866 |
0.331 |
|
| 2004 |
Steinle NI, Kazlauskaite R, Imumorin IG, Hsueh WC, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Variation in the lamin A/C gene: associations with metabolic syndrome. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1708-13. PMID 15205219 DOI: 10.1161/01.Atv.0000136384.53705.C9 |
0.329 |
|
| 2004 |
Pollin TI, Hsueh WC, Steinle NI, Snitker S, Shuldiner AR, Mitchell BD. A genome-wide scan of serum lipid levels in the Old Order Amish. Atherosclerosis. 173: 89-96. PMID 15177127 DOI: 10.1016/J.Atherosclerosis.2003.11.012 |
0.315 |
|
| 2003 |
Mitchell BD, Kammerer CM, Schneider JL, Perez R, Bauer RL. Genetic and environmental determinants of bone mineral density in Mexican Americans: results from the San Antonio Family Osteoporosis Study. Bone. 33: 839-46. PMID 14623060 DOI: 10.1016/S8756-3282(03)00246-1 |
0.326 |
|
| 2003 |
Maser RE, Mitchell BD, Vinik AI, Freeman R. The association between cardiovascular autonomic neuropathy and mortality in individuals with diabetes a meta-analysis Diabetes Care. 26: 1895-1901. PMID 12766130 DOI: 10.2337/Diacare.26.6.1895 |
0.317 |
|
| 2003 |
Vinik AI, Maser RE, Mitchell BD, Freeman R. Diabetic autonomic neuropathy Diabetes Care. 26: 1553-1579. PMID 12716821 DOI: 10.2337/Diacare.26.5.1553 |
0.3 |
|
| 2003 |
Henkin L, Bergman RN, Bowden DW, Ellsworth DL, Haffner SM, Langefeld CD, Mitchell BD, Norris JM, Rewers M, Saad MF, Stamm E, Wagenknecht LE, Rich SS. Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods. Annals of Epidemiology. 13: 211-7. PMID 12684185 DOI: 10.1016/S1047-2797(02)00412-X |
0.308 |
|
| 2003 |
Hsueh WC, St Jean PL, Mitchell BD, Pollin TI, Knowler WC, Ehm MG, Bell CJ, Sakul H, Wagner MJ, Burns DK, Shuldiner AR. Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24. Diabetes. 52: 550-7. PMID 12540634 DOI: 10.2337/Diabetes.52.2.550 |
0.312 |
|
| 2003 |
Blumenthal JB, Andersen RE, Mitchell BD, Seibert MJ, Yang H, Herzog H, Beamer BA, Franckowiak SC, Walston JD. Novel neuropeptide Y1 and Y5 receptor gene variants: associations with serum triglyceride and high-density lipoprotein cholesterol levels. Clinical Genetics. 62: 196-202. PMID 12220433 DOI: 10.1034/J.1399-0004.2002.620302.X |
0.323 |
|
| 2002 |
Steinle NI, Hsueh WC, Snitker S, Pollin TI, Sakul H, St Jean PL, Bell CJ, Mitchell BD, Shuldiner AR. Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis. The American Journal of Clinical Nutrition. 75: 1098-106. PMID 12036819 DOI: 10.1093/Ajcn/75.6.1098 |
0.3 |
|
| 2002 |
Mitchell BD, Imumorin IG. Genetic determinants of diabetes and atherosclerosis Current Atherosclerosis Reports. 4: 193-198. PMID 11931716 DOI: 10.1007/S11883-002-0019-1 |
0.34 |
|
| 2001 |
Hsueh WC, Göring HHH, Blangero J, Mitchell BD. Replication of linkage to quantitative trait loci: Variation in location and magnitude of the lod score Genetic Epidemiology. 21. PMID 11793721 DOI: 10.1002/Gepi.2001.21.S1.S473 |
0.316 |
|
| 2001 |
