| Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene S Tzur, S Rosset, R Shemer, G Yudkovsky, S Selig, A Tarekegn, E Bekele, ... Human genetics 128, 345-350, 2010 | 639 | 2010 |
| The dawn of human matrilineal diversity DM Behar, R Villems, H Soodyall, J Blue-Smith, L Pereira, E Metspalu, ... The American Journal of Human Genetics 82 (5), 1130-1140, 2008 | 603 | 2008 |
| Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter–gatherers and Bantu-speaking farmers L Quintana-Murci, H Quach, C Harmant, F Luca, B Massonnet, E Patin, ... Proceedings of the National Academy of Sciences 105 (5), 1596-1601, 2008 | 235 | 2008 |
| The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event DM Behar, E Metspalu, T Kivisild, A Achilli, Y Hadid, S Tzur, L Pereira, ... The American Journal of Human Genetics 78 (3), 487-497, 2006 | 228 | 2006 |
| Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora DM Behar, E Metspalu, T Kivisild, S Rosset, S Tzur, Y Hadid, G Yudkovsky, ... Plos one 3 (4), e2062, 2008 | 177 | 2008 |
| The Genographic Project public participation mitochondrial DNA database DM Behar, S Rosset, J Blue-Smith, O Balanovsky, S Tzur, D Comas, ... PLoS Genetics 3 (6), e104, 2007 | 172 | 2007 |
| The Genographic Project public participation mitochondrial DNA database DM Behar, S Rosset, J Blue-Smith, O Balanovsky, S Tzur, D Comas, ... PLoS Genetics 3 (6), e104, 2007 | 172 | 2007 |
| Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency L de Vries, DM Behar, P Smirin-Yosef, I Lagovsky, S Tzur, ... The Journal of Clinical Endocrinology & Metabolism 99 (10), E2129-E2132, 2014 | 159 | 2014 |
| APOL1 risk variants predict histopathology and progression to ESRD in HIV-related kidney disease DM Fine, WG Wasser, MM Estrella, MG Atta, M Kuperman, R Shemer, ... Journal of the American Society of Nephrology 23 (2), 343-350, 2012 | 136 | 2012 |
| No evidence from genome-wide data of a Khazar origin for the Ashkenazi Jews DM Behar, M Metspalu, Y Baran, NM Kopelman, B Yunusbayev, ... Human biology 85 (6), 859-900, 2013 | 118 | 2013 |
| High population frequencies of APOL1 risk variants are associated with increased prevalence of non-diabetic chronic kidney disease in the Igbo people from south-eastern Nigeria II Ulasi, S Tzur, WG Wasser, R Shemer, E Kruzel, E Feigin, CK Ijoma, ... Nephron Clinical Practice 123 (1-2), 123-128, 2013 | 112 | 2013 |
| African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans DM Behar, S Rosset, S Tzur, S Selig, G Yudkovsky, S Bercovici, JB Kopp, ... Human molecular genetics 19 (9), 1816-1827, 2010 | 105 | 2010 |
| APOL1 allelic variants are associated with lower age of dialysis initiation and thereby increased dialysis vintage in African and Hispanic Americans with non-diabetic end-stage … S Tzur, S Rosset, K Skorecki, WG Wasser Nephrology Dialysis Transplantation 27 (4), 1498-1505, 2012 | 101 | 2012 |
| Deficiency of the sphingosine‐1‐phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications AR Janecke, R Xu, E Steichen‐Gersdorf, S Waldegger, A Entenmann, ... Human Mutation 38 (4), 365-372, 2017 | 92 | 2017 |
| Absence of APOL1 risk variants protects against HIV-associated nephropathy in the Ethiopian population DM Behar, E Kedem, S Rosset, Y Haileselassie, S Tzur, Z Kra-Oz, ... American journal of nephrology 34 (5), 452-459, 2011 | 91 | 2011 |
| The population genetics of chronic kidney disease: insights from the MYH9–APOL1 locus S Rosset, S Tzur, DM Behar, WG Wasser, K Skorecki Nature Reviews Nephrology 7 (6), 313-326, 2011 | 85 | 2011 |
| Gain-of-function mutation of microRNA-140 in human skeletal dysplasia G Grigelioniene, HI Suzuki, F Taylan, F Mirzamohammadi, ... Nature medicine 25 (4), 583-590, 2019 | 83 | 2019 |
| Possible incipient sympatric ecological speciation in blind mole rats (Spalax) Y Hadid, S Tzur, T Pavlíček, R Šumbera, J Šklíba, M Lövy, ... Proceedings of the National Academy of Sciences 110 (7), 2587-2592, 2013 | 72 | 2013 |
| Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5 D Magen, A Ofir, L Berger, D Goldsher, A Eran, N Katib, Y Nijem, ... Human genetics 134, 305-314, 2015 | 71 | 2015 |
| Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi Levites S Rootsi, DM Behar, M Järve, AA Lin, NM Myres, B Passarelli, GD Poznik, ... Nature communications 4 (1), 2928, 2013 | 70 | 2013 |
Karl SkoreckiAzrieli Faculty of Medicine, Bar-Ilan UniversityVerified email at biu.ac.il
