| Year |
Citation |
Score |
| 2024 |
Lippincott MF, Schafer EC, Hindman AA, He W, Brauner R, Delaney A, Grinspon R, Hall JE, Hirschhorn JN, McElreavey K, Palmert MR, Rey R, Seminara SB, Salem RM, Chan YM. Contributions of common genetic variants to constitutional delay of puberty and idiopathic hypogonadotropic hypogonadism. The Journal of Clinical Endocrinology and Metabolism. PMID 38477512 DOI: 10.1210/clinem/dgae166 |
0.547 |
|
| 2024 |
Lawrence ES, Gu W, Bohlender RJ, Anza-Ramirez C, Cole AM, Yu JJ, Hu H, Heinrich EC, O'Brien KA, Vasquez CA, Cowan QT, Bruck PT, Mercader K, Alotaibi M, Long T, ... ... Salem RM, et al. Functional / missense variant is associated with hematocrit in Andean highlanders. Science Advances. 10: eadj5661. PMID 38335297 DOI: 10.1126/sciadv.adj5661 |
0.347 |
|
| 2023 |
Zhu J, Eliasen AU, Aris IM, Stinson SE, Holm JC, Hansen T, Hivert MF, Bønnelykke K, Salem RM, Hirschhorn JN, Chan YM. Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome. The Journal of Clinical Endocrinology and Metabolism. PMID 37690116 DOI: 10.1210/clinem/dgad533 |
0.401 |
|
| 2023 |
Bartell E, Lin K, Tsuo K, Gan W, Vedantam S, Cole JB, Baronas JM, Yengo L, Marouli E, Amariuta T, Chen Z, Li L, Renthal NE, Jacobsen CM, Salem RM, et al. Genetics of skeletal proportions in two different populations. Biorxiv : the Preprint Server For Biology. PMID 37292977 DOI: 10.1101/2023.05.22.541772 |
0.744 |
|
| 2023 |
Hill C, Duffy S, Kettyle LM, McGlynn L, Sandholm N, Salem RM, Thompson A, Swan EJ, Kilner J, Rossing P, Shiels PG, Lajer M, Groop PH, Maxwell AP, McKnight AJ. Differential Methylation of Telomere-Related Genes Is Associated with Kidney Disease in Individuals with Type 1 Diabetes. Genes. 14. PMID 37239390 DOI: 10.3390/genes14051029 |
0.335 |
|
| 2022 |
Smyth LJ, Dahlström EH, Syreeni A, Kerr K, Kilner J, Doyle R, Brennan E, Nair V, Fermin D, Nelson RG, Looker HC, Wooster C, Andrews D, Anderson K, McKay GJ, ... ... Salem RM, et al. Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease. Nature Communications. 13: 7891. PMID 36550108 DOI: 10.1038/s41467-022-34963-6 |
0.46 |
|
| 2022 |
Maihofer AX, Engchuan W, Huguet G, Klein M, MacDonald JR, Shanta O, Thiruvahindrapuram B, Jean-Louis M, Saci Z, Jacquemont S, Scherer SW, Ketema E, Aiello AE, Amstadter AB, Avdibegović E, ... ... Salem RM, et al. Rare copy number variation in posttraumatic stress disorder. Molecular Psychiatry. PMID 36131047 DOI: 10.1038/s41380-022-01776-4 |
0.307 |
|
| 2022 |
Sandholm N, Cole JB, Nair V, Sheng X, Liu H, Ahlqvist E, van Zuydam N, Dahlström EH, Fermin D, Smyth LJ, Salem RM, Forsblom C, Valo E, Harjutsalo V, Brennan EP, et al. Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Diabetologia. PMID 35763030 DOI: 10.1007/s00125-022-05735-0 |
0.565 |
|
| 2021 |
Wang H, Lo MT, Rosenthal SB, Makowski C, Andreassen OA, Salem RM, McEvoy LK, Fiecas M, Chen CH. Similar Genetic Architecture of Alzheimer's Disease and Differential Effect Between Sexes. Frontiers in Aging Neuroscience. 13: 674318. PMID 34122051 DOI: 10.3389/fnagi.2021.674318 |
0.314 |
|
| 2021 |
Thaker VV, Deng S, Gorski G, Vedantam S, Clish C, Salem R, Hirschhorn JN. Baseline Metabolomic Profile as Potential Biomarker for Weight Change After Roux-en-Y Gastric Bypass Surgery Journal of the Endocrine Society. 5: A5-A5. DOI: 10.1210/jendso/bvab048.009 |
