| Year |
Citation |
Score |
| 2024 |
Suzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A, Melloni GEM, Kanoni S, Rayner NW, Bocher O, Arruda AL, Sonehara K, Namba S, ... ... Zawistowski M, et al. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. PMID 38374256 DOI: 10.1038/s41586-024-07019-6 |
0.657 |
|
| 2023 |
Wang A, Shen J, Rodriguez AA, Saunders EJ, Chen F, Janivara R, Darst BF, Sheng X, Xu Y, Chou AJ, Benlloch S, Dadaev T, Brook MN, Plym A, Sahimi A, ... ... Zawistowski M, et al. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Nature Genetics. PMID 37945903 DOI: 10.1038/s41588-023-01534-4 |
0.631 |
|
| 2023 |
Kwong A, Zawistowski M, Fritsche LG, Zhan X, Bragg-Gresham J, Branham KE, Advani J, Othman M, Ratnapriya R, Teslovich TM, Stambolian D, Chew EY, Abecasis GR, Swaroop A. Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration. Human Molecular Genetics. PMID 37934784 DOI: 10.1093/hmg/ddad189 |
0.455 |
|
| 2023 |
Bastarache L, Delozier S, Pandit A, He J, Lewis A, Annis AC, LeFaive J, Denny JC, Carroll RJ, Altman RB, Hughey JJ, Zawistowski M, Peterson JF. The phenotype-genotype reference map: Improving biobank data science through replication. American Journal of Human Genetics. PMID 37607538 DOI: 10.1016/j.ajhg.2023.07.012 |
0.344 |
|
| 2023 |
Suzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A, Rayner NW, Bocher O, Ana Luiza de SVA, Sonehara K, Namba S, Lee SSK, Preuss MH, ... ... Zawistowski M, et al. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Medrxiv : the Preprint Server For Health Sciences. PMID 37034649 DOI: 10.1101/2023.03.31.23287839 |
0.66 |
|
| 2023 |
Zawistowski M, Fritsche LG, Pandit A, Vanderwerff B, Patil S, Schmidt EM, VandeHaar P, Willer CJ, Brummett CM, Kheterpal S, Zhou X, Boehnke M, Abecasis GR, Zöllner S. The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients. Cell Genomics. 3: 100257. PMID 36819667 DOI: 10.1016/j.xgen.2023.100257 |
0.679 |
|
| 2022 |
Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, ... ... Zawistowski M, et al. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192. PMID 36777996 DOI: 10.1016/j.xgen.2022.100192 |
0.683 |
|
| 2022 |
Georges A, Yang ML, Berrandou TE, Bakker MK, Dikilitas O, Kiando SR, Ma L, Satterfield BA, Sengupta S, Yu M, Deleuze JF, Dupré D, Hunker KL, Kyryachenko S, Liu L, ... ... Zawistowski M, et al. Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications. 13: 2251. PMID 35443759 DOI: 10.1038/s41467-022-29921-1 |
0.671 |
|
| 2021 |
Eijsbouts C, Zheng T, Kennedy NA, Bonfiglio F, Anderson CA, Moutsianas L, Holliday J, Shi J, Shringarpure S, Voda AI, Farrugia G, Franke A, Hübenthal M, ... ... Zawistowski M, et al. Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. Nature Genetics. 53: 1543-1552. PMID 34741163 DOI: 10.1038/s41588-021-00950-8 |
0.325 |
|
| 2021 |
Georges A, Yang ML, Berrandou TE, Bakker MK, Dikilitas O, Kiando SR, Ma L, Satterfield BA, Sengupta S, Yu M, Deleuze JF, Dupré D, Hunker KL, Kyryachenko S, Liu L, ... ... Zawistowski M, et al. Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications. 12: 6031. PMID 34654805 DOI: 10.1038/s41467-021-26174-2 |
0.67 |
|
| 2021 |
Garcia-Etxebarria K, Carbone F, Teder-Laving M, Pandit A, Holvoet L, Thijs V, Lemmens R, Bujanda L, Franke A, Zöllner S, Boehnke M, Zawistowski M, Esko T, Jan T, D'Amato M. A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses. Neurogastroenterology and Motility : the Official Journal of the European Gastrointestinal Motility Society. e14236. PMID 34378841 DOI: 10.1111/nmo.14236 |
0.638 |
|
| 2021 |
Cox CK, Pandit A, Zawistowski M, Dutta D, Narla G, Swenson CW. Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative. Female Pelvic Medicine & Reconstructive Surgery. PMID 34027909 DOI: 10.1097/SPV.0000000000001075 |
0.356 |
|
| 2021 |
Zheng T, Ellinghaus D, Juzenas S, Cossais F, Burmeister G, Mayr G, Jørgensen IF, Teder-Laving M, Skogholt AH, Chen S, Strege PR, Ito G, Banasik K, Becker T, Bokelmann F, ... ... Zawistowski M, et al. Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease. Gut. PMID 33888516 DOI: 10.1136/gutjnl-2020-323868 |
