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Title
Cited by
Cited by
Year
A haplotype map of the human genome
KW TSUI, MMY WAYE
Nature 437 (7063), 1299-1320, 2005
10364*2005
The international HapMap project
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...
Nature Publishing Group, 2003
61762003
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
27072014
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
21812007
A note on exact tests of Hardy-Weinberg equilibrium
JE Wigginton, DJ Cutler, GR Abecasis
The American Journal of Human Genetics 76 (5), 887-893, 2005
16742005
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
16582020
Comparative analyses of multi-species sequences from targeted genomic regions
JW Thomas, JW Touchman, RW Blakesley, GG Bouffard, ...
Nature 424 (6950), 788-793, 2003
7872003
Genomic alterations in cultured human embryonic stem cells
A Maitra, DE Arking, N Shivapurkar, M Ikeda, V Stastny, K Kassauei, G Sui, ...
Nature genetics 37 (10), 1099-1103, 2005
7692005
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
DE Arking, DJ Cutler, CW Brune, TM Teslovich, K West, M Ikeda, A Rea, ...
The American Journal of Human Genetics 82 (1), 160-164, 2008
7662008
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk
ES Emison, AS McCallion, CS Kashuk, RT Bush, E Grice, S Lin, ...
Nature 434 (7035), 857-863, 2005
5162005
Microarray-based genomic selection for high-throughput resequencing
DT Okou, KM Steinberg, C Middle, DJ Cutler, TJ Albert, ME Zwick
Nature methods 4 (11), 907-909, 2007
4822007
High-throughput variation detection and genotyping using microarrays
DJ Cutler, ME Zwick, MM Carrasquillo, CT Yohn, KP Tobin, C Kashuk, ...
Genome research 11 (11), 1913-1925, 2001
4282001
A comparison of phasing algorithms for trios and unrelated individuals
J Marchini, D Cutler, N Patterson, M Stephens, E Eskin, E Halperin, S Lin, ...
The American Journal of Human Genetics 78 (3), 437-450, 2006
3822006
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
JA Kosmicki, KE Samocha, DP Howrigan, SJ Sanders, K Slowikowski, ...
Nature genetics 49 (4), 504-510, 2017
3252017
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13. 2
FA Wright, LJ Strug, VK Doshi, CW Commander, SM Blackman, L Sun, ...
Nature genetics 43 (6), 539-546, 2011
2842011
Microdeletions of 3q29 confer high risk for schizophrenia
JG Mulle, AF Dodd, JA McGrath, PS Wolyniec, AA Mitchell, AC Shetty, ...
The American Journal of Human Genetics 87 (2), 229-236, 2010
2522010
Autosomal recessive causes likely in early-onset Alzheimer disease
TS Wingo, JJ Lah, AI Levey, DJ Cutler
Archives of neurology 69 (1), 59-64, 2012
2472012
Haplotype inference in random population samples
S Lin, DJ Cutler, ME Zwick, A Chakravarti
The American Journal of Human Genetics 71 (5), 1129-1137, 2002
2442002
Heritability of lung disease severity in cystic fibrosis
LL Vanscoy, SM Blackman, JM Collaco, A Bowers, T Lai, K Naughton, ...
American journal of respiratory and critical care medicine 175 (10), 1036-1043, 2007
2392007
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet–Biedl patients with two mutations at a second BBS locus
JL Badano, JC Kim, BE Hoskins, RA Lewis, SJ Ansley, DJ Cutler, ...
Human molecular genetics 12 (14), 1651-1659, 2003
2392003
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