| Year |
Citation |
Score |
| 2024 |
Voinescu CD, Mozere M, Genovese G, Downie ML, Gupta S, Gale DP, Bockenhauer D, Kleta R, Arcos-Burgos M, Stanescu HC. A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy. Kidney International. PMID 38367960 DOI: 10.1016/j.kint.2024.01.017 |
0.302 |
|
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Genovese G, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.32 |
|
| 2020 |
Loh PR, Genovese G, McCarroll SA. Monogenic and polygenic inheritance become instruments for clonal selection. Nature. PMID 32581363 DOI: 10.1038/S41586-020-2430-6 |
0.383 |
|
| 2020 |
Howrigan DP, Rose SA, Samocha KE, Fromer M, Cerrato F, Chen WJ, Churchhouse C, Chambert K, Chandler SD, Daly MJ, Dumont A, Genovese G, Hwu HG, Laird N, Kosmicki JA, et al. Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature Neuroscience. PMID 31932770 DOI: 10.1038/S41593-019-0564-3 |
0.395 |
|
| 2019 |
Thompson DJ, Genovese G, Halvardson J, Ulirsch JC, Wright DJ, Terao C, Davidsson OB, Day FR, Sulem P, Jiang Y, Danielsson M, Davies H, Dennis J, Dunlop MG, Easton DF, et al. Genetic predisposition to mosaic Y chromosome loss in blood. Nature. PMID 31748747 DOI: 10.1038/S41586-019-1765-3 |
0.387 |
|
| 2019 |
McGraw KL, Cheng CH, Chen YA, Hou HA, Nilsson B, Genovese G, Cluzeau T, Pellagatti A, Przychodzen BP, Mallo M, Arenillas L, Mohamedali A, Adès L, Sallman DA, Padron E, et al. Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis. Blood Advances. 3: 3579-3589. PMID 31738830 DOI: 10.1182/Bloodadvances.2019000922 |
0.371 |
|
| 2019 |
Terao C, Momozawa Y, Ishigaki K, Kawakami E, Akiyama M, Loh PR, Genovese G, Sugishita H, Ohta T, Hirata M, Perry JRB, Matsuda K, Murakami Y, Kubo M, Kamatani Y. GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation. Nature Communications. 10: 4719. PMID 31624269 DOI: 10.1038/S41467-019-12705-5 |
0.371 |
|
| 2019 |
Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Molecular Psychiatry. PMID 31591465 DOI: 10.1038/S41380-019-0517-Y |
0.41 |
|
| 2019 |
Wang M, Chun J, Genovese G, Knob AU, Benjamin A, Wilkins MS, Friedman DJ, Appel GB, Lifton RP, Mane S, Pollak MR. Contributions of Rare Gene Variants to Familial and Sporadic FSGS. Journal of the American Society of Nephrology : Jasn. PMID 31308072 DOI: 10.1681/Asn.2019020152 |
0.35 |
|
| 2019 |
Szatkiewicz J, Crowley JJ, Adolfsson AN, Åberg KA, Alaerts M, Genovese G, McCarroll S, Del-Favero J, Adolfsson R, Sullivan PF. The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. Translational Psychiatry. 9: 60. PMID 30718465 DOI: 10.1038/S41398-019-0414-9 |
0.383 |
|
| 2019 |
Bigdeli T, Aslan M, Genovese G, Iyegbe C, Charney A, Schooler N, Braff D, Muralidhar S, McCarroll S, Gaziano M, Pato M, Pato C, Harvey P, Fanous A. SHARED CONTRIBUTIONS OF COMMON GENETIC VARIANTS TO RISK OF PSYCHOSIS AMONG INDIVIDUALS OF AFRICAN, LATINO, AND EUROPEAN ANCESTRY European Neuropsychopharmacology. 29: S23-S24. DOI: 10.1016/J.Euroneuro.2019.07.047 |