Mitchell BD. Introduction: Association and TDT analyses of quantitative traits Genetic Epidemiology. 21. PMID 11793694 DOI: 10.1002/Gepi.2001.21.S1.S339 |
0.337 |
|
| 2001 |
Wang XL, Rainwater DL, VandeBerg JF, Mitchell BD, Mahaney MC. Genetic contributions to plasma total antioxidant activity Arteriosclerosis, Thrombosis, and Vascular Biology. 21: 1190-1195. PMID 11451750 DOI: 10.1161/Hq0701.092146 |
0.351 |
|
| 2001 |
Hsueh WC, Cole SA, Shuldiner AR, Beamer BA, Blangero J, Hixson JE, MacCluer JW, Mitchell BD. Interactions between variants in the β3-adrenergic receptor and peroxisome proliferator-activated receptor-γ2 genes and obesity Diabetes Care. 24: 672-677. PMID 11315829 DOI: 10.2337/Diacare.24.4.672 |
0.359 |
|
| 2001 |
Hsueh WC, Mitchell BD, Schneider JL, St Jean PL, Pollin TI, Ehm MG, Wagner MJ, Burns DK, Sakul H, Bell CJ, Shuldiner AR. Genome-wide scan of obesity in the Old Order Amish. The Journal of Clinical Endocrinology and Metabolism. 86: 1199-205. PMID 11238509 DOI: 10.1210/Jcem.86.3.7358 |
0.319 |
|
| 2000 |
Hsueh WC, Mitchell BD, Hixson JE, Rainwater DL. Effects of the apoE polymorphism on plasma lipoproteins in Mexican Americans Annals of Epidemiology. 10: 524-531. PMID 11118932 DOI: 10.1016/S1047-2797(00)00074-0 |
0.319 |
|
| 2000 |
Rainwater DL, Mitchell BD, Comuzzie AG, VandeBerg JL, Stern MP, MacCluer JW. Associations among 5-year changes in weight, physical activity, and cardiovascular disease risk factors in Mexican Americans American Journal of Epidemiology. 152: 974-982. PMID 11092439 DOI: 10.1093/Aje/152.10.974 |
0.313 |
|
| 2000 |
Mitchell BD, Cole SA, Hsueh WC, Comuzzie AG, Blangero J, MacCluer JW, Hixson JE. Linkage of serum insulin concentrations to chromosome 3p in Mexican Americans Diabetes. 49: 513-516. PMID 10868977 DOI: 10.2337/Diabetes.49.3.513 |
0.327 |
|
| 2000 |
Hsueh WC, Mitchell BD, Schneider JL, Wagner MJ, Bell CJ, Nanthakumar E, Shuldiner AR. QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish. Circulation. 101: 2810-6. PMID 10859286 DOI: 10.1161/01.Cir.101.24.2810 |
0.319 |
|
| 2000 |
Hsueh WC, Mitchell BD, Aburomia R, Pollin T, Sakul H, Gelder Ehm M, Michelsen BK, Wagner MJ, St Jean PL, Knowler WC, Burns DK, Bell CJ, Shuldiner AR. Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study. Diabetes Care. 23: 595-601. PMID 10834415 DOI: 10.2337/Diacare.23.5.595 |
0.322 |
|
| 2000 |
Cole SA, Mitchell BD, Hsueh WC, Pineda P, Beamer BA, Shuldiner AR, Comuzzie AG, Blangero J, Hixson JE. The Pro12Ala variant of peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) is associated with measures of obesity in Mexican Americans International Journal of Obesity. 24: 522-524. PMID 10805513 DOI: 10.1038/Sj.Ijo.0801210 |
0.353 |
|
| 2000 |
Mitchell BD, Cole SA, Bauer RL, Iturria SJ, Rodriguez EA, Blangero J, MacCluer JW, Hixson JE. Genes influencing variation in serum osteocalcin concentrations are linked to markers on chromosomes 16q and 20q. The Journal of Clinical Endocrinology and Metabolism. 85: 1362-6. PMID 10770166 DOI: 10.1210/Jcem.85.4.6571 |
0.311 |
|
| 1999 |
