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h5 指数:70
h5 中位数:110

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

#11 Genetics & Genomics

标题/作者	引用次数	年份
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. S Richards, N Aziz, S Bale, D Bick, S Das, J Gastier-Foster, WW Grody, ... Genetics in medicine: official journal of the American College of Medical …	7275	2015
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2. 0): a policy statement of the American College of Medical Genetics and Genomics SS Kalia, K Adelman, SJ Bale, WK Chung, C Eng, JP Evans, GE Herman, ... Genetics in Medicine 19 (2), 249	712	2017
The genetic landscape of Alzheimer disease: clinical implications and perspectives. CC Van, CB Van, K Sleegers Genetics in medicine: official journal of the American College of Medical …	438	2016
Clinical application of whole-exome sequencing across clinical indications K Retterer, J Juusola, MT Cho, P Vitazka, F Millan, F Gibellini, ... Genetics in Medicine 18 (7), 696	369	2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. R Walsh, KL Thomson, JS Ware, BH Funke, J Woodley, KJ McGuire, ... Genetics in medicine: official journal of the American College of Medical …	324	2017
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics AR Gregg, BG Skotko, JL Benkendorf, KG Monaghan, K Bajaj, RG Best, ... Genetics in Medicine 18 (10), 1056	321	2016
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions KD Farwell, L Shahmirzadi, D El-khechen, Z Powis, EC Chao, BT Davis, ... Genetics in Medicine 17 (7), 578	315	2015
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment H Hampel, RL Bennett, A Buchanan, R Pearlman, GL Wiesner Genetics in Medicine 17 (1), 70	241	2015
Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing Y Xue, A Ankala, WR Wilcox, MR Hegde Genetics in Medicine 17 (6), 444	218	2015
Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society S Parikh, A Goldstein, MK Koenig, F Scaglia, GM Enns, R Saneto, ... Genetics in Medicine 17 (9), 689	217	2015
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios X Zhu, S Petrovski, P Xie, EK Ruzzo, Y Lu, KM Mcsweeney, B Ben-zeev, ... Genetics in Medicine 17 (10), 774	213	2015
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity AA Alfares, MA Kelly, G Mcdermott, BH Funke, MS Lebo, SB Baxter, ... Genetics in Medicine 17 (11), 880	210	2015
Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC). KE Caudle, HM Dunnenberger, RR Freimuth, JF Peterson, JD Burlison, ... Genetics in medicine: official journal of the American College of Medical …	205	2017
Prediction of CYP2D6 phenotype from genotype across world populations. A Gaedigk, K Sangkuhl, M Whirl-Carrillo, T Klein, JS Leeder Genetics in Medicine: Official Journal of the American College of Medical …	205	2016
A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders Z Stark, TY Tan, B Chong, GR Brett, P Yap, M Walsh, A Yeung, H Peters, ... Genetics in Medicine 18 (11), 1090	191	2016
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. ACMG Board of Directors Genetics in medicine: official journal of the American College of Medical …	186	2015
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy KL Helbig, KDF Hagman, DN Shinde, C Mroske, Z Powis, S Li, S Tang, ... Genetics in Medicine 18 (9), 898	175	2016
Using high-resolution variant frequencies to empower clinical genome interpretation. N Whiffin, E Minikel, R Walsh, AH O'Donnell-Luria, K Karczewski, AY Ing, ... Genetics in medicine: official journal of the American College of Medical …	162	2017
Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria. K Nykamp, M Anderson, M Powers, J Garcia, B Herrera, YY Ho, ... Genetics in medicine: official journal of the American College of Medical …	156	2017
The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research. DJ Carey, SN Fetterolf, FD Davis, WA Faucett, HL Kirchner, U Mirshahi, ... Genetics in medicine: official journal of the American College of Medical …	151	2016

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