| Year |
Citation |
Score |
| 2018 |
Ullah E, Mall R, Abbas MM, Kunji K, Nato AQ, Bensmail H, Wijsman EM, Saad M. Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees. Genome Research. PMID 30514702 DOI: 10.1101/Gr.236315.118 |
0.381 |
|
| 2018 |
Nafikov RA, Nato AQ, Sohi H, Wang B, Brown L, Horimoto AR, Vardarajan BN, Barral SM, Tosto G, Mayeux RP, Thornton TA, Blue E, Wijsman EM. Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. Genetic Epidemiology. PMID 29862559 DOI: 10.1002/Gepi.22133 |
0.411 |
|
| 2018 |
Naj AC, Lin H, Vardarajan BN, White S, Lancour D, Ma Y, Schmidt M, Sun F, Butkiewicz M, Bush WS, Kunkle BW, Malamon J, Amin N, Choi SH, Hamilton-Nelson KL, ... ... Nato AQ, et al. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project. Genomics. PMID 29857119 DOI: 10.1016/J.Ygeno.2018.05.004 |
0.374 |
|
| 2018 |
Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C, DeStefano A, Farrer LA, Goate A, Haines J, Jaworski J, ... ... Nato AQ, et al. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dementia and Geriatric Cognitive Disorders. 45: 1-17. PMID 29486463 DOI: 10.1159/000485503 |
0.316 |
|
| 2017 |
Kunji K, Ullah E, Nato AQ, Wijsman EM, Saad M. GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data. Bioinformatics (Oxford, England). PMID 29267877 DOI: 10.1093/Bioinformatics/Btx782 |
0.41 |
|
| 2016 |
Blue EM, Brown LA, Conomos MP, Kirk JL, Nato AQ, Popejoy AB, Raffa J, Ranola J, Wijsman EM, Thornton T. Estimating relationships between phenotypes and subjects drawn from admixed families. Bmc Proceedings. 10: 357-362. PMID 27980662 DOI: 10.1186/S12919-016-0056-3 |
0.333 |
|
| 2016 |
Saad M, Nato AQ, Grimson FL, Lewis SM, Brown LA, Blue EM, Thornton TA, Thompson EA, Wijsman EM. Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data. Bmc Proceedings. 10: 295-301. PMID 27980652 DOI: 10.1186/S12919-016-0046-5 |
0.36 |
|
| 2016 |
Peter B, Wijsman EM, Nato AQ, Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. Plos One. 11: e0153864. PMID 27120335 DOI: 10.1371/Journal.Pone.0153864 |
0.373 |
|
| 2016 |
Ahmad S, Amin N, Blue E, Lee SJvd, Nato AQ, Sohi H, Wang B, Boerwinkle E, DeStefano AL, Wijsman E, Duijn CMv. Genomewide Linkage Analysis Identifies Novel Candidate Genes For Alzheimer’S Disease Alzheimers & Dementia. 12: 196. DOI: 10.1016/J.Jalz.2016.06.341 |
0.36 |
|
| 2015 |
Nato AQ, Chapman NH, Sohi HK, Nguyen HD, Brkanac Z, Wijsman EM. PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers. Bioinformatics (Oxford, England). PMID 26231429 DOI: 10.1093/Bioinformatics/Btv444 |
0.382 |
|
| 2015 |
Chapman NH, Nato AQ, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics. 134: 1055-68. PMID 26204995 DOI: 10.1007/S00439-015-1585-Y |
0.399 |
|
| 2015 |
Li BI, Matteson PG, Ababon MF, Nato AQ, Lin Y, Nanda V, Matise TC, Millonig JH. The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation. Developmental Biology. 402: 17-31. PMID 25753732 DOI: 10.1016/J.Ydbio.2015.02.007 |
0.509 |
|
| 2014 |
Musolf A, Nato AQ, Londono D, Zhou L, Matise TC, Gordon D. Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. Bmc Proceedings. 8: S81. PMID 25519410 DOI: 10.1186/1753-6561-8-S1-S81 |
0.573 |
|
| 2013 |
Dumitrescu L, Carty CL, Franceschini N, Hindorff LA, Cole SA, Bůžková P, Schumacher FR, Eaton CB, Goodloe RJ, Duggan DJ, Haessler J, Cochran B, Henderson BE, Cheng I, Johnson KC, ... ... Nato AQ, et al. No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population. Human Genetics. 132: 1427-31. PMID 24100633 DOI: 10.1007/S00439-013-1375-3 |
0.34 |
|
| 2013 |
Dumitrescu L, Carty CL, Franceschini N, Hindorff LA, Cole SA, Bůžková P, Schumacher FR, Eaton CB, Goodloe RJ, Duggan DJ, Haessler J, Cochran B, Henderson BE, Cheng I, Johnson KC, ... ... Nato AQ, et al. Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study. Annals of Human Genetics. 77: 416-25. PMID 23808484 DOI: 10.1111/Ahg.12027 |
0.359 |
|
| 2013 |
Zhang L, Buzkova P, Wassel CL, Roman MJ, North KE, Crawford DC, Boston J, Brown-Gentry KD, Cole SA, Deelman E, Goodloe R, Wilson S, Heiss G, Jenny NS, Jorgensen NW, ... ... Nato AQ, et al. Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study. Atherosclerosis. 228: 390-9. PMID 23587283 DOI: 10.1016/J.Atherosclerosis.2013.02.038 |
0.558 |
|
| 2012 |
Kim W, Londono D, Zhou L, Xing J, Nato AQ, Musolf A, Matise TC, Finch SJ, Gordon D. Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. Human Heredity. 74: 172-83. PMID 23594495 DOI: 10.1159/000346824 |
0.558 |
|
| 2012 |
Perdry H, Müller-Myhsok B, Clerget-Darpoux F, Génin E, Sahbatou M, Kim W, Londono D, Kazma R, Cardin NJ, Witte JS, Asimit JL, Zeggini E, Jouan L, Gauthier J, Dion PA, ... ... Nato AQ, et al. Contents Vol. 74, 2012 Human Heredity. 74. DOI: 10.1159/000346894 |
0.466 |
|
| 2007 |
Shimada MK, Panchapakesan K, Tishkoff SA, Nato AQ, Hey J. Divergent haplotypes and human history as revealed in a worldwide survey of X-linked DNA sequence variation. Molecular Biology and Evolution. 24: 687-98. PMID 17175528 DOI: 10.1093/Molbev/Msl196 |
0.315 |
|
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