0.371 |
|
| 2019 |
Peterson R, Bigdeli T, Meyers J, Genovese G, Pato M, McCarroll S, Pato C, Fanous A. SU119GENETIC OVERLAP AND CAUSALITY AMONG SCHIZOPHRENIA AND SUBSTANCE USE: FINDINGS FROM THE GENOMIC PSYCHIATRY COHORT European Neuropsychopharmacology. 29: S1330-S1331. DOI: 10.1016/J.Euroneuro.2018.08.483 |
0.338 |
|
| 2019 |
Bigdeli T, Genovese G, Medeiros H, Sobell J, Knowles J, Pato M, Fanous A, McCarroll S, Pato C. F118Contributions Of Common Genetic Variants To Schizophrenia Risk In Individuals With African And Latino Ancestry European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.198 |
0.383 |
|
| 2019 |
Iyegbe CO, Bidgeli T, Genovese G, Meyers J, Peterson R, Pato M, Pato C, Fanous A. F113MODELING COMMON VARIANT ATTRIBUTABLE RISK OF SCHIZOPHRENIA AND BIPOLAR DISORDER IN DIVERSE POPULATIONS European Neuropsychopharmacology. 29: S1171. DOI: 10.1016/J.Euroneuro.2018.08.193 |
0.346 |
|
| 2019 |
Crowley J, Mudgal P, Adolfsson AN, Åberg K, Alaerts M, Genovese G, McCarroll S, Del-Favero J, Adolfsson R, Sullivan P. The genomics of bipolar and schizophrenic disorders in a large pedigree from a northern Swedish isolate European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.217 |
0.314 |
|
| 2018 |
Ulirsch JC, Verboon JM, Kazerounian S, Guo MH, Yuan D, Ludwig LS, Handsaker RE, Abdulhay NJ, Fiorini C, Genovese G, Lim ET, Cheng A, Cummings BB, Chao KR, Beggs AH, et al. The Genetic Landscape of Diamond-Blackfan Anemia. American Journal of Human Genetics. PMID 30503522 DOI: 10.1016/J.Ajhg.2018.10.027 |
0.376 |
|
| 2018 |
Loh PR, Genovese G, Handsaker RE, Finucane HK, Reshef YA, Palamara PF, Birmann BM, Talkowski ME, Bakhoum SF, McCarroll SA, Price AL. Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations. Nature. PMID 29995854 DOI: 10.1038/S41586-018-0321-X |
0.367 |
|
| 2018 |
Martin AR, Karczewski KJ, Kerminen S, Kurki MI, Sarin AP, Artomov M, Eriksson JG, Esko T, Genovese G, Havulinna AS, Kaprio J, Konradi A, Korányi L, Kostareva A, Männikkö M, et al. Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland. American Journal of Human Genetics. PMID 29706349 DOI: 10.1016/J.Ajhg.2018.03.003 |
0.359 |
|
| 2018 |
Finucane HK, Reshef YA, Anttila V, Slowikowski K, Gusev A, Byrnes A, Gazal S, Loh PR, Lareau C, Shoresh N, Genovese G, Saunders A, Macosko E, Pollack S, et al. Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. Nature Genetics. 50: 621-629. PMID 29632380 DOI: 10.1038/S41588-018-0081-4 |
0.354 |
|
| 2018 |
Zhang JY, Wang M, Tian L, Genovese G, Yan P, Wilson JG, Thadhani R, Mottl AK, Appel GB, Bick AG, Sampson MG, Alper SL, Friedman DJ, Pollak MR.