0.639 |
|
| 2019 |
Geidenstam N, Hsu YH, Astley CM, Mercader JM, Ridderstråle M, Gonzalez ME, Gonzalez C, Hirschhorn JN, Salem RM. Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Plos One. 14: e0222445. PMID 31560688 DOI: 10.1371/Journal.Pone.0222445 |
0.71 |
|
| 2019 |
Salem RM, Todd JN, Sandholm N, Cole JB, Chen WM, Andrews D, Pezzolesi MG, McKeigue PM, Hiraki LT, Qiu C, Nair V, Di Liao C, Cao JJ, Valo E, Onengut-Gumuscu S, et al. Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Journal of the American Society of Nephrology : Jasn. PMID 31537649 DOI: 10.1681/Asn.2019030218 |
0.527 |
|
| 2019 |
Ulirsch JC, Lareau CA, Bao EL, Ludwig LS, Guo MH, Benner C, Satpathy AT, Kartha VK, Salem RM, Hirschhorn JN, Finucane HK, Aryee MJ, Buenrostro JD, Sankaran VG. Interrogation of human hematopoiesis at single-cell and single-variant resolution. Nature Genetics. PMID 30858613 DOI: 10.1038/S41588-019-0362-6 |
0.74 |
|
| 2018 |
van Zuydam NR, Ahlqvist E, Sandholm N, Deshmukh H, Rayner NW, Abdalla M, Ladenvall C, Ziemek D, Fauman E, Robertson NR, McKeigue PM, Valo E, Forsblom C, Harjutsalo V, ... ... Salem RM, et al. A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Diabetes. PMID 29703844 DOI: 10.2337/Db17-0914 |
0.528 |
|
| 2018 |
Astley CM, Todd JN, Salem RM, Vedantam S, Ebbeling CB, Huang PL, Ludwig DS, Hirschhorn JN, Florez JC. Genetic Evidence That Carbohydrate-Stimulated Insulin Secretion Leads to Obesity. Clinical Chemistry. 64: 192-200. PMID 29295838 DOI: 10.1373/Clinchem.2017.280727 |
0.43 |
|
| 2018 |
Bao EL, Ulirsch JC, Lareau CA, Ludwig LS, Guo MH, Benner C, Satpathy AT, Kartha VK, Salem RM, Hirschhorn JN, Finucane HK, Aryee MJ, Buenrostro JD, Sankaran VG. Dissecting the Regulation of Human Hematopoiesis at Single-Cell and Single-Variant Resolution Blood. 132: 531-531. DOI: 10.1182/Blood-2018-99-112624 |
0.728 |
|
| 2016 |
Guo MH, Nandakumar SK, Ulirsch JC, Zekavat SM, Buenrostro JD, Natarajan P, Salem RM, Chiarle R, Mitt M, Kals M, Pärn K, Fischer K, Milani L, Mägi R, Palta P, et al. Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Proceedings of the National Academy of Sciences of the United States of America. PMID 28031487 DOI: 10.1073/Pnas.1619052114 |
0.729 |
|
| 2016 |
Sandholm N, Van Zuydam N, Ahlqvist E, Juliusdottir T, Deshmukh HA, Rayner NW, Di Camillo B, Forsblom C, Fadista J, Ziemek D, Salem RM, Hiraki LT, Pezzolesi M, Trégouët D, Dahlström E, et al. The Genetic Landscape of Renal Complications in Type 1 Diabetes. Journal of the American Society of Nephrology : Jasn. PMID 27647854 DOI: 10.1681/Asn.2016020231 |
0.532 |
|
| 2016 |
Guo MH, Dauber A, Lippincott MF, Chan YM, Salem RM, Hirschhorn JN. Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders. American Journal of Human Genetics. PMID 27545677 DOI: 10.1016/J.Ajhg.2016.06.031 |
0.724 |
|
| 2016 |
Boettger LM, Salem RM, Handsaker RE, Peloso GM, Kathiresan S, Hirschhorn JN, McCarroll SA. Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels. Nature Genetics. PMID 26901066 DOI: 10.1038/Ng.3510 |
0.51 |
|
| 2016 |
Todd JN, Salem R, Sandholm N, Valo EA, Hiraki LT, Liao CD, Pezzolesi MG, Smiles A, Onengut-Gumuscu S, Chen WM, McGurnaghan S, McKeigue P, McKnight AJ, Maxwell AP, Colhoun HM, et al. Novel Genetic Determinants of Diabetic Kidney Disease Diabetes. 65. DOI: 10.2337/Db16-1-381 |