0.471 |
|
| 2021 |
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Zawistowski M, et al. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33674754 DOI: 10.1038/s41380-021-01063-8 |
0.566 |
|
| 2021 |
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Zawistowski M, et al. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33483695 DOI: 10.1038/s41380-020-01006-9 |
0.645 |
|
| 2020 |
Nielsen JB, Rom O, Surakka I, Graham SE, Zhou W, Roychowdhury T, Fritsche LG, Gagliano Taliun SA, Sidore C, Liu Y, Gabrielsen ME, Skogholt AH, Wolford B, Overton W, Zhao Y, ... ... Zawistowski M, et al. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Nature Communications. 11: 6417. PMID 33339817 DOI: 10.1038/s41467-020-20086-3 |
0.634 |
|
| 2020 |
Goldstein JA, Weinstock JS, Bastarache LA, Larach DB, Fritsche LG, Schmidt EM, Brummett CM, Kheterpal S, Abecasis GR, Denny JC, Zawistowski M. LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks. Plos Genetics. 16: e1009077. PMID 33175840 DOI: 10.1371/journal.pgen.1009077 |
0.374 |
|
| 2020 |
Richer J, Hill HL, Wang Y, Yang ML, Hunker KL, Lane J, Blackburn S, Coleman DM, Eliason J, Sillon G, D'Agostino MD, Jetty P, Mongeon FP, Laberge AM, Ryan SE, ... ... Zawistowski M, et al. Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA119313885. PMID 32938213 DOI: 10.1161/Atvbaha.119.313885 |
0.403 |
|
| 2020 |
Saw J, Yang ML, Trinder M, Tcheandjieu C, Xu C, Starovoytov A, Birt I, Mathis MR, Hunker KL, Schmidt EM, Jackson L, Fendrikova-Mahlay N, Zawistowski M, Brummett CM, Zoellner S, et al. Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Nature Communications. 11: 4432. PMID 32887874 DOI: 10.1038/S41467-020-17558-X |
0.33 |
|
| 2020 |
Zhou W, Brumpton B, Kabil O, Gudmundsson J, Thorleifsson G, Weinstock J, Zawistowski M, Nielsen JB, Chaker L, Medici M, Teumer A, Naitza S, Sanna S, Schultheiss UT, Cappola A, et al. GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. Nature Communications. 11: 3981. PMID 32769997 DOI: 10.1038/S41467-020-17718-Z |
0.37 |
|
| 2020 |
Landi MT, Bishop DT, MacGregor S, Machiela MJ, Stratigos AJ, Ghiorzo P, Brossard M, Calista D, Choi J, Fargnoli MC, Zhang T, Rodolfo M, Trower AJ, Menin C, Martinez J, ... ... Zawistowski M, et al. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics. PMID 32341527 DOI: 10.1038/S41588-020-0611-8 |
0.504 |
|
| 2019 |
Dutta D, Gagliano Taliun SA, Weinstock JS, Zawistowski M, Sidore C, Fritsche LG, Cucca F, Schlessinger D, Abecasis GR, Brummett CM, Lee S. Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test. Genetic Epidemiology. PMID 31433078 DOI: 10.1002/Gepi.22248 |
0.463 |
|
| 2019 |
Fritsche LG, Beesley LJ, VandeHaar P, Peng RB, Salvatore M, Zawistowski M, Gagliano Taliun SA, Das S, LeFaive J, Kaleba EO, Klumpner TT, Moser SE, Blanc VM, Brummett CM, Kheterpal S, et al. Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb. Plos Genetics. 15: e1008202. PMID 31194742 DOI: 10.1371/Journal.Pgen.1008202 |
0.473 |
|
| 2019 |
Graham SE, Nielsen JB, Zawistowski M, Zhou W, Fritsche LG, Gabrielsen ME, Skogholt AH, Surakka I, Hornsby WE, Fermin D, Larach DB, Kheterpal S, Brummett CM, Lee S, Kang HM, et al. Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Nature Communications. 10: 1847. PMID 31015462 DOI: 10.1038/S41467-019-09861-Z |
0.41 |
|
| 2018 |
Carlson J, Locke AE, Flickinger M, Zawistowski M, Levy S, Myers RM, Boehnke M, Kang HM, Scott LJ, Li JZ, Zöllner S. Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans. Nature Communications. 9: 3753. PMID 30218074 DOI: 10.1038/S41467-018-05936-5 |
0.64 |
|
| 2018 |
Fritsche LG, Gruber SB, Wu Z, Schmidt EM, Zawistowski M, Moser SE, Blanc VM, Brummett CM, Kheterpal S, Abecasis GR, Mukherjee B. Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative. American Journal of Human Genetics. PMID 29779563 DOI: 10.1016/J.Ajhg.2018.04.001 |
0.42 |
|
| 2018 |
Patrick M, Stuart P, Raja K, Yang J, Zawistowski M, Voorhees J, Tejasvi T, Gudjonsson J, Chandran V, Rahman P, Nair R, Gladman D, Elder J, Tsoi L. 746 Challenges and opportunities for integrating genetics and health records in risk assessment for psoriasis subtypes Journal of Investigative Dermatology. 138: S127. DOI: 10.1016/J.Jid.2018.03.756 |