modifies-induced kidney disease risk. Proceedings of the National Academy of Sciences of the United States of America. PMID 29531077 DOI: 10.1073/Pnas.1716113115 |
0.345 |
|
| 2018 |
Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry. 23: 162-163. PMID 29296025 DOI: 10.1038/Mp.2017.214 |
0.355 |
|
| 2017 |
Artomov M, Rivas MA, Genovese G, Daly MJ. Mosaic mutations in blood DNA sequence are associated with solid tumor cancers. Npj Genomic Medicine. 2: 22. PMID 29263833 DOI: 10.1038/S41525-017-0025-4 |
0.302 |
|
| 2017 |
Nguyen HT, Bryois J, Kim A, Dobbyn A, Huckins LM, Munoz-Manchado AB, Ruderfer DM, Genovese G, Fromer M, Xu X, Pinto D, Linnarsson S, Verhage M, Smit AB, Hjerling-Leffler J, et al. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders. Genome Medicine. 9: 114. PMID 29262854 DOI: 10.1186/S13073-017-0497-Y |
0.371 |
|
| 2017 |
Merkle FT, Ghosh S, Kamitaki N, Mitchell J, Avior Y, Mello C, Kashin S, Mekhoubad S, Ilic D, Charlton M, Saphier G, Handsaker RE, Genovese G, Bar S, Benvenisty N, et al. Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations. Nature. PMID 28445466 DOI: 10.1038/Nature22312 |
0.316 |
|
| 2017 |
Genovese G, Fromer M, Stahl E, Ruderfer D, Chambert K, Landen M, Moran J, Purcell S, Sklar P, Sullivan P, Hultman C, McCarroll S. Ultra-Rare Protein-Altering Variants Among 4,877 Swedish Individuals with Schizophrenia European Neuropsychopharmacology. 27: S426-S427. DOI: 10.1016/J.Euroneuro.2016.09.480 |
0.326 |
|
| 2016 |
Johnson EC, Bjelland DW, Howrigan DP, Abdellaoui A, Breen G, Borglum A, Cichon S, Degenhardt F, Forstner AJ, Frank J, Genovese G, Heilmann-Heimbach S, Herms S, Hoffman P, Maier W, et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. Plos Genetics. 12: e1006343. PMID 27792727 DOI: 10.1371/Journal.Pgen.1006343 |
0.367 |
|
| 2016 |
Genovese G, Fromer M, Stahl EA, Ruderfer DM, Chambert K, Landén M, Moran JL, Purcell SM, Sklar P, Sullivan PF, Hultman CM, McCarroll SA. Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia. Nature Neuroscience. PMID 27694994 DOI: 10.1038/Nn.4402 |
0.388 |
|
| 2016 |
Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki MI, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, et al. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nature Neuroscience. PMID 27694993 DOI: 10.1038/Nn.4404 |
0.355 |
|
| 2016 |
Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry. PMID 27400856 DOI: 10.1038/Mp.2016.97 |
0.435 |
|
| 2016 |
Sekar A, Bialas AR, de Rivera H, Davis A, Hammond TR, Kamitaki N, Tooley K, Presumey J, Baum M, Van Doren V, Genovese G, Rose SA, Handsaker RE, Daly MJ, et al. Schizophrenia risk from complex variation of complement component 4. Nature. PMID 26814963 DOI: 10.1038/Nature16549 |
0.348 |
|
| 2016 |
McGraw K, Cheng C, Chen A, Genovese G, Cluzeau T, Lin H, Przychodzen B, Mallo M, Arenillas L, Mohamedali A, Ades L, Basiorka A, Irvine B, Sallman D, Padron E, et al. Abstract 2570: Identification of genetic polymorphisms associated with myelodysplastic syndromes by genome-wide association study Cancer Research. 76: 2570-2570. DOI: 10.1158/1538-7445.Am2016-2570 |
0.406 |
|
| 2015 |
Palamara PF, Francioli LC, Wilton PR, Genovese G, Gusev A, Finucane HK, Sankararaman S, Sunyaev SR, de Bakker PI, Wakeley J, Pe'er I, Price AL. Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates. American Journal of Human Genetics. PMID 26581902 DOI: 10.1016/J.Ajhg.2015.10.006 |
0.352 |
|
| 2015 |
Vilhjálmsson BJ, Yang J, Finucane HK, Gusev A, Lindström S, Ripke S, Genovese G, Loh PR, Bhatia G, Do R, Hayeck T, Won HH, Kathiresan S, et al. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. American Journal of Human Genetics. 97: 576-592. PMID 26430803 DOI: 10.1016/J.Ajhg.2015.09.001 |
0.322 |
|
| 2015 |
