| Evolutionary and biomedical insights from the rhesus macaque genome RA Gibbs, J Rogers, MG Katze, R Bumgarner, GM Weinstock, ER Mardis, ... science 316 (5822), 222-234, 2007 | 1468 | 2007 |
| X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein J Kere, AK Srivastava, O Montonen, J Zonana, N Thomas, B Ferguson, ... Nature genetics 13 (4), 409-416, 1996 | 934 | 1996 |
| SR proteins and splicing control 1569 JL Manley, R Tacke, BLM Hogan, KL Friedman, JD Diller, BM Ferguson, ... Genes Dev 10, 1569-1579, 1996 | 867 | 1996 |
| A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO) J Zonana, ME Elder, LC Schneider, SJ Orlow, C Moss, M Golabi, ... The American Journal of Human Genetics 67 (6), 1555-1562, 2000 | 578 | 2000 |
| Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia AW Monreal, BM Ferguson, DJ Headon, SL Street, PA Overbeek, ... Nature genetics 22 (4), 366-369, 1999 | 471 | 1999 |
| Gene defect in ectodermal dysplasia implicates a death domain adapter in development DJ Headon, SA Emmal, BM Ferguson, AS Tucker, MJ Justice, PT Sharpe, ... Nature 414 (6866), 913-916, 2001 | 446 | 2001 |
| A position effect on the time of replication origin activation in yeast BM Ferguson, WL Fangman Cell 68 (2), 333-339, 1992 | 354 | 1992 |
| Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations AW Monreal, J Zonana, B Ferguson The American Journal of Human Genetics 63 (2), 380-389, 1998 | 277 | 1998 |
| A yeast origin of replication is activated late in S phase BM Ferguson, BJ Brewer, AE Reynolds, WL Fangman Cell 65 (3), 507-515, 1991 | 257 | 1991 |
| Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations JS Orange, SR Brodeur, A Jain, FA Bonilla, LC Schneider, R Kretschmer, ... The Journal of clinical investigation 109 (11), 1501-1509, 2002 | 250 | 2002 |
| Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A P Schneider, SL Street, O Gaide, S Hertig, A Tardivel, J Tschopp, ... Journal of Biological Chemistry 276 (22), 18819-18827, 2001 | 249 | 2001 |
| Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis AS Tucker, DJ Headon, P Schneider, BM Ferguson, P Overbeek, ... Development 127 (21), 4691-4700, 2000 | 245 | 2000 |
| Cloning of Tabby, the Murine Homolog of the Human EDA Gene: Evidence for a Membrane-Associated Protein with a Short Collagenous Domain BM Ferguson, N Brockdorff, E Formstone, T Ngyuen, JE Kronmiller, ... Human Molecular Genetics 6 (9), 1589-1594, 1997 | 208 | 1997 |
| Multiple determinants controlling activation of yeast replication origins late in S phase. KL Friedman, JD Diller, BM Ferguson, SV Nyland, BJ Brewer, ... Genes & development 10 (13), 1595-1607, 1996 | 197 | 1996 |
| Demographic histories and patterns of linkage disequilibrium in Chinese and Indian rhesus macaques RD Hernandez, MJ Hubisz, DA Wheeler, DG Smith, B Ferguson, J Rogers, ... Science 316 (5822), 240-243, 2007 | 192 | 2007 |
| A new rhesus macaque assembly and annotation for next-generation sequencing analyses AV Zimin, AS Cornish, MD Maudhoo, RM Gibbs, X Zhang, S Pandey, ... Biology direct 9, 1-15, 2014 | 185 | 2014 |
| Mutation of RGA1, which encodes a putative GTPase-activating protein for the polarity-establishment protein Cdc42p, activates the pheromone-response pathway in the yeast … BJ Stevenson, B Ferguson, C De Virgilio, E Bi, JR Pringle, G Ammerer, ... Genes & development 9 (23), 2949-2963, 1995 | 177 | 1995 |
| Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia Y Chen, SS Molloy, L Thomas, J Gambee, HP Bächinger, B Ferguson, ... Proceedings of the National Academy of Sciences 98 (13), 7218-7223, 2001 | 156 | 2001 |
| Rhesus monkeys and humans share common susceptibility genes for age-related macular disease PJ Francis, B Appukuttan, E Simmons, N Landauer, J Stoddard, S Hamon, ... Human molecular genetics 17 (17), 2673-2680, 2008 | 115 | 2008 |
| Single nucleotide polymorphisms (SNPs) distinguish Indian-origin and Chinese-origin rhesus macaques (Macaca mulatta) B Ferguson, SL Street, H Wright, C Pearson, Y Jia, SL Thompson, ... BMC genomics 8, 1-9, 2007 | 111 | 2007 |
