引用次数
引用: 346,540
H-指数: 210
I10-指数 : 508
出版物: 879
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
Pradeep Natarajan , Akhil Pampana , Sarah E Graham , Sanni E Ruotsalainen
Nature Communications 12 ( 1) 2182 -2182
2021
Computationally efficient whole-genome regression for quantitative and binary traits.
Aris Baras , Leland Barnard , Andrey Ziyatdinov , Lukas Habegger
Nature Genetics 1 -7
231
2021
Clonal hematopoiesis associated with epigenetic aging and clinical outcomes.
Daniel Nachun , Ake T Lu , Alexander G Bick , Pradeep Natarajan
Aging Cell
37
2021
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees
Laura Almasy , Thomas D Dyer , Juan M Peralta , Goo Jun
BMC Proceedings 8 ( 1) 1 -9
78
2014
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Pradeep Natarajan , Gina M Peloso , Seyedeh Maryam Zekavat , May Montasser
Nature Communications 9 ( 1) 3391
84
2018
Whole genome sequencing in psychiatric disorders: The WGSPD consortium
Stephan J. Sanders , , Benjamin M. Neale , Hailiang Huang
Nature Neuroscience 20 ( 12) 1661 -1668
92
2017
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Stephan J. Sanders , , Benjamin M. Neale , Hailiang Huang
Nature Neuroscience 21 ( 7) 1017 -1017
3
2018
Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes
Alexander G Bick , Joshua S Weinstock , Satish K Nandakumar , Charles P Fulco
bioRxiv 782748
18
2019
No bias in linkage analysis.
Goncalo Abecasis , Nancy Cox , Mark J. Daly , Leonid Kruglyak
American Journal of Human Genetics 75 ( 4) 722 -723
7
2004
A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia.
Julie Richer , Hannah L. Hill , Yu Wang , Min-Lee Yang
Arteriosclerosis, Thrombosis, and Vascular Biology 40 ( 11) 2686 -2699
22
2020
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
Wenqing Fu , Timothy D O’connor , Goo Jun , Hyun Min Kang
Nature 493 ( 7431) 216 -220
1,028
2013
Genetic Modifiers of Homozygous Beta Zero Thalassemia.
Renzo Galanello , Serena Sanna , Lucia Perseu , Maria Carla Sollaino
Blood 112 ( 11) 1874 -1874
2008
A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.
Yu-Ru Su , Chongzhi Di , Stephanie Bien , Licai Huang
American Journal of Human Genetics 102 ( 5) 904 -919
18
2018
Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease
J. Brent Richards , Fred C. Sweep , Christian Gieger , Tanguy Corre
PLOS Genetics 10 ( 2) 1 -13
157
2014
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus
Anubha Mahajan , Xueling Sim , Hui Jin Ng , Alisa Manning
PLOS Genetics 11 ( 1) e1004876
76
2015
Imputation aware tag SNP selection to improve power for multi-ethnic association studies
Genevieve L. Wojcik , Christian Fuchsberger , Daniel Taliun , Ryan Welch
bioRxiv 105551
3
2017
In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
Scott I. Vrieze , Stephen M. Malone , Uma Vaidyanathan , Alan Kwong
Psychophysiology 51 ( 12) 1309 -1320
27
2014
Whole-genome sequence-based analysis of thyroid function
Peter N Taylor , Eleonora Porcu , Shelby Chew , Purdey J Campbell
Nature Communications 6 ( 1) 5681 -5681
98
2015
Rare and low-frequency coding variants alter human adult height
Eirini Marouli , Mariaelisa Graff , Carolina Medina-Gomez , Ken Sin Lo
Nature 542 ( 7640) 186 -190
563
2017
Genetic association study of age‐related macular degeneration in the Spanish population
María Brión , Manuel Sanchez‐Salorio , Marta Cortón , Maria de la Fuente
Acta Ophthalmologica 89 ( 1)
32
2011