| Global patterns of linkage disequilibrium at the CD4 locus and modern human origins SA Tishkoff, E Dietzsch, W Speed, AJ Pakstis, JR Kidd, K Cheung, ... Science 271 (5254), 1380-1387, 1996 | 781 | 1996 |
| Mitochondrial footprints of human expansions in Africa E Watson, P Forster, M Richards, HJ Bandelt The American Journal of Human Genetics 61 (3), 691-704, 1997 | 496 | 1997 |
| Phylogeographic analysis of haplogroup E3b (E-M215) Y chromosomes reveals multiple migratory events within and out of Africa F Cruciani, R La Fratta, P Santolamazza, D Sellitto, R Pascone, P Moral, ... The American Journal of Human Genetics 74 (5), 1014-1022, 2004 | 290 | 2004 |
| Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12 F Cruciani, R La Fratta, B Trombetta, P Santolamazza, D Sellitto, ... Molecular biology and evolution 24 (6), 1300-1311, 2007 | 210 | 2007 |
| mtDNA sequence diversity in Africa. E Watson, K Bauer, R Aman, G Weiss, A von Haeseler, S Pääbo American Journal of Human Genetics 59 (2), 437, 1996 | 179 | 1996 |
| Human Y chromosome haplogroup R-V88: a paternal genetic record of early mid Holocene trans-Saharan connections and the spread of Chadic languages F Cruciani, B Trombetta, D Sellitto, A Massaia, G Destro-Bisol, E Watson, ... European Journal of Human Genetics 18 (7), 800-807, 2010 | 145 | 2010 |
| Guidelines for genetic testing and management of Alport syndrome J Savige, BS Lipska-Zietkiewicz, E Watson, JM Hertz, C Deltas, F Mari, ... Clinical Journal of the American Society of Nephrology 17 (1), 143-154, 2022 | 80 | 2022 |
| mtDNA mutation rates--no need to panic. VA Macaulay, MB Richards, P Forster, KE Bendall, E Watson, B Sykes, ... American journal of human genetics 61 (4), 983, 1997 | 72 | 1997 |
| Trees from languages and genes are very similar D Penny, EE Watson, MA Steel Systematic biology 42 (3), 382-384, 1993 | 48 | 1993 |
| The peopling of the last Green Sahara revealed by high-coverage resequencing of trans-Saharan patrilineages E D’Atanasio, B Trombetta, M Bonito, A Finocchio, G Di Vito, M Seghizzi, ... Genome biology 19, 1-15, 2018 | 42 | 2018 |
| Homo genus: a review of the classification of humans and the great apes EE Watson, D Penny, S Easteal Humanity from African naissance to coming millennia: colloquia in human …, 2001 | 34 | 2001 |
| Some recent progress with methods for evolutionary trees D Penny, EE Watson, RE Hickson, PJ Lockhart New Zealand Journal of Botany 31 (3), 275-288, 1993 | 32 | 1993 |
| An algorithm for constructing local regions in a phylogenetic network KT Huber, EE Watson, MD Hendy Molecular Phylogenetics and Evolution 19 (1), 1-8, 2001 | 16 | 2001 |
| Basement membrane defects in CD151-associated glomerular disease RW Naylor, E Watson, S Williamson, R Preston, JB Davenport, ... Pediatric Nephrology 37 (12), 3105-3115, 2022 | 9 | 2022 |
| Reply to Lancaster F Cruciani, B Trombetta, D Sellitto, A Massaia, G Destro-Bisol, E Watson, ... European Journal of Human Genetics 18 (11), 1186-1187, 2010 | 9 | 2010 |
| Threads from the past: a genetic study of African ethnic groups and human origins: a thesis presented in partial filfulment of the requirements for the degree of Doctor of … EE Watson Massey University, 1996 | 5 | 1996 |
| Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria J Savige, H Storey, E Watson, JM Hertz, C Deltas, A Renieri, F Mari, ... European Journal of Human Genetics 32 (1), 132-132, 2024 | 2 | 2024 |
| Ascertaining pathogenicity of genetic variants: caution required Z Arslan, E Watson, D Bockenhauer Pediatric Nephrology 38 (5), 1695-1696, 2023 | 1 | 2023 |
| The West Midland Familial Hypercholesterolaemia (FH) screening programme: Evaluating the utility of the 12 SNP polygenic risk score (PRS) across ethnic groupings E George, J Bellaby, S Day, R Dhillon, S Horton, K Dyer, R Cramb, ... Atherosclerosis Plus 43, S5-S6, 2021 | 1 | 2021 |
| Genetic testing for Familial Hypercholesterolaemia in the genomic era. The utility of an NGS test for monogenic and polygenic hypercholesterolaemia E Watson, J Honeychurch, A Hills, P Dean, L Yarram-Smith, G Woodward, ... Atherosclerosis Supplements 28, e4, 2017 | 1 | 2017 |
Fulvio CrucianiSapienza Università di Roma, Dipartimento di Biologia e Biotecnologie "Charles Darwin"在 uniroma1.it 的电子邮件经过验证
