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Alejandro Schaffer
Alejandro Schaffer
Computer Scientist, National Institutes of Health
E-mailová adresa ověřena na: nih.gov - Domovská stránka
Název
Citace
Citace
Rok
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
838351997
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
15882001
Faster sequential genetic linkage computations.
RW Cottingham Jr, RM Idury, AA Schäffer
American journal of human genetics 53 (1), 252, 1993
15871993
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
15582009
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
13232007
Database indexing for production MegaBLAST searches
A Morgulis, G Coulouris, Y Raytselis, TL Madden, R Agarwala, ...
Bioinformatics 24 (16), 1757-1764, 2008
12572008
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
12252005
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
10861996
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), 261-268, 2003
8582003
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
8252009
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), 1410-1416, 2014
8072014
Domain enhanced lookup time accelerated BLAST
GM Boratyn, AA Schäffer, R Agarwala, SF Altschul, DJ Lipman, ...
Biology direct 7, 1-14, 2012
8012012
Avoiding recomputation in linkage analysis
AA Schaeffer, SK Gupta, K Shriram, RW Cottingham, Jr
Human heredity 44 (4), 225-237, 1994
7861994
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), 820-828, 2005
7392005
Graph spanners
D Peleg, AA Schäffer
Journal of graph theory 13 (1), 99-116, 1989
7021989
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
5551999
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
C Klein, M Grudzien, G Appaswamy, M Germeshausen, I Sandrock, ...
Nature genetics 39 (1), 86-92, 2007
5482007
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
5441997
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
G Lopez-Herrera, G Tampella, Q Pan-Hammarström, P Herholz, ...
The American Journal of Human Genetics 90 (6), 986-1001, 2012
5132012
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
4991997
Systém momentálně nemůže danou operaci provést. Zkuste to znovu později.
Články 1–20