0.555 |
|
| 2015 |
Giani FC, Fiorini C, Wakabayashi A, Ludwig LS, Salem RM, Jobaliya CD, Regan SN, Ulirsch JC, Liang G, Steinberg-Shemer O, Guo MH, Esko T, Tong W, Brugnara C, Hirschhorn JN, et al. Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells. Cell Stem Cell. PMID 26607381 DOI: 10.1016/J.Stem.2015.09.015 |
0.666 |
|
| 2015 |
Todd JN, Dahlström EH, Salem RM, Sandholm N, Forsblom C, McKnight AJ, Maxwell AP, Brennan E, Sadlier D, Godson C, Groop PH, Hirschhorn JN, Florez JC. Genetic Evidence for a Causal Role of Obesity in Diabetic Kidney Disease. Diabetes. PMID 26307587 DOI: 10.2337/Db15-0254 |
0.505 |
|
| 2015 |
Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, ... ... Salem RM, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 523: 459-62. PMID 26131930 DOI: 10.1038/Nature14618 |
0.557 |
|
| 2015 |
Chan Y, Salem RM, Hsu YH, McMahon G, Pers TH, Vedantam S, Esko T, Guo MH, Lim ET, Franke L, Smith GD, Strachan DP, Hirschhorn JN. Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. American Journal of Human Genetics. 96: 695-708. PMID 25865494 DOI: 10.1016/J.Ajhg.2015.02.018 |
0.755 |
|
| 2015 |
Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S, Buchkovich ML, Yang J, Croteau-Chonka DC, Esko T, Fall T, Ferreira T, Gustafsson S, ... ... Salem RM, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 518: 197-206. PMID 25673413 DOI: 10.1038/Nature14177 |
0.507 |
|
| 2015 |
Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE, Workalemahu T, Wu JM, Buchkovich ML, Heard-Costa NL, Roman TS, ... ... Salem RM, et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 518: 187-96. PMID 25673412 DOI: 10.1038/Nature14132 |
0.554 |
|
| 2014 |
Lim ET, Würtz P, Havulinna AS, Palta P, Tukiainen T, Rehnström K, Esko T, Mägi R, Inouye M, Lappalainen T, Chan Y, Salem RM, Lek M, Flannick J, Sim X, et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. Plos Genetics. 10: e1004494. PMID 25078778 DOI: 10.1371/Journal.Pgen.1004494 |
0.554 |
|
| 2014 |
Chan Y, Lim ET, Sandholm N, Wang SR, McKnight AJ, Ripke S, Daly MJ, Neale BM, Salem RM, Hirschhorn JN. An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases. American Journal of Human Genetics. 94: 437-52. PMID 24607388 DOI: 10.1016/J.Ajhg.2014.02.006 |
0.535 |
|
| 2013 |
Sandholm N, McKnight AJ, Salem RM, Brennan EP, Forsblom C, Harjutsalo V, Mäkinen VP, McKay GJ, Sadlier DM, Williams WW, Martin F, Panduru NM, Tarnow L, Tuomilehto J, Tryggvason K, et al. Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes. Journal of the American Society of Nephrology : Jasn. 24: 1537-43. PMID 24029427 DOI: 10.1681/Asn.2012111122 |
0.527 |
|
| 2013 |
Horikoshi M, Yaghootkar H, Mook-Kanamori DO, Sovio U, Taal HR, Hennig BJ, Bradfield JP, St Pourcain B, Evans DM, Charoen P, Kaakinen M, Cousminer DL, Lehtimäki T, Kreiner-Møller E, Warrington NM, ... ... Salem RM, et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nature Genetics. 45: 76-82. PMID 23202124 DOI: 10.1038/Ng.2477 |
0.583 |
|
| 2012 |
