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Stephen F. Kingsmore
Stephen F. Kingsmore
Rady Children's Institute for Genomic Medicine
Verified email at rchsd.org - Homepage
Title
Cited by
Cited by
Year
Alternative isoform regulation in human tissue transcriptomes
ET Wang, R Sandberg, S Luo, I Khrebtukova, L Zhang, C Mayr, ...
Nature 456 (7221), 470-476, 2008
51042008
Comprehensive human genome amplification using multiple displacement amplification
FB Dean, S Hosono, L Fang, X Wu, AF Faruqi, P Bray-Ward, Z Sun, ...
Proceedings of the National Academy of Sciences 99 (8), 5261-5266, 2002
17132002
Multiplexed protein measurement: technologies and applications of protein and antibody arrays
SF Kingsmore
Nature reviews Drug discovery 5 (4), 310-321, 2006
8312006
Immunoassays with rolling circle DNA amplification: a versatile platform for ultrasensitive antigen detection
B Schweitzer, S Wiltshire, J Lambert, S O'Malley, K Kukanskis, Z Zhu, ...
Proceedings of the National Academy of Sciences 97 (18), 10113-10119, 2000
7622000
Carrier testing for severe childhood recessive diseases by next-generation sequencing
CJ Bell, DL Dinwiddie, NA Miller, SL Hateley, EE Ganusova, J Mudge, ...
Science translational medicine 3 (65), 65ra4-65ra4, 2011
7612011
Multiplexed protein profiling on microarrays by rolling-circle amplification
B Schweitzer, S Roberts, B Grimwade, W Shao, M Wang, Q Fu, Q Shu, ...
Nature biotechnology 20 (4), 359-365, 2002
7262002
Unbiased whole-genome amplification directly from clinical samples
S Hosono, AF Faruqi, FB Dean, Y Du, Z Sun, X Wu, J Du, SF Kingsmore, ...
Genome research 13 (5), 954-964, 2003
6112003
Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units
CJ Saunders, NA Miller, SE Soden, DL Dinwiddie, A Noll, NA Alnadi, ...
Science translational medicine 4 (154), 154ra135-154ra135, 2012
5902012
Identification of the homologous beige and Chediak–Higashi syndrome genes
MDFS Barbosa, QA Nguyen, VT Tchernev, JA Ashley, JC Detter, ...
Nature 382 (6588), 262-265, 1996
5791996
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
SE Baranzini, J Mudge, JC Van Velkinburgh, P Khankhanian, ...
Nature 464 (7293), 1351-1356, 2010
5192010
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
W Li, Q Zhang, N Oiso, EK Novak, R Gautam, EP O'Brien, CL Tinsley, ...
Nature genetics 35 (1), 84-89, 2003
4672003
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders
SE Soden, CJ Saunders, LK Willig, EG Farrow, LD Smith, JE Petrikin, ...
Science translational medicine 6 (265), 265ra168-265ra168, 2014
4572014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations
JD Milner, TP Vogel, L Forbes, CA Ma, A Stray-Pedersen, JE Niemela, ...
Blood, The Journal of the American Society of Hematology 125 (4), 591-599, 2015
4542015
Gene expression signatures diagnose influenza and other symptomatic respiratory viral infections in humans
AK Zaas, M Chen, J Varkey, T Veldman, AO Hero III, J Lucas, Y Huang, ...
Cell host & microbe 6 (3), 207-217, 2009
3882009
A highly annotated whole-genome sequence of a Korean individual
JI Kim, YS Ju, H Park, S Kim, S Lee, JH Yi, J Mudge, NA Miller, D Hong, ...
nature 460 (7258), 1011-1015, 2009
3822009
An integrated clinico-metabolomic model improves prediction of death in sepsis
RJ Langley, EL Tsalik, JC Velkinburgh, SW Glickman, BJ Rice, C Wang, ...
Science translational medicine 5 (195), 195ra95-195ra95, 2013
3802013
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases
MM Clark, Z Stark, L Farnaes, TY Tan, SM White, D Dimmock, ...
NPJ genomic medicine 3 (1), 1-10, 2018
3312018
Combining nucleic acid amplification and detection
B Schweitzer, S Kingsmore
Current opinion in biotechnology 12 (1), 21-27, 2001
3212001
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings
Lancet Respiratory Medicine, 2015
2912015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases.
KSF Miller NA, Farrow EG, Gibson M, Willig LK, Twist G, Yoo B, Marrs T ...
Genomic Medicine 7, 100, 2015
265*2015
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