中国学者近期发表的论文
1.	Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. Author: Kwong A, Shin VY, Ho JC, Kang E, Nakamura S, Teo SH, Lee AS, Sng JH, Ginsburg OM, Kurian AW, Weitzel JN, Siu MT, Law FB, Chan TL, Narod SA, Ford JM, Ma ES, Kim SW. Journal: J Med Genet. 2016 Jan;53(1):15-23. doi: 10.1136/jmedgenet-2015-103132. Epub 2015 Jul 17. Review.    PubMed
2.	CRISPR-Cas9 for medical genetic screens: applications and future perspectives. Author: Xue HY, Ji LJ, Gao AM, Liu P, He JD, Lu XJ. Journal: J Med Genet. 2016 Feb;53(2):91-7. doi: 10.1136/jmedgenet-2015-103409. Epub 2015 Dec 16. Review.    PubMed
3.	Current needs for human and medical genomics research infrastructure in low and middle income countries. Author: Forero DA, Wonkam A, Wang W, Laissue P, López-Correa C, Fernández-López JC, Mugasimangalam R, Perry G. Journal: J Med Genet. 2016 Jul;53(7):438-40. doi: 10.1136/jmedgenet-2015-103631. Epub 2016 Jan 6. No abstract available.     PubMed
4.	No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Author: Easton DF, Lesueur F, Decker B, Michailidou K, Li J, Allen J, Luccarini C, Pooley KA, Shah M, Bolla MK, Wang Q, Dennis J, Ahmad J, Thompson ER, Damiola F, Pertesi M, Voegele C, Mebirouk N, Robinot N, Durand G, Forey N, Luben RN, Ahmed S, Aittomäki K, Anton-Culver H, Arndt V; Australian Ovarian Cancer Study Group, Baynes C, Beckman MW, Benitez J, Van Den Berg D, Blot WJ, Bogdanova NV, Bojesen SE, Brenner H, Chang-Claude J, Chia KS, Choi JY, Conroy DM, Cox A, Cross SS, Czene K, Darabi H, Devilee P, Eriksson M, Fasching PA, Figueroa J, Flyger H, Fostira F, García-Closas M, Giles GG, Glendon G, González-Neira A, Guénel P, Haiman CA, Hall P, Hart SN, Hartman M, Hooning MJ, Hsiung CN, Ito H, Jakubowska A, James PA, John EM, Johnson N, Jones M, Kabisch M, Kang D; kConFab Investigators, Kosma VM, Kristensen V, Lambrechts D, Li N; Lifepool Investigators, Lindblom A, Long J, Lophatananon A, Lubinski J, Mannermaa A, Manoukian S, Margolin S, Matsuo K, Meindl A, Mitchell G, Muir K; NBCS Investigators, Nevelsteen I, van den Ouweland A, Peterlongo P, Phuah SY, Pylkäs K, Rowley SM, Sangrajrang S, Schmutzler RK, Shen CY, Shu XO, Southey MC, Surowy H, Swerdlow A, Teo SH, Tollenaar RA, Tomlinson I, Torres D, Truong T, Vachon C, Verhoef S, Wong-Brown M, Zheng W, Zheng Y, Nevanlinna H, Scott RJ, Andrulis IL, Wu AH, Hopper JL, Couch FJ, Winqvist R, Burwinkel B, Sawyer EJ, Schmidt MK, Rudolph A, Dörk T, Brauch H, Hamann U, Neuhausen SL, Milne RL, Fletcher O, Pharoah PD, Campbell IG, Dunning AM, Le Calvez-Kelm F, Goldgar DE, Tavtigian SV, Chenevix-Trench G. Journal: J Med Genet. 2016 May;53(5):298-309. doi: 10.1136/jmedgenet-2015-103529. Epub 2016 Feb 26.    PubMed
5.	Circular RNAs: a new frontier in the study of human diseases. Author: Chen Y, Li C, Tan C, Liu X. Journal: J Med Genet. 2016 Jun;53(6):359-65. doi: 10.1136/jmedgenet-2016-103758. Epub 2016 Mar 3. Review.    PubMed
6.	AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis. Author: Li W, Li Y, Zhang L, Guo H, Tian D, Li Y, Peng Y, Zheng Y, Dai Y, Xia K, Lan X, Wang B, Hu Z. Journal: J Med Genet. 2016 Jul;53(7):488-93. doi: 10.1136/jmedgenet-2015-103684. Epub 2016 Mar 17.    PubMed
7.	Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity. Author: Iida A, Xing W, Docx MK, Nakashima T, Wang Z, Kimizuka M, Van Hul W, Rating D, Spranger J, Ohashi H, Miyake N, Matsumoto N, Mohan S, Nishimura G, Mortier G, Ikegawa S. Journal: J Med Genet. 2016 Apr 7. pii: jmedgenet-2016-103756. doi: 10.1136/jmedgenet-2016-103756. [Epub ahead of print]    PubMed
8.	The genetic landscape and clinical implications of vertebral anomalies in VACTERL association. Author: Chen Y, Liu Z, Chen J, Zuo Y, Liu S, Chen W, Liu G, Qiu G, Giampietro PF, Wu N, Wu Z. Journal: J Med Genet. 2016 Jul;53(7):431-7. doi: 10.1136/jmedgenet-2015-103554. Epub 2016 Apr 15. Review.    PubMed
9.	A splicing mutation in VPS4B causes dentin dysplasia I. Author: Yang Q, Chen D, Xiong F, Chen D, Liu C, Liu Y, Yu Q, Xiong J, Liu J, Li K, Zhao L, Ye Y, Zhou H, Hu L, Tian Z, Shang X, Zhang L, Wei X, Zhou W, Li D, Zhang W, Xu X. Journal: J Med Genet. 2016 May 31. pii: jmedgenet-2015-103619. doi: 10.1136/jmedgenet-2015-103619. [Epub ahead of print]    PubMed
10.	Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos. Author: Feng R, Yan Z, Li B, Yu M, Sang Q, Tian G, Xu Y, Chen B, Qu R, Sun Z, Sun X, Jin L, He L, Kuang Y, Cowan NJ, Wang L. Journal: J Med Genet. 2016 Jun 6. pii: jmedgenet-2016-103891. doi: 10.1136/jmedgenet-2016-103891. [Epub ahead of print]    PubMed

同类著名期刊名称 h-index CiteScore NATURE REVIEWS GENETICS 320 73.50 NATURE GENETICS 527 45.20 TRENDS IN GENETICS 208 17.20 Annual Review of Genetics 171 16.70 AMERICAN JOURNAL OF HUMAN GENETICS 280 16.90 GENETICS IN MEDICINE 111 12.60 Annual Review of Genomics and Human Genetics 104 12.90 AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS 93 7.60 HUMAN GENETICS 126 9.40 PLoS Genetics 194 9.00

中科院JCR同大类学科的热搜期刊 浏览次数 MEDICINE 301009 CANCER RESEARCH 166233 Molecular Medicine Reports 165047 International Journal of Nanomedicine 164759 CANCER LETTERS 159837 JOURNAL OF ETHNOPHARMACOLOGY 142065 BIOMEDICINE & PHARMACOTHERAPY 141153 Theranostics 136281 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 136236 International Journal of Environmental Research and Public Health 133900