| Gapped BLAST and PSI-BLAST: a new generation of protein database search programs SF Altschul, TL Madden, AA Schäffer, J Zhang, Z Zhang, W Miller, ... Nucleic acids research 25 (17), 3389-3402, 1997 | 71893 | 1997 |
| Faster sequential genetic linkage computations. RW Cottingham Jr, RM Idury, AA Schäffer American journal of human genetics 53 (1), 252, 1993 | 1516 | 1993 |
| Improving the accuracy of PSI-BLAST protein database searches with composition-based statistics and other refinements AA Schäffer, L Aravind, TL Madden, S Shavirin, JL Spouge, YI Wolf, ... Nucleic acids research 29 (14), 2994-3005, 2001 | 1360 | 2001 |
| Inflammatory bowel disease and mutations affecting the interleukin-10 receptor EO Glocker, D Kotlarz, K Boztug, EM Gertz, AA Schäffer, F Noyan, M Perro, ... New England Journal of Medicine 361 (21), 2033-2045, 2009 | 1123 | 2009 |
| STAT3 mutations in the hyper-IgE syndrome SM Holland, FR DeLeo, HZ Elloumi, AP Hsu, G Uzel, N Brodsky, ... New England Journal of Medicine 357 (16), 1608-1619, 2007 | 1013 | 2007 |
| Mapping of a gene for Parkinson's disease to chromosome 4q21-q23 MH Polymeropoulos, JJ Higgins, LI Golbe, WG Johnson, SE Ide, ... Science 274 (5290), 1197-1199, 1996 | 882 | 1996 |
| Protein database searches using compositionally adjusted substitution matrices SF Altschul, JC Wootton, EM Gertz, R Agarwala, A Morgulis, AA Schäffer, ... The FEBS journal 272 (20), 5101-5109, 2005 | 840 | 2005 |
| Avoiding recomputation in linkage analysis AA Schaeffer, SK Gupta, K Shriram, RW Cottingham Jr Human heredity 44 (4), 225-237, 1994 | 738 | 1994 |
| Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency B Grimbacher, A Hutloff, M Schlesier, E Glocker, K Warnatz, R Dräger, ... Nature immunology 4 (3), 261, 2003 | 717 | 2003 |
| Database indexing for production MegaBLAST searches A Morgulis, G Coulouris, Y Raytselis, TL Madden, R Agarwala, ... Bioinformatics 24 (16), 1757-1764, 2008 | 666 | 2008 |
| A homozygous CARD9 mutation in a family with susceptibility to fungal infections EO Glocker, A Hennigs, M Nabavi, AA Schäffer, C Woellner, U Salzer, ... New England Journal of Medicine 361 (18), 1727-1735, 2009 | 632 | 2009 |
| Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans U Salzer, HM Chapel, ADB Webster, Q Pan-Hammarström, ... Nature genetics 37 (8), 820, 2005 | 620 | 2005 |
| Graph spanners D Peleg, AA Schäffer Journal of graph theory 13 (1), 99-116, 1989 | 592 | 1989 |
| Domain enhanced lookup time accelerated BLAST GM Boratyn, AA Schäffer, R Agarwala, SF Altschul, DJ Lipman, ... Biology direct 7 (1), 12, 2012 | 466 | 2012 |
| A genetic linkage map of microsatellites in the domestic cat (Felis catus) M Menotti-Raymond, VA David, LA Lyons, AA Schäffer, JF Tomlin, ... Genomics 57 (1), 9-23, 1999 | 458 | 1999 |
| Genetic heterogeneity and clonal evolution underlying development of asynchronous metastasis in human breast cancer T Kuukasjärvi, R Karhu, M Tanner, M Kähkönen, A Schäffer, N Nupponen, ... Cancer research 57 (8), 1597-1604, 1997 | 448 | 1997 |
| Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25. 2-27. H Matsumine, M Saito, S Shimoda-Matsubayashi, H Tanaka, A Ishikawa, ... American journal of human genetics 60 (3), 588, 1997 | 443 | 1997 |
| HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease) C Klein, M Grudzien, G Appaswamy, M Germeshausen, I Sandrock, ... Nature genetics 39 (1), 86, 2007 | 442 | 2007 |
| Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations D Schubert, C Bode, R Kenefeck, TZ Hou, JB Wing, A Kennedy, ... Nature medicine 20 (12), 1410, 2014 | 430 | 2014 |
| Genetic linkage of hyper-IgE syndrome to chromosome 4 B Grimbacher, AA Schäffer, SM Holland, J Davis, JI Gallin, HL Malech, ... The American Journal of Human Genetics 65 (3), 735-744, 1999 | 366 | 1999 |
Stephen AltschulNCBI NLM NIHVerified email at nih.gov