Hawkins GA, Friedman DJ, Lu L, McWilliams DR, Chou JW, Sajuthi S, Divers J, Parekh RS, Li M, Genovese G, Pollack MR, Hicks PJ, Bowden DW, Ma L, Freedman BI, et al. Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression. American Journal of Nephrology. 42: 99-106. PMID 26343748 DOI: 10.1159/000439448 |
0.372 |
|
| 2015 |
Ruchi R, Genovese G, Lee J, Charoonratana VT, Bernhardy AJ, Alper SL, Kopp JB, Thadhani R, Friedman DJ, Pollak MR. Copy Number Variation at the APOL1 Locus. Plos One. 10: e0125410. PMID 25933006 DOI: 10.1371/Journal.Pone.0125410 |
0.419 |
|
| 2015 |
Williams AL, Genovese G, Dyer T, Altemose N, Truax K, Jun G, Patterson N, Myers SR, Curran JE, Duggirala R, Blangero J, Reich D, Przeworski M. Non-crossover gene conversions show strong GC bias and unexpected clustering in humans. Elife. 4. PMID 25806687 DOI: 10.7554/Elife.04637 |
0.351 |
|
| 2015 |
Handsaker RE, Van Doren V, Berman JR, Genovese G, Kashin S, Boettger LM, McCarroll SA. Large multiallelic copy number variations in humans. Nature Genetics. 47: 296-303. PMID 25621458 DOI: 10.1038/Ng.3200 |
0.409 |
|
| 2015 |
Green EK, Rees E, Walters JT, Smith KG, Forty L, Grozeva D, Moran JL, Sklar P, Ripke S, Chambert KD, Genovese G, McCarroll SA, Jones I, Jones L, Owen MJ, et al. Copy number variation in bipolar disorder. Molecular Psychiatry. PMID 25560756 DOI: 10.1038/Mp.2014.174 |
0.322 |
|
| 2015 |
Ruderfer DM, Lim ET, Genovese G, Moran JL, Hultman CM, Sullivan PF, McCarroll SA, Holmans P, Sklar P, Purcell SM. No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia. European Journal of Human Genetics : Ejhg. 23: 555-7. PMID 25370044 DOI: 10.1038/Ejhg.2014.228 |
0.447 |
|
| 2014 |
Thomson R, Genovese G, Canon C, Kovacsics D, Higgins MK, Carrington M, Winkler CA, Kopp J, Rotimi C, Adeyemo A, Doumatey A, Ayodo G, Alper SL, Pollak MR, Friedman DJ, et al. Evolution of the primate trypanolytic factor APOL1. Proceedings of the National Academy of Sciences of the United States of America. 111: E2130-9. PMID 24808134 DOI: 10.1073/Pnas.1400699111 |
0.366 |
|
| 2014 |
Barua M, Stellacci E, Stella L, Weins A, Genovese G, Muto V, Caputo V, Toka HR, Charoonratana VT, Tartaglia M, Pollak MR. Mutations in PAX2 associate with adult-onset FSGS. Journal of the American Society of Nephrology : Jasn. 25: 1942-53. PMID 24676634 DOI: 10.1681/Asn.2013070686 |
0.353 |
|
| 2014 |
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O'Dushlaine C, Chambert K, Bergen SE, Kähler A, Duncan L, Stahl E, Genovese G, Fernández E, Collins MO, et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 506: 185-90. PMID 24463508 DOI: 10.1038/Nature12975 |
0.439 |
|
| 2014 |
Ito K, Bick AG, Flannick J, Friedman DJ, Genovese G, Parfenov MG, Depalma SR, Gupta N, Gabriel SB, Taylor HA, Fox ER, Newton-Cheh C, Kathiresan S, Hirschhorn JN, Altshuler DM, et al. Increased burden of cardiovascular disease in carriers of APOL1 genetic variants. Circulation Research. 114: 845-50. PMID 24379297 DOI: 10.1161/Circresaha.114.302347 |
0.358 |
|
| 2014 |
Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, ... ... Genovese G, et al. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry. 19: 37-40. PMID 24217254 DOI: 10.1038/Mp.2013.156 |
0.361 |
|
| 2014 |
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics. 23: 1669-76. PMID 24163246 DOI: 10.1093/Hmg/Ddt540 |
0.394 |
|
| 2014 |
Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis. Kidney International. 85: 124-33. PMID 24048372 DOI: 10.1038/Ki.2013.354 |
0.372 |
|
| 2013 |
Toka HR, Genovese G, Mount DB, Pollak MR, Curhan GC. Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretion. Plos One. 8: e71885. PMID 23991001 DOI: 10.1371/Journal.Pone.0071885 |
0.328 |
|
| 2013 |
Genovese G, Handsaker RE, Li H, Kenny EE, McCarroll SA. Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes. American Journal of Human Genetics. 93: 411-21. PMID 23932108 DOI: 10.1016/J.Ajhg.2013.07.002 |
