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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

Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data‐Based Read‐Depth Approach

Fabian‐Morales, Gerardo E.; Ordoñez‐Labastida, Vianey; Garcia‐Martínez, Froylan; Montes‐Almanza, Luis; Zenteno, Juan C.

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70019pmid: 39400524

journal article

Open Access Collection

A Systematic Review Exploring Empirical Pharmacogenomics Research Within Global Indigenous Populations

Nasir, Bushra Farah; Vinayagam, Ritwika; Massi, Luciana; Nagaraj, Shivashankar H.; Toombs, Maree; Rae, Kym M.

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70018pmid: 39435544

journal article

Open Access Collection

Molecular Pathology of Myotonic Dystrophy Type 1 in Iceland

Hallgrímsdóttir, E. G.; Svansson, H.; Stefánsdóttir, V. F.; Sveinsson, Ó. Á.; Ólafsdóttir, H.; Briem, E.; Sveinbjörnsdóttir, S.; Jónsson, J. J.

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70013pmid: 39373365

journal article

Open Access Collection

Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families

Kraoua, Ichraf; Jamoussi, Maha; Drissi, Cyrine; Kraoua, Lilia; Drunat, Séverine; Benrhouma, Hanene; Ben Younes, Thouraya; Nagi, Sonia; Abdelhak, Sonia; Boespflug Tanguy, Odile; Youssef‐Turki, Ilhem Ben; Trabelsi, Mediha; Dorboz, Imen

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70007pmid: 39436788

journal article

Open Access Collection

CANVAR: A Tool for Clinical Annotation of Variants Using ClinVar Databases

Vestergaard, Lau K.; Lopacinska‐Jørgensen, Joanna; Høgdall, Estrid V.

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70020pmid: 39382066

journal article

Open Access Collection

Application of Whole‐Exome Sequencing in the Prenatal Diagnosis of Foetuses With Central Nervous System Abnormalities

Luo, Caiqun; Wen, Erya; Liu, Yang; Wang, Hui; Jia, Bei; Chen, Liyuan; Wu, Xiaoxia; Geng, Qian; Wen, Huaxuan; Li, Shengli; Liu, Bingguang; Wu, Weiqing; Zhong, Mei

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70016pmid: 39359128

journal article

Open Access Collection

Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort

Chung, Clara W. T.; Bournazos, Adam M.; Chan, Lok Chi Denise; Sarkozy, Vanessa; Lawson, John; Kennedy, Sean E.; Cooper, Sandra T.; Kirk, Edwin P.; Mowat, David

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70017pmid: 39352229

journal article

Open Access Collection

Atypical Presentation of Congenital Insensitivity to Pain With Anhidrosis Leading to Diagnostic Odyssey

Higashimoto, Tomoyasu; Garber, Martin E.; Hipp, Lauren; Damon, Jenna; Li, Qing

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70027pmid: 39465509

journal article

Open Access Collection

Extremely Low Birth Weight Infant (Gestational Age of 29 Weeks) With Kabuki Syndrome Type I: Case Report and Literature Review

Li, Qi; Zheng, Yuzhu; Guo, Xinyuan; Xue, Jiang

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.70025pmid: 39400990

journal article

Open Access Collection

Issue Information

2024 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2212pmid: N/A

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