| GJB2 mutations and degree of hearing loss: a multicenter study RL Snoeckx, PLM Huygen, D Feldmann, S Marlin, F Denoyelle, ... The American Journal of Human Genetics 77 (6), 945-957, 2005 | 673 | 2005 |
| Correlation between genetic and geographic structure in Europe O Lao, TT Lu, M Nothnagel, O Junge, S Freitag-Wolf, A Caliebe, ... Current Biology 18 (16), 1241-1248, 2008 | 610 | 2008 |
| Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications KN Ballantyne, M Goedbloed, R Fang, O Schaap, O Lao, A Wollstein, ... The American Journal of Human Genetics 87 (3), 341-353, 2010 | 475 | 2010 |
| A genetic association between juvenile rheumatoid arthritis and a novel interleukin‐1α polymorphism TL McDowell, JA Symons, R Ploski, ØY FØRre, GW Duff Arthritis & Rheumatism: Official Journal of the American College of …, 1995 | 447 | 1995 |
| Prognostic factors in juvenile rheumatoid arthritis: a case-control study revealing early predictors and outcome after 14.9 years. B FlatØ, G Lien, A Smerdel, O Vinje, K Dale, V Johnston, D SØrskaar, ... The Journal of rheumatology 30 (2), 386-393, 2003 | 353 | 2003 |
| Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypes L Roewer, M Krawczak, S Willuweit, M Nagy, C Alves, A Amorim, ... Forensic science international 118 (2-3), 106-113, 2001 | 343 | 2001 |
| A global analysis of Y-chromosomal haplotype diversity for 23 STR loci J Purps, S Siegert, S Willuweit, M Nagy, C Alves, R Salazar, ... Forensic Science International: Genetics 12, 12-23, 2014 | 290 | 2014 |
| Cytotoxic T-lymphocyte associated antigen 4 gene polymorphisms and autoimmune thyroid disease: a meta-analysis FK Kavvoura, T Akamizu, T Awata, Y Ban, DA Chistiakov, I Frydecka, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 3162-3170, 2007 | 238 | 2007 |
| On the HLA‐DQ(α1*0501, β1*0201)‐associated susceptibility in celiac disease: A possible gene dosage effect of DQB1*0201 R Ploski, J Ek, E Thorsby, LM Sollid Tissue antigens 41 (4), 173-177, 1993 | 229 | 1993 |
| Toward male individualization with rapidly mutating y‐chromosomal short tandem repeats KN Ballantyne, A Ralf, R Aboukhalid, NM Achakzai, MJ Anjos, Q Ayub, ... Human mutation 35 (8), 1021-1032, 2014 | 207 | 2014 |
| Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit M Goedbloed, M Vermeulen, RN Fang, M Lembring, A Wollstein, ... International journal of legal medicine 123, 471-482, 2009 | 176 | 2009 |
| Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis M Kayser, O Lao, K Anslinger, C Augustin, G Bargel, J Edelmann, S Elias, ... Human genetics 117, 428-443, 2005 | 173 | 2005 |
| Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves’ disease in a Polish population: association and gene dose‐dependent correlation with age of … A Skórka, T Bednarczuk, E Bar‐Andziak, J Nauman, R Ploski Clinical Endocrinology 62 (6), 679-682, 2005 | 173 | 2005 |
| Monogenic variants in dystonia: an exome-wide sequencing study M Zech, R Jech, S Boesch, M Škorvánek, S Weber, M Wagner, C Zhao, ... The Lancet Neurology 19 (11), 908-918, 2020 | 154 | 2020 |
| Coexisting polymorphisms of P2Y12 and CYP2C19 genes as a risk factor for persistent platelet activation with clopidogrel LA Malek, B Kisiel, M Spiewak, M Grabowski, KJ Filipiak, G Kostrzewa, ... Circulation Journal 72 (7), 1165-1169, 2008 | 149 | 2008 |
| The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269 GBJ Busby, F Brisighelli, P Sanchez-Diz, E Ramos-Luis, ... Proceedings of the Royal Society B: Biological Sciences 279 (1730), 884-892, 2012 | 147 | 2012 |
| SRGAP1 Is a Candidate Gene for Papillary Thyroid Carcinoma Susceptibility H He, A Bronisz, S Liyanarachchi, R Nagy, W Li, Y Huang, K Akagi, M Saji, ... The Journal of Clinical Endocrinology & Metabolism 98 (5), E973-E980, 2013 | 129 | 2013 |
| CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder SB Wortmann, S Ziętkiewicz, M Kousi, R Szklarczyk, TB Haack, ... The American Journal of Human Genetics 96 (2), 245-257, 2015 | 126 | 2015 |
| M34T and V37I mutations in GJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance A Pollak, A Skórka, M Mueller‐Malesińska, G Kostrzewa, B Kisiel, ... American journal of medical genetics Part A 143 (21), 2534-2543, 2007 | 124 | 2007 |
| Homogeneity and distinctiveness of Polish paternal lineages revealed by Y chromosome microsatellite haplotype analysis R Ploski, M Wozniak, R Pawlowski, D Monies, W Branicki, T Kupiec, ... Human genetics 110, 592-600, 2002 | 120 | 2002 |
