molecular genetics & genomic medicine

Rank: 18.42 /
Indexings
ncbi ulakbim MEP: - Ödeme: 3750 Yılı: 2019
Short Name mol genet genomic med
Abbreviated Name mol genet genomic med
ISSN 2324-9269
Aim and Scope
URL
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Publications Per Year

Top 10 Most Clicked Articles

2019 Zhang, Ziyang, Tang, Dongyang, Wang, Bin, Wang, Zhiwei, Liu, Mingjiu,

Analysis of miRNA-mRNA regulatory network revealed key genes induced by aflatoxin B1 exposure in primary human hepatocytes. ,

Vol N/A: e971
Clicks: 319
2019 Chan, Melody Lok-Yi, Cheung, Ching-Lung, Lee, Alan Chun-Hong, Yeung, Chun-Yip, Siu, Chung-Wah, Leung, Jenny Yin-Yan, Pang, Ho-Kwong, Tan, Kathryn Choon-Beng,

Genetic variations in familial hypercholesterolemia and cascade screening in East Asians. ,

7: e00520
Clicks: 295
2019 Biag, Hazel Maridith B, Potter, Laura A, Wilkins, Victoria, Afzal, Sumra, Rosvall, Alexis, Salcedo-Arellano, Maria Jimena, Rajaratnam, Akash, Manzano-Nunez, Ramiro, Schneider, Andrea, Tassone, Flora, Rivera, Susan M, Hagerman, Randi J,

Metformin treatment in young children with fragile X syndrome. ,

Vol N/A: e956
Clicks: 248
2019 Keicho, Naoto, Hijikata, Minako, Morimoto, Kozo, Homma, Sakae, Taguchi, Yoshio, Azuma, Arata, Kudoh, Shoji,

Primary ciliary dyskinesia caused by a large homozygous deletion including exons 1-4 of DRC1 in Japanese patients with recurrent sinopulmonary infection. ,

Vol N/A: e1033
Clicks: 231
2019 Barboza-Cerda, María Carmen, Barboza-Quintana, Oralia, Martínez-Aldape, Gerardo, Garza-Guajardo, Raquel, Déctor, Miguel Angel,

Phenotypic severity in a family with MEND syndrome is directly associated with the accumulation of potentially functional variants of cholesterol homeostasis genes. ,

Vol N/A: e931
Clicks: 229
2019 Zhang, Hong, Hu, Yuanyuan, Seymen, Figen, Koruyucu, Mine, Kasimoglu, Yelda, Wang, Shih-Kai, Wright, John Timothy, Havel, Michael W, Zhang, Chuhua, Kim, Jung-Wook, Simmer, James P, Hu, Jan C-C,

ENAM mutations and digenic inheritance. ,

Vol N/A: e928
Clicks: 214
2019 Chai, Hongyan, Grommisch, Brittany, DiAdamo, Autumn, Wen, Jiadi, Hui, Pei, Li, Peining,

Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion. ,

Vol N/A: e965
Clicks: 211
2020 Santos, Ellery, Emeka-Nwonovo, Chinelo, Wang, Jun Yi, Schneider, Andrea, Tassone, Flora, Hagerman, Paul, Hagerman, Randi,

Developmental aspects of FXAND in a man with the FMR1 premutation. ,

Vol N/A: e1050
Clicks: 198
2019 Xiao, Bing, Wang, Lili, Liu, Huili, Fan, Yanjie, Xu, Yan, Sun, Yu, Qiu, Wenjuan,

Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosity. ,

Vol N/A: e945
Clicks: 189
2018 Reinders, Marie G, van Hout, Antonius F, Cosgun, Betûl, Paulussen, Aimée D, Leter, Edward M, Steijlen, Peter M, Mosterd, Klara, van Geel, Michel, Gille, Johan J,

New mutations and an updated database for the patched-1 (PTCH1) gene. ,

6: 409-415
Clicks: 164

Certificate of Indexing

This is to certify that

molecular genetics & genomic medicine

ISSN: 2324-9269

is being indexed by Journament

Indexing started on: August 28, 2019
Certificate issued on: July 29, 2025
Verification link: https://journament.com/journal_stat/5330

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