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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:
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

Clinical Features and PLCZ1 Gene Variants in Two Cases of Male Infertility: A Case Series and Literature Review

Yang, Jinwei; Yan, Bo; Wei, Zhizhuo; Niu, Zijing; Wang, Tongguang; Wei, Yan; Wang, Fangzhu; Jiang, Wei; Zhang, Lin; Da, Yue; Wang, Huanjing; Ni, Yali; Wang, Zhiqiang

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70250pmid: N/A

journal article

Open Access Collection

MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia

Kalayinia, Samira; Masoumi, Tannaz; Taherkhani, Amirreza; Mahdieh, Nejat; Khorgami, Mohammadrafie; Maleki, Majid

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70244pmid: N/A

journal article

Open Access Collection

Association of a Homozygous TYMP c.131G>C Variant With MNGIE in a Chinese Pedigree: Insights From Genetic Analysis and Computational Modeling

Li, Ling; Chen, Xiu; Li, Hua; Guo, Kai; Zhang, Ting; Ma, Mingyi; Zhao, Songhua

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70253pmid: N/A

journal article

Open Access Collection

Genetic Analysis of Pitt–Hopkins Syndrome Caused by a Novel Splicing Variant (c.1146+3A>T) in the TCF4 Gene

Shen, Wenlong; Zhang, Yan; Wu, Junjie; Zhao, Jue; Lv, Yaer; Tang, Xiaohua

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70239pmid: N/A

journal article

Open Access Collection

X‐Linked Intellectual Developmental Disorder‐93 Caused by BRWD3 Mutation in Females: A Case Report and Literature Review

Xiu, Yang; Zhang, Yige; Jiao, Yake; Wang, Wei; Hu, Yanyan

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70251pmid: N/A

journal article

Open Access Collection

Differential Transcriptome Analysis of Intrauterine UPD6pat Fetuses With Distinct Phenotypes

Yu, Jiahui; Zhang, Yan; Shen, Wenlong; Ying, Jun; Li, Huanzheng; Tang, Xiaohua; He, Xujun

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70241pmid: N/A

journal article

Open Access Collection

Correction to “Identification and Functional Analysis of a Novel NSD2 Missense Variant in a Patient With Rauch‐Steindl Syndrome”

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70252pmid: 42289922

journal article

Open Access Collection

A Novel Approach to Interrogating Whole Genome Sequencing Data to Optimise Clinical Utility

Sonner, Sarah; McKenna, Caoimhe; Heggarty, Shirley; Hamill, Cassie; Flanagan, Cheryl; McKee, Shane; Kerr, Katie; Alhazzaa, Rasha; McKnight, Amy Jayne; Mone, Fionnuala

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70248pmid: N/A

journal article

Open Access Collection

A Case Report of Shwachman‐Diamond Syndrome Caused by Heterozygous Variants in the EFL1 Gene and Literature Review

Zhou, Xiaoying; Li, Hongxin; Yang, Xinyi; Wang, Chunli; Zhang, Wenting

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70249pmid: N/A

journal article

Open Access Collection

A Rare Clinical Presentation of Variegate Porphyria

Viakhireva, I.; Murtazina, A.; Orlova, A.; Makretskaya, N.; Nikitin, S.; Skoblov, M.

2026 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70243pmid: N/A

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