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Molecular Genetics & Genomic Medicine | DeepDyve

Molecular Genetics & Genomic Medicine

Subject:: Genetics
Publisher:: Wiley Subscription Services, Inc., A Wiley Company — Wiley
ISSN:: 2324-9269
Scimago Journal Rank:: 34

2026

Volume 14

Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2025

Volume 13

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)

2024

Volume 12

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2023

Volume 11

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2022

Volume 10

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2021

Volume 9

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2020

Volume 8

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2019

Volume 7

Issue 12 (Dec)Issue 11 (Nov)Issue 10 (Oct)Issue 9 (Sep)Issue 8 (Aug)Issue 7 (Jul)Issue 6 (Jun)Issue 5 (May)Issue 4 (Apr)Issue 3 (Mar)Issue 2 (Feb)Issue 1 (Jan)

2018

Volume 6

Issue 6 (Jan)Issue 5 (Jan)Issue 4 (Jan)Issue 3 (Jan)Issue 2 (Jan)Issue 1 (Jan)

2017

Volume 5

Issue 6 (Jan)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2016

Volume 4

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2015

Volume 3

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2014

Volume 2

Issue 6 (Nov)Issue 5 (Sep)Issue 4 (Jul)Issue 3 (May)Issue 2 (Mar)Issue 1 (Jan)

2013

Volume 1

Issue 4 (Nov)Issue 3 (Sep)Issue 2 (Jul)Issue 1 (May)

journal article

Open Access Collection

Correction to “In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome”

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2487pmid: 39001575

journal article

Open Access Collection

Glucose‐6‐phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review

Iyer, Neel S.; Mossayebi, Matthew H.; Gao, Tracy J.; Haizler‐Cohen, Lylach; Di Mascio, Daniele; McLaren, Rodney A.; Al‐Kouatly, Huda B.

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2491pmid: 39041728

journal article

Open Access Collection

A novel variant in the FLCN gene in a Chinese family with Birt–Hogg–Dubé syndrome

Miao, He; Zhou, Yulin; Ge, Silun; Gu, Yufeng; Qu, Le; Zhou, Wenquan; He, Haowei

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2488pmid: 38963008

journal article

Open Access Collection

Synonymous variant at the terminal nucleotide in exon 3 of F7 causes abnormal splicing: A case report

Wang, Liya; Zeng, Wenshan; Qian, Yeqing; Sun, Yixi; Chen, Min; Liu, Bei; Hu, Junjie; Yu, Ping; Dong, Minyue

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2492pmid: 39007454

journal article

Open Access Collection

A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non‐syndromic deafness 2A in a Chinese family

Ren, Lingyan; Wu, Jiangfen; Kuang, Ying; Chen, Kun; Jiang, Minmin; Zhuo, Zhaozhen; Cao, Zuwei; Huang, Shengwen

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2446pmid: 38980994

journal article

Open Access Collection

Targeted next‐generation sequencing reveals the genetic mechanism of Chinese Marfan syndrome cohort with ocular manifestation

Han, Dongming; Wang, Ziwei; Chen, Xuan; Liu, Zijia; Yang, Zhengtao; Chen, Yixi; Tian, Peiyi; Li, Jiankang; Wang, ZhuoShi

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2482pmid: 38958168

journal article

Open Access Collection

Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay

Chamova, Teodora; Ivanova, Neviana; Cherninkova, Sylvia; Koleva, Maya; Zlatareva, Dora; Bojinova, Veneta; Mihova, Kalina; Georgiev, Martin; Ferdinandov, Dilyan; Bichev, Stoyan; Kaneva, Radka; Mitev, Vanio; Jordanova, Albena; Tournev, Ivailo

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2483pmid: 39044368

journal article

Open Access Collection

Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis

Lee, Chung‐Lin; Chang, Yeun‐Wen; Lin, Hsiang‐Yu; Lee, Hung‐Chang; Yeh, Ting‐Chi; Fang, Li‐Ching; Lee, Ni‐Chung; Tsai, Jeng‐Daw; Lin, Shuan‐Pei

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2494pmid: 39056574

journal article

Open Access Collection

A case of inherited glycosylphosphatidylinositol deficiency caused by PGAP3 variant with uniparental isodisomy on chromosome 17

Mukai, Takeo; Kato, Shota; Tanaka, Hiroyuki; Kuroda, Yukiko; Kitaoka, Hiroki; Ito, Atsushi; Shitara, Yoshihiko; Kashima, Kohei; Takami, Hirokazu; Takahashi, Naoto; Kato, Motohiro

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2452pmid: 38967264

journal article

Open Access Collection

A compound heterozygote case of glutaric aciduria type II in a patient carrying a novel candidate variant in ETFDH gene: A case report and literature review on compound heterozygote cases

Seyedtaghia, Mohammad Reza; Jafarzadeh‐Esfehani, Reza; Hosseini, Seyedmojtaba; Kobravi, Sepehr; Hakkaki, Mahdis; Nilipour, Yalda

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2489pmid: 38967380

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