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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

Studying carrier frequency of spinal muscular atrophy in the State of Qatar and comparison to other ethnic groups: Pilot study

Ibrahim, Faisal; Velayutham, Dinesh; Alsharshani, Mohamed; AlAlami, Usama; AlDewik, Manar; Abuarja, Tala; Al Rifai, Hilal; Al‐Dewik, Nader I.

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2184pmid: 37964750

journal article

Open Access Collection

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742‐2A>G

Reinhold, Vivian; Syrjänen, Stina; Kankuri‐Tammilehto, Minna

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2275pmid: 37665136

journal article

Open Access Collection

Congenital central hypoventilation syndrome in Chinese population: Analysis of three new cases and review of the literature

Wang, Yaoyao; Wang, Lina; Chen, Xiaoying; Liu, Shiguo; Han, Wei; Yu, Xinjuan; Cao, Xipeng; Liu, Xiuxiang; Wang, Jiahui

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2267pmid: 37712713

journal article

Open Access Collection

A somatic splice‐site variant in PIK3R1 in a patient with vascular overgrowth and low immunoglobulin levels: A case report

Wilke, Matheus V. M. B.; Schimmenti, Lisa; Lopour, Madeline Q. R.; Tollefson, Megha M.; Klee, Eric W.

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2271pmid: 37641480

journal article

Open Access Collection

Promoter hypermethylation of RARB and GSTP1 genes in plasma cell‐free DNA as breast cancer biomarkers in Peruvian women

Danos, Pierina; Giannoni‐Luza, Stefano; Murillo Carrasco, Alexis Germán; Acosta, Oscar; Guevara‐Fujita, Maria Luisa; Cotrina Concha, José Manuel; Guerra Miller, Henry; Pinto Oblitas, Joseph; Aguilar Cartagena, Alfredo; Araujo, Jhajaira M.; Fujita, Ricardo; Buleje Sono, José Luis

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2260pmid:

journal article

Open Access Collection

Caregiver‐based perception of