GENETICS IN MEDICINE

生物 遗传学

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  • 中科院分区:医学 1区[Top] 医学 1 区
  • 审稿周期:平均1月
  • 自引率:15.3%
  • 录取率:25.%
  • ISSN:2190-572X
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  • 年文章数:454
  • 国人占比:5.42%
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期刊简介

3 BIOTECH杂志暂不明确行业,暂不明确子行业的级别不明杂志

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杂志水平一般,也很冷门,关注人少,审稿周期可能也不一定快,如果文章质量不佳,或时间不紧的话,可以考虑考虑。

Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid features.

DOI:10.1016/j.gim.2022.05.004

发表时间:2022 Jun 6

作者:Kornak U;Saha N;Keren B;Neumann A;Taylor Tavares AL;Piard J;Kopp J;Rodrigues Alves JG;Rodríguez de Los Santos M;El Choubassi N;Ehmke N;Jäger M;Spielmann M;Pantel JT;Lejeune E;Fauler B;Mielke T;Hecht J;Meierhofer D;Strom TM;Laugel V;Brice A;Mundlos S;Bertoli-Avella A;Bauer P;Heyd F;Boute O;Dupont J;Depienne C;Van Maldergem L;Fischer-Zirnsak B

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation.

DOI:10.1016/j.gim.2022.05.007

发表时间:2022 Jun 8

作者:Plotkin SR;Messiaen L;Legius E;Pancza P;Avery RA;Blakeley JO;Babovic-Vuksanovic D;Ferner R;Fisher MJ;Friedman JM;Giovannini M;Gutmann DH;Hanemann CO;Kalamarides M;Kehrer-Sawatzki H;Korf BR;Mautner VF;MacCollin M;Papi L;Rauen KA;Riccardi V;Schorry E;Smith MJ;Stemmer-Rachamimov A;Stevenson DA;Ullrich NJ;Viskochil D;Wimmer K;Yohay K;International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC).;Huson SM;Wolkenstein P;Evans DG

Rare pathogenic variants in WNK3 cause X-linked intellectual disability.

DOI:10.1016/j.gim.2022.05.009

发表时间:2022 Jun 9

作者:Küry S;Zhang J;Besnard T;Caro-Llopis A;Zeng X;Robert SM;Josiah SS;Kiziltug E;Denommé-Pichon AS;Cogné B;Kundishora AJ;Hao LT;Li H;Stevenson RE;Louie RJ;Deb W;Torti E;Vignard V;McWalter K;Raymond FL;Rajabi F;Ranza E;Grozeva D;Coury SA;Blanc X;Brischoux-Boucher E;Keren B;Õunap K;Reinson K;Ilves P;Wentzensen IM;Barr EE;Guihard SH;Charles P;Seaby EG;Monaghan KG;Rio M;van Bever Y;van Slegtenhorst M;Chung WK;Wilson A;Quinquis D;Bréhéret F;Retterer K;Lindenbaum P;Scalais E;Rhodes L;Stouffs K;Pereira EM;Berger SM;Milla SS;Jaykumar AB;Cobb MH;Panchagnula S;Duy PQ;Vincent M;Mercier S;Gilbert-Dussardier B;Le Guillou X;Audebert-Bellanger S;Odent S;Schmitt S;Boisseau P;Bonneau D;Toutain A;Colin E;Pasquier L;Redon R;Bouman A;Rosenfeld JA;Friez MJ;Pérez-Peña H;Akhtar Rizvi SR;Haider S;Antonarakis SE;Schwartz CE;Martínez F;Bézieau S;Kahle KT;Isidor B

Detection and characterization of male sex chromosome abnormalities in the UK Biobank study.

DOI:10.1016/j.gim.2022.05.011

发表时间:2022 Jun 9

作者:Zhao Y;Gardner EJ;Tuke MA;Zhang H;Pietzner M;Koprulu M;Jia RY;Ruth KS;Wood AR;Beaumont RN;Tyrrell J;Jones SE;Lango Allen H;Day FR;Langenberg C;Frayling TM;Weedon MN;Perry JRB;Ong KK;Murray A

Development and evaluation of polygenic risk scores for prediction of endometrial cancer risk in European women.

DOI:10.1016/j.gim.2022.05.014

发表时间:2022 Jun 15

作者:Bafligil C;Thompson DJ;Lophatananon A;Ryan NAJ;Smith MJ;Dennis J;Mekli K;O'Mara TA;Evans DG;Crosbie EJ

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