0.335 |
|
| 2013 |
Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nature Reviews. Nephrology. 9: 240-4. PMID 23438974 DOI: 10.1038/Nrneph.2013.34 |
0.408 |
|
| 2013 |
Genovese G, Handsaker RE, Li H, Altemose N, Lindgren AM, Chambert K, Pasaniuc B, Price AL, Reich D, Morton CC, Pollak MR, Wilson JG, McCarroll SA. Using population admixture to help complete maps of the human genome. Nature Genetics. 45: 406-14, 414e1-2. PMID 23435088 DOI: 10.1038/Ng.2565 |
0.369 |
|
| 2013 |
Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney International. 83: 316-22. PMID 23014460 DOI: 10.1038/Ki.2012.349 |
0.339 |
|
| 2012 |
Zaitlen N, Lindström S, Pasaniuc B, Cornelis M, Genovese G, Pollack S, Barton A, Bickeböller H, Bowden DW, Eyre S, Freedman BI, Friedman DJ, Field JK, Groop L, Haugen A, et al. Informed conditioning on clinical covariates increases power in case-control association studies. Plos Genetics. 8: e1003032. PMID 23144628 DOI: 10.1371/Journal.Pgen.1003032 |
0.317 |
|
| 2012 |
Pollak MR, Genovese G, Friedman DJ. APOL1 and kidney disease. Current Opinion in Nephrology and Hypertension. 21: 179-82. PMID 22257798 DOI: 10.1097/Mnh.0B013E32835012Ab |
0.327 |
|
| 2011 |
Kanji Z, Powe CE, Wenger JB, Huang C, Ankers E, Sullivan DA, Collerone G, Powe NR, Tonelli M, Bhan I, Bernhardy AJ, Dibartolo S, Friedman D, Genovese G, Pollak MR, et al. Genetic variation in APOL1 associates with younger age at hemodialysis initiation. Journal of the American Society of Nephrology : Jasn. 22: 2091-7. PMID 21997398 DOI: 10.1681/Asn.2010121234 |
0.352 |
|
| 2011 |
Friedman DJ, Kozlitina J, Genovese G, Jog P, Pollak MR. Population-based risk assessment of APOL1 on renal disease. Journal of the American Society of Nephrology : Jasn. 22: 2098-105. PMID 21997396 DOI: 10.1681/Asn.2011050519 |
0.339 |
|
| 2011 |
Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, Friedman D, Briggs W, Dart R, Korbet S, Mokrzycki MH, Kimmel PL, Limou S, Ahuja TS, Berns JS, et al. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. Journal of the American Society of Nephrology : Jasn. 22: 2129-37. PMID 21997394 DOI: 10.1681/Asn.2011040388 |
0.383 |
|
| 2011 |
Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, Mallick S, Myers S, Tandon A, Spencer C, Palmer CD, Adeyemo AA, Akylbekova EL, Cupples LA, Divers J, et al. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. American Journal of Human Genetics. 89: 368-81. PMID 21907010 DOI: 10.1016/J.Ajhg.2011.07.025 |
0.354 |
|
| 2011 |
Al-Romaih KI, Genovese G, Al-Mojalli H, Al-Othman S, Al-Manea H, Al-Suleiman M, Al-Jondubi M, Atallah N, Al-Rodayyan M, Weins A, Pollak MR, Adra CN. Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencing. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 58: 186-95. PMID 21658830 DOI: 10.1053/J.Ajkd.2011.01.025 |
0.32 |
|
| 2010 |
Freedman BI, Kopp JB, Langefeld CD, Genovese G, Friedman DJ, Nelson GW, Winkler CA, Bowden DW, Pollak MR. The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans. Journal of the American Society of Nephrology : Jasn. 21: 1422-6. PMID 20688934 DOI: 10.1681/Asn.2010070730 |
0.44 |
|
| 2010 |
Genovese G, Tonna SJ, Knob AU, Appel GB, Katz A, Bernhardy AJ, Needham AW, Lazarus R, Pollak MR. A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. Kidney International. 78: 698-704. PMID 20668430 DOI: 10.1038/Ki.2010.251 |
0.407 |
|
| 2010 |
Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, et al. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science (New York, N.Y.). 329: 841-5. PMID 20647424 DOI: 10.1126/Science.1193032 |
0.341 |
|
| 2010 |
Genovese G, Leibon G, Pollak MR, Rockmore DN. Improved IBD detection using incomplete haplotype information. Bmc Genetics. 11: 58. PMID 20591167 DOI: 10.1186/1471-2156-11-58 |
0.6 |
|
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