Watanabe RM, Ghosh S, Birznieks G, Duren WL, Mitchell BD. Application of an ordered subset analysis approach to the genetics of alcoholism Genetic Epidemiology. 17. PMID 10597467 DOI: 10.1002/Gepi.1370170765 |
0.314 |
|
| 1999 |
Hixson JE, Almasy L, Cole S, Birnbaum S, Mitchell BD, Mahaney MC, Stern MP, Maccluer JW, Blangero J, Comuzzie AG. Normal variation in leptin levels is associated with polymorphisms in the proopiomelanocortin gene, POMC Journal of Clinical Endocrinology and Metabolism. 84: 3187-3191. PMID 10487685 DOI: 10.1210/Jcem.84.9.5951 |
0.373 |
|
| 1999 |
Mitchell BD, Cole SA, Comuzzie AG, Almasy L, Blangero J, MacCluer JW, Hixson JE. A quantitative trait locus influencing BMI maps to the region of the adrenergic receptor Diabetes. 48: 1863-1867. PMID 10480620 DOI: 10.2337/Diabetes.48.9.1863 |
0.336 |
|
| 1999 |
MacCluer JW, Stern MP, Almasy L, Atwood LA, Blangero J, Comuzzie AG, Dyke B, Haffner SM, Henkel RD, Hixson JE, Kammerer CM, Mahaney MC, Mitchell BD, Rainwater DL, Samollow PB, et al. Genetics of atherosclerosis risk factors in Mexican Americans. Nutrition Reviews. 57: S59-65. PMID 10391028 DOI: 10.1111/J.1753-4887.1999.Tb01790.X |
0.308 |
|
| 1999 |
Mitchell BD, Almasy LA, Rainwater DL, Schneider JL, Blangero J, Stern MP, MacCluer JW. Diabetes and hypertension in Mexican American families: Relation to cardiovascular risk American Journal of Epidemiology. 149: 1047-1056. PMID 10355381 DOI: 10.1093/Oxfordjournals.Aje.A009750 |
0.329 |
|
| 1999 |
Duggirala R, Mitchell BD, Blangero J, Stern MP. Genetic determinants of variation in gallbladder disease in the Mexican- American population Genetic Epidemiology. 16: 191-204. PMID 10030401 DOI: 10.1002/(Sici)1098-2272(1999)16:2<191::Aid-Gepi6>3.0.Co;2-6 |
0.346 |
|
| 1998 |
Goksel DL, Fischbach K, Duggirala R, Mitchell BD, Aguilar-Bryan L, Blangero J, Stern MP, O'Connell P. Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia Human Genetics. 103: 280-285. PMID 9799081 DOI: 10.1007/S004390050817 |
0.355 |
|
| 1998 |
Mitchell BD, Blangero J, Comuzzie AG, Almasy LA, Shuldiner AR, Silver K, Stern MP, MacCluer JW, Hixson JE. A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans Journal of Clinical Investigation. 101: 584-587. PMID 9449691 DOI: 10.1172/Jci512 |
0.318 |
|
| 1997 |
Silver K, Mitchell BD, Walston J, Sorkin JD, Stern MP, Roth J, Shuldiner AR. TRP64ARG β3-adrenergic receptor and obesity in Mexican Americans Human Genetics. 101: 306-311. PMID 9439659 DOI: 10.1007/S004390050633 |
0.381 |
|
| 1997 |
Rainwater DL, Mitchell BD, Mahaney MC, Haffner SM. Genetic relationship between measures of HDL phenotypes and insulin concentrations Arteriosclerosis, Thrombosis, and Vascular Biology. 17: 3414-3419. PMID 9437187 DOI: 10.1161/01.Atv.17.12.3414 |
0.309 |
|
| 1997 |
Comuzzie AG, Hixson JE, Almasy L, Mitchell BD, Mahaney MC, Dyer TD, Stern MP, MacCluer JW, Blangero J. A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 Nature Genetics. 15: 273-276. PMID 9054940 DOI: 10.1038/Ng0397-273 |