Sandholm N, Salem RM, McKnight AJ, Brennan EP, Forsblom C, Isakova T, McKay GJ, Williams WW, Sadlier DM, Mäkinen VP, Swan EJ, Palmer C, Boright AP, Ahlqvist E, Deshmukh HA, et al. New susceptibility loci associated with kidney disease in type 1 diabetes. Plos Genetics. 8: e1002921. PMID 23028342 DOI: 10.1371/Journal.Pgen.1002921 |
0.551 |
|
| 2012 |
Williams WW, Salem RM, McKnight AJ, Sandholm N, Forsblom C, Taylor A, Guiducci C, McAteer JB, McKay GJ, Isakova T, Brennan EP, Sadlier DM, Palmer C, Söderlund J, Fagerholm E, et al. Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy. Diabetes. 61: 2187-94. PMID 22721967 DOI: 10.2337/Db11-0751 |
0.554 |
|
| 2012 |
Bradfield JP, Taal HR, Timpson NJ, Scherag A, Lecoeur C, Warrington NM, Hypponen E, Holst C, Valcarcel B, Thiering E, Salem RM, Schumacher FR, Cousminer DL, Sleiman PM, Zhao J, et al. A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics. 44: 526-31. PMID 22484627 DOI: 10.1038/Ng.2247 |
0.579 |
|
| 2010 |
Chen Y, Rao F, Wen G, Gayen JR, Zhang K, Vaingankar SM, Biswas N, Mahata M, Friese RS, Fung MM, Salem RM, Nievergelt C, Bhatnagar V, Hook VY, Ziegler MG, et al. Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease. Cellular and Molecular Neurobiology. 30: 1395-400. PMID 21061160 DOI: 10.1007/S10571-010-9600-2 |
0.314 |
|
| 2010 |
Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, ... ... Salem RM, et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 467: 832-8. PMID 20881960 DOI: 10.1038/Nature09410 |
0.64 |
|
| 2010 |
Smith EN, Chen W, Kähönen M, Kettunen J, Lehtimäki T, Peltonen L, Raitakari OT, Salem RM, Schork NJ, Shaw M, Srinivasan SR, Topol EJ, Viikari JS, Berenson GS, Murray SS. Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. Plos Genetics. 6: e1001094. PMID 20838585 DOI: 10.1371/journal.pgen.1001094 |
0.371 |
|
| 2010 |
Salem RM, O'Connor DT, Schork NJ. Curve-based multivariate distance matrix regression analysis: application to genetic association analyses involving repeated measures. Physiological Genomics. 42: 236-47. PMID 20423962 DOI: 10.1152/physiolgenomics.00118.2009 |
0.329 |
|
| 2008 |
Chen Y, Rao F, Rodriguez-Flores JL, Mahata M, Fung MM, Stridsberg M, Vaingankar SM, Wen G, Salem RM, Das M, Cockburn MG, Schork NJ, Ziegler MG, Hamilton BA, Mahata SK, et al. Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion. Journal of the American College of Cardiology. 52: 1468-81. PMID 19017515 DOI: 10.1016/j.jacc.2008.07.047 |
0.306 |
|
| 2008 |
Fung MM, Nguyen C, Mehtani P, Salem RM, Perez B, Thomas B, Das M, Schork NJ, Mahata SK, Ziegler MG, O'Connor DT. Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans. Circulation. 117: 517-25. PMID 18180394 DOI: 10.1161/CIRCULATIONAHA.107.706317 |
0.307 |
|
| 2007 |
Zhang L, Rao F, Zhang K, Khandrika S, Das M, Vaingankar SM, Bao X, Rana BK, Smith DW, Wessel J, Salem RM, Rodriguez-Flores JL, Mahata SK, Schork NJ, Ziegler MG, et al. Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular risk. The Journal of Clinical Investigation. 117: 2658-71. PMID 17717598 DOI: 10.1172/JCI31093 |
0.303 |
|
| 2004 |
McCarthy JJ, Parker A, Salem R, Moliterno DJ, Wang QK, Plow EF, Rao S, Shen G, Rogers WJ, Newby LK, Cannata R, Glatt K, Topol EJ. Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes Journal of Medical Genetics. 41: 334-341. PMID 15121769 DOI: 10.1136/Jmg.2003.016584 |
0.424 |
|
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