0.366 |
|
| 2017 |
Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, et al. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America. PMID 29279374 DOI: 10.1073/Pnas.1705859115 |
0.702 |
|
| 2017 |
Dand N, Mucha S, Tsoi LC, Mahil SK, Stuart PE, Arnold A, Baurecht H, Burden AD, Duffin KC, Chandran V, Curtis CJ, Das S, Ellinghaus D, Ellinghaus E, Enerback C, ... ... Zawistowski M, et al. Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Human Molecular Genetics. PMID 28973304 DOI: 10.1093/Hmg/Ddx328 |
0.467 |
|
| 2017 |
Sussman JB, Wiitala WL, Zawistowski M, Hofer TP, Bentley D, Hayward RA. The Veterans Affairs Cardiac Risk Score: Recalibrating the Atherosclerotic Cardiovascular Disease Score for Applied Use. Medical Care. 55: 864-870. PMID 28763374 DOI: 10.1097/Mlr.0000000000000781 |
0.343 |
|
| 2017 |
Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S, Zawistowski M, Ellinghaus E, Barker JN, Chandran V, Dand N, Duffin KC, Enerbäck C, Esko T, Franke A, Gladman DD, et al. Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nature Communications. 8: 15382. PMID 28537254 DOI: 10.1038/Ncomms15382 |
0.494 |
|
| 2017 |
Budu-Aggrey A, Bowes J, Stuart PE, Zawistowski M, Tsoi LC, Nair R, Jadon DR, McHugh N, Korendowych E, Elder JT, Barton A, Raychaudhuri S. A rare coding allele in IFIH1 is protective for psoriatic arthritis. Annals of the Rheumatic Diseases. PMID 28501801 DOI: 10.1136/Annrheumdis-2016-210592 |
0.348 |
|
| 2016 |
Hovelson DH, Xue Z, Zawistowski M, Ehm MG, Harris EC, Stocker SL, Gross AS, Jang IJ, Ieiri I, Lee JE, Cardon LR, Chissoe SL, Abecasis G, Nelson MR. Characterization of ADME gene variation in 21 populations by exome sequencing. Pharmacogenetics and Genomics. PMID 27984508 DOI: 10.1097/Fpc.0000000000000260 |
0.393 |
|
| 2015 |
Feng S, Pistis G, Zhang H, Zawistowski M, Mulas A, Zoledziewska M, Holmen OL, Busonero F, Sanna S, Hveem K, Willer C, Cucca F, Liu DJ, Abecasis GR. Methods for association analysis and meta-analysis of rare variants in families. Genetic Epidemiology. 39: 227-38. PMID 25740221 DOI: 10.1002/Gepi.21892 |
0.416 |
|
| 2014 |
Zawistowski M, Reppell M, Wegmann D, St Jean PL, Ehm MG, Nelson MR, Novembre J, Zöllner S. Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests. European Journal of Human Genetics : Ejhg. 22: 1137-44. PMID 24398795 DOI: 10.1038/Ejhg.2013.297 |
0.426 |
|
| 2014 |
Liu DJ, Peloso GM, Zhan X, Holmen OL, Zawistowski M, Feng S, Nikpay M, Auer PL, Goel A, Zhang H, Peters U, Farrall M, Orho-Melander M, Kooperberg C, McPherson R, et al. Meta-analysis of gene-level tests for rare variant association. Nature Genetics. 46: 200-4. PMID 24336170 DOI: 10.1038/Ng.2852 |
0.478 |
|
| 2013 |
Schaibley VM, Zawistowski M, Wegmann D, Ehm MG, Nelson MR, St Jean PL, Abecasis GR, Novembre J, Zöllner S, Li JZ. The influence of genomic context on mutation patterns in the human genome inferred from rare variants. Genome Research. 23: 1974-84. PMID 23990608 DOI: 10.1101/Gr.154971.113 |
0.481 |
|
| 2013 |
Liu K, Fast S, Zawistowski M, Tintle NL. A geometric framework for evaluating rare variant tests of association. Genetic Epidemiology. 37: 345-57. PMID 23526307 DOI: 10.1002/Gepi.21722 |
0.448 |
|
| 2012 |
Nelson MR, Wegmann D, Ehm MG, Kessner D, St Jean P, Verzilli C, Shen J, Tang Z, Bacanu SA, Fraser D, Warren L, Aponte J, Zawistowski M, Liu X, Zhang H, et al. An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science (New York, N.Y.). 337: 100-4. PMID 22604722 DOI: 10.1126/Science.1217876 |
0.693 |
|
| 2012 |
Jewett EM, Zawistowski M, Rosenberg NA, Zöllner S. A coalescent model for genotype imputation. Genetics. 191: 1239-55. PMID 22595242 DOI: 10.1534/Genetics.111.137984 |
0.642 |
|
| 2010 |
Zawistowski M, Gopalakrishnan S, Ding J, Li Y, Grimm S, Zöllner S. Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes. American Journal of Human Genetics. 87: 604-17. PMID 21070896 DOI: 10.1016/J.Ajhg.2010.10.012 |
0.687 |
|
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