0.344 |
|
| 1996 |
Mitchell BD, Kammerer CM, Blangero J, Mahaney MC, Rainwater DL, Dyke B, Hixson JE, Henkel RD, Sharp RM, Comuzzie AG, Vandeberg JL, Stern MP, MacCluer JW. Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans: The San Antonio Family Heart Study Circulation. 94: 2159-2170. PMID 8901667 DOI: 10.1161/01.Cir.94.9.2159 |
0.363 |
|
| 1996 |
Stern MP, Duggirala R, Mitchell BD, Reinhart LJ, Shivakumar S, Shipman PA, Uresandi OC, Benavides E, Blangero J, O'Connell P. Evidence for linkage of regions on chromosomes 6 and 11 to plasma glucose concentrations in Mexican Americans. Genome Research. 6: 724-34. PMID 8858347 DOI: 10.1101/Gr.6.8.724 |
0.339 |
|
| 1996 |
Comuzzie AG, Blangero J, Mahaney MC, Haffner SM, Mitchell BD, Stern MP, MacCluer JW. Genetic and environmental correlations among hormone levels and measures of body fat accumulation and topography. The Journal of Clinical Endocrinology and Metabolism. 81: 597-600. PMID 8636274 DOI: 10.1210/Jcem.81.2.8636274 |
0.331 |
|
| 1996 |
Stern MP, Mitchell BD, Blangero J, Reinhart L, Krammerer CM, Harrison CR, Shipman PA, O'Connell P, Frazier ML, MacCluer JW. Evidence for a major gene for type II diabetes and linkage analyses with selected candidate genes in Mexican-Americans. Diabetes. 45: 563-8. PMID 8621004 DOI: 10.2337/Diab.45.5.563 |
0.335 |
|
| 1996 |
Mitchell BD, Kammerer CM, Mahaney MC, Blangero J, Comuzzie AG, Atwood LD, Haffner SM, Stern MP, MacCluer JW. Genetic analysis of the IRS: Pleiotropic effects of genes influencing insulin levels on lipoprotein and obesity measures Arteriosclerosis, Thrombosis, and Vascular Biology. 16: 281-288. PMID 8620344 DOI: 10.1161/01.Atv.16.2.281 |
0.318 |
|
| 1995 |
Comuzzie AG, Blangero J, Mahaney MC, Mitchell BD, Hixson JE, Samollow PB, Stern MP, MacCluer JW. Major gene with sex-specific effects influences fat mass in Mexican Americans Genetic Epidemiology. 12: 475-488. PMID 8557180 DOI: 10.1002/Gepi.1370120505 |
0.326 |
|
| 1995 |
Mitchell BD, Kammerer CM, Hixson JE, Atwood LD, Hackleman S, Blangero J, Haffner SM, Stern MP, MacCluer JW. Evidence for a major gene affecting postchallenge insulin levels in Mexican-Americans Diabetes. 44: 284-289. PMID 7883115 DOI: 10.2337/Diab.44.3.284 |
0.301 |
|
| 1995 |
Mitchell BD, Villalpando CG, Perez BA, Garcia MS, Valdez R, Stern MP. Myocardial infarction and cardiovascular risk factors in Mexico City and San Antonio, Texas Arteriosclerosis, Thrombosis, and Vascular Biology. 15: 721-725. PMID 7773724 DOI: 10.1161/01.Atv.15.6.721 |
0.324 |
|
| 1995 |
Mitchell BD, Kammerer CM, O'Connell P, Harrison CR, Manire M, Shipman P, Moyer MP, Stern MP, Frazier ML. Evidence for linkage of postchallenge insulin levels with intestinal fatty acid-binding protein (FABP2) in Mexican-Americans. Diabetes. 44: 1046-53. PMID 7657027 DOI: 10.2337/Diab.44.9.1046 |
0.312 |
|
| 1994 |
Haffner SM, Mitchell BD, Moss SE, Stern MP, Hazuda HP, Patterson J, Van Heuven WA, Klein R. Is there an ethnic difference in the effect of risk factors for diabetic retinopathy? Annals of Epidemiology. 3: 2-8. PMID 8287152 DOI: 10.1016/1047-2797(93)90003-M |
