| ZMM proteins during meiosis: crossover artists at work A Lynn, R Soucek, GV Börner Chromosome Research 15, 591-605, 2007 | 340 | 2007 |
| Covariation of synaptonemal complex length and mammalian meiotic exchange rates A Lynn, KE Koehler, LA Judis, ER Chan, JP Cherry, S Schwartz, A Seftel, ... Science 296 (5576), 2222-2225, 2002 | 313 | 2002 |
| Mutations in CDMP1 cause autosomal dominant brachydactyly type C A Polinkovsky, NH Robin, JT Thomas, M Irons, A Lynn, FR Goodman, ... Nature genetics 17 (1), 18-19, 1997 | 296 | 1997 |
| Variation in human meiotic recombination A Lynn, T Ashley, T Hassold Annu. Rev. Genomics Hum. Genet. 5, 317-349, 2004 | 201 | 2004 |
| Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22. 3. H Chen, C Rossier, MD Lalioti, A Lynn, A Chakravarti, G Perrin, ... American journal of human genetics 59 (1), 66, 1996 | 151 | 1996 |
| Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains KE Koehler, JP Cherry, A Lynn, PA Hunt, TJ Hassold Genetics 162 (1), 297-306, 2002 | 140 | 2002 |
| Family history and perceptions about risk and prevention for chronic diseases in primary care: a report from the Family Healthware™ Impact Trial LS Acheson, C Wang, SJ Zyzanski, A Lynn, MT Ruffin, R Gramling, ... Genetics in Medicine 12 (4), 212-218, 2010 | 105 | 2010 |
| Genetic epidemiology of rheumatoid arthritis. AH Lynn, CK Kwoh, CM Venglish, CE Aston, A Chakravarti American journal of human genetics 57 (1), 150, 1995 | 99 | 1995 |
| A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans BA Thiel, A Chakravarti, RS Cooper, A Luke, S Lewis, A Lynn, H Tiwari, ... American journal of hypertension 16 (2), 151-153, 2003 | 80 | 2003 |
| Sex, not genotype, determines recombination levels in mice A Lynn, S Schrump, J Cherry, T Hassold, P Hunt The American Journal of Human Genetics 77 (4), 670-675, 2005 | 74 | 2005 |
| Cytological studies of meiotic recombination in human males T Hassold, L Judis, ER Chan, S Schwartz, A Seftel, A Lynn Cytogenetic and genome research 107 (3-4), 249-255, 2004 | 69 | 2004 |
| Patterns of meiotic recombination on the long arm of human chromosome 21 A Lynn, C Kashuk, MB Petersen, JA Bailey, DR Cox, SE Antonarakis, ... Genome research 10 (9), 1319-1332, 2000 | 66 | 2000 |
| Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22. 3 H Chen, C Rossier, Y Nakamura, A Lynn, A Chakravarti, SE Antonarakis Genomics 41 (2), 193-200, 1997 | 52 | 1997 |
| Age, sex, and the familial risk of rheumatoid arthritis CK Kwoh, C Venglish, AH Lynn, DM Whitley, E Young, A Chakravarti American journal of epidemiology 144 (1), 15-24, 1996 | 43 | 1996 |
| A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. JL Blouin, DH Christie, A Gos, A Lynn, MA Morris, DH Ledbetter, ... American journal of human genetics 57 (2), 388, 1995 | 41 | 1995 |
| Autosomal dominant acute necrotizing encephalopathy maps to 2q12. 1‐2q13 DE Neilson, HS Feiler, KC Wilhelmsen, A Lynn, RM Eiben, DS Kerr, ... Annals of Neurology: Official Journal of the American Neurological …, 2004 | 39 | 2004 |
| Sleep-related epilepsy in the A/J mouse KP Strohl, L Gallaugher, A Lynn, L Friedman, A Hill, JB Singer, ES Lander, ... Sleep 30 (2), 169-176, 2007 | 31 | 2007 |
| Two sequence-ready contigs spanning the two copies of a 200-kb duplication on human 21q: partial sequence and polymorphisms MC Potier, A Dutriaux, R Orti, J Groet, N Gibelin, G Karadima, G Lutfalla, ... Genomics 51 (3), 417-426, 1998 | 26 | 1998 |
| Segregation analysis of microcephaly T Cohen, M Zeitune, BC McGillivray, JG Hall, AH Lynn, CE Aston, ... American journal of medical genetics 65 (3), 226-234, 1996 | 11 | 1996 |
| The genetic architecture of Alzheimer disease risk in the Ohio and Indiana Amish MD Osterman, YE Song, LD Adams, RA Laux, LJ Caywood, MB Prough, ... Human Genetics and Genomics Advances 3 (3), 2022 | 2 | 2022 |
