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h5 指数:92
h5 中位数:124

h5 指数是指在过去整整 5 年中所发表文章的 h 指数。h 指在 2018-2022 年间发表的 h 篇文章每篇至少都被引用过 h 次的最大值。隐藏

出版物的 h5 中位数，是指出版物的 h5 指数所涵盖的所有文章获得的引用次数的中位值。隐藏

#6 Genetics & Genomics

标题/作者	引用次数	年份
A One-Penny Imputed Genome from Next-Generation Reference Panels BL Browning, Y Zhou, SR Browning The American Journal of Human Genetics 103 (3), 338-348	976	2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ... The American Journal of Human Genetics 104 (1), 21-34	749	2019
Leveraging Polygenic Functional Enrichment to Improve GWAS Power G Kichaev, G Bhatia, PR Loh, S Gazal, K Burch, MK Freund, A Schoech, ... The American Journal of Human Genetics 104 (1), 65-75	690	2019
The Post-GWAS Era: From Association to Function MD Gallagher, AS Chen-Plotkin The American Journal of Human Genetics 102 (5), 717-730	632	2018
The Expanding Landscape of Alternative Splicing Variation in Human Populations E Park, Z Pan, Z Zhang, L Lin, Y Xing The American Journal of Human Genetics 102 (1), 11-26	294	2018
Genome Analyses of> 200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders S Ligthart, A Vaez, U Võsa, MG Stathopoulou, PS de Vries, BP Prins, ... The American Journal of Human Genetics 103 (5), 691-706	285	2018
Integrating Genomics into Healthcare: A Global Responsibility Z Stark, L Dolman, TA Manolio, B Ozenberger, SL Hill, MJ Caulfied, ... The American Journal of Human Genetics 104 (1), 13-20	266	2019
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease HD Gonorazky, S Naumenko, AK Ramani, V Nelakuditi, P Mashouri, ... The American Journal of Human Genetics 104 (3), 466-483	223	2019
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects C Medina-Gomez, JP Kemp, K Trajanoska, J Luan, A Chesi, TS Ahluwalia, ... The American Journal of Human Genetics 102 (1), 88-102	220	2018
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands KRM van der Meij, EA Sistermans, MVE Macville, SJC Stevens, CJ Bax, ... The American Journal of Human Genetics 105 (6), 1091-1101	219	2019
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants SF Kingsmore, JA Cakici, MM Clark, M Gaughran, M Feddock, S Batalov, ... The American Journal of Human Genetics 105 (4), 719-733	215	2019
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease E Cornec-Le Gall, RJ Olson, W Besse, CM Heyer, VG Gainullin, JM Smith, ... The American Journal of Human Genetics 102 (5), 832-844	212	2018
Comparing Within-and Between-Family Polygenic Score Prediction S Selzam, SJ Ritchie, JB Pingault, CA Reynolds, PF O’Reilly, R Plomin The American Journal of Human Genetics 105 (2), 351-363	204	2019
The Genetic Landscape of Diamond-Blackfan Anemia JC Ulirsch, JM Verboon, S Kazerounian, MH Guo, D Yuan, LS Ludwig, ... The American Journal of Human Genetics 103 (6), 930-947	204	2018
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders Y Tian, JL Wang, W Huang, S Zeng, B Jiao, Z Liu, Z Chen, Y Li, Y Wang, ... The American Journal of Human Genetics 105 (1), 166-176	194	2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ... The American Journal of Human Genetics 104 (6), 1182-1201	191	2019
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282	185	2019
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes H Azaiez, KT Booth, SS Ephraim, B Crone, EA Black-Ziegelbein, ... The American Journal of Human Genetics 103 (4), 484-497	185	2018
ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies Y Liu, S Chen, Z Li, AC Morrison, E Boerwinkle, X Lin The American Journal of Human Genetics 104 (3), 410-421	179	2019
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders V Faundes, WG Newman, L Bernardini, N Canham, J Clayton-Smith, ... The American Journal of Human Genetics 102 (1), 175-187	177	2018

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