0.308 |
|
| 1994 |
Mitchell BD, Kammerer CM, Reinhart LJ, Stern MP. NIDDM in Mexican-American families: Heterogeneity by age of onset Diabetes Care. 17: 567-573. PMID 8082526 DOI: 10.2337/Diacare.17.6.567 |
0.311 |
|
| 1993 |
Morales PA, Mitchell BD, Valdez RA, Hazuda HP, Stern MP, Haffner SM. Incidence of NIDDM and impaired glucose tolerance in hypertensive subjects: The San Antonio heart study Diabetes. 42: 154-161. PMID 8420812 DOI: 10.2337/Diab.42.1.154 |
0.305 |
|
| 1993 |
Haffner SM, Gonzales C, Valdez RA, Mykkänen L, Hazuda HP, Mitchell BD, Monterrosa A, Stern MP. Is microalbuminuria part of the prediabetic state? The Mexico City Diabetes Study Diabetologia: Clinical and Experimental Diabetes and Metabolism. 36: 1002-1006. PMID 8243847 DOI: 10.1007/Bf02374491 |
0.311 |
|
| 1992 |
Stern MP, Gonzalez C, Mitchell BD, Villalpando E, Haffner SM, Hazuda HP. Genetic and environmental determinants of type II diabetes in Mexico City and San Antonio Diabetes. 41: 484-492. PMID 1607073 DOI: 10.2337/Diab.41.4.484 |
0.352 |
|
| 1992 |
Haffner SM, Mitchell BD, Valdez RA, Hazuda HP, Morales PA, Stem MP. Eight-year incidence of hypertension in mexican-americans and non-hispanic whites the san antonio heart study American Journal of Hypertension. 5: 147-153. PMID 1575941 DOI: 10.1093/Ajh/5.3.147 |
0.3 |
|
| 1992 |
Stern MP, Mitchell BD, Haffner SM, Hazuda HP. Does glycemic control of type II diabetes suffice to control diabetic dyslipidemia? A community perspective Diabetes Care. 15: 638-644. PMID 1516483 DOI: 10.2337/Diacare.15.5.638 |
0.301 |
|
| 1992 |
Mitchell BD, Haffner SM, Hazuda HP, Valdez R, Stern MP. The relation between serum insulin levels and 8-year changes in lipid, lipoprotein, and blood pressure levels American Journal of Epidemiology. 136: 12-22. PMID 1415128 DOI: 10.1093/Oxfordjournals.Aje.A116416 |
0.304 |
|
| 1992 |
Mitchell BD, Haffner SM, Hazuda HP, Patterson JK, Stern MP. Diabetes and coronary heart disease risk in Mexican Americans Annals of Epidemiology. 2: 101-106. PMID 1342250 DOI: 10.1016/1047-2797(92)90043-P |
0.326 |
|
| 1991 |
Haffner SM, Hazuda HP, Mitchell BD, Patterson JK, Stern MP. Increased incidence of type II diabetes mellitus in Mexican Americans Diabetes Care. 14: 102-108. PMID 2060411 DOI: 10.2337/Diacare.14.2.102 |
0.305 |
|
| 1991 |
Haffner SM, Mitchell BD, Hazuda HP, Stern MP. Greater influence of central distribution of adipose tissue on incidence of non-insulin-dependent diabetes in women than men American Journal of Clinical Nutrition. 53: 1312-1317. PMID 2021139 DOI: 10.1093/Ajcn/53.5.1312 |
0.313 |
|
| 1991 |
Haffner SM, Mitchell BD, Stern MP, Hazuda HP. Macrovascular complications in Mexican Americans with type II diabetes Diabetes Care. 14: 665-671. PMID 1914816 DOI: 10.2337/Diacare.14.7.665 |
0.31 |
|
| 1991 |
Stern MP, Knapp JA, Hazuda HP, Haffner SM, Patterson JK, Mitchell BD. Genetic and environmental determinants of type II diabetes in Mexican Americans: Is there a "descending limb" to the modernization/diabetes relationship? Diabetes Care. 14: 649-654. PMID 1914814 DOI: 10.2337/Diacare.14.7.649 |
0.323 |
|
| 1991 |
Ferrannini E, Haffner SM, Mitchell BD, Stern MP. Hyperinsulinaemia: the key feature of a cardiovascular and metabolic syndrome Diabetologia. 34: 416-422. PMID 1884900 DOI: 10.1007/Bf00403180 |
0.307 |
|
| 1991 |
Mitchell BD, Hazuda HP, Haffner SM, Patterson JK, Stern MP. High prevalence of angina pectoris in Mexican-American men. A population with reduced risk of myocardial infraction Annals of Epidemiology. 1: 415-426. PMID 1669522 DOI: 10.1016/1047-2797(91)90011-Z |
0.317 |
|
| 1990 |
Haffner SM, Stern MP, Katherine Kozlowski Gruber M, Hazuda HP, Mitchell BD, Patterson JK. Microalbuminuria - Potential marker for increased cardiovascular risk factors in nondiabetic subjects? Arteriosclerosis, Thrombosis, and Vascular Biology. 10: 727-731. PMID 2403300 DOI: 10.1161/01.Atv.10.5.727 |
0.313 |
|
| 1990 |
Haffner SM, Mitchell BD, Stern MP, Hazuda HP, Patterson JK. Decreased prevalence of hypertension in Mexican-Americans Hypertension. 16: 225-232. PMID 2394482 DOI: 10.1161/01.Hyp.16.3.225 |
0.313 |
|
| 1990 |
Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK. Cardiovascular Risk Factors in Confirmed Prediabetic Individuals: Does the Clock for Coronary Heart Disease Start Ticking Before the Onset of Clinical Diabetes? Jama: the Journal of the American Medical Association. 263: 2893-2898. PMID 2338751 DOI: 10.1001/Jama.1990.03440210043030 |
0.352 |
|
| 1990 |
Mitchell BD, Stern MP, Haffner SM, Hazuda HP, Patterson JK. Functional impairment in Mexican Americans and non-hispanic whites with diabetes Journal of Clinical Epidemiology. 43: 319-327. PMID 2324773 DOI: 10.1016/0895-4356(90)90118-9 |
0.308 |
|
| 1990 |
Mitchell BD, Stern MP, Haffner SM, Hazuda HP, Patterson JK. Risk factors for cardiovascular mortality in Mexican Americans and non-hispanic whites: The san antonio heart study American Journal of Epidemiology. 131: 423-433. PMID 2301352 DOI: 10.1093/Oxfordjournals.Aje.A115517 |
0.302 |
|
| 1990 |
Haffner SM, Diehl AK, Mitchell BD, Stern MP, Hazuda HP. Increased prevalence of clinical gallbladder disease in subjects with non-insulin-dependent diabetes mellitus American Journal of Epidemiology. 132: 327-335. PMID 2196792 DOI: 10.1093/Oxfordjournals.Aje.A115662 |
0.324 |
|
| 1989 |
Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK, Ferrannini E. Parental history of diabetes is associated with increased cardiovascular risk factors Arteriosclerosis. 9: 928-933. PMID 2686606 DOI: 10.1161/01.Atv.9.6.928 |
0.328 |
|
| 1989 |
Raboudi SH, Mitchell BD, Stern MP, Eifler CW, Haffner SM, Hazuda HP, Frazier ML. Type II diabetes mellitus and polymorphism of insulin-receptor gene in Mexican Americans. Diabetes. 38: 975-80. PMID 2568958 DOI: 10.2337/Diab.38.8.975 |
0.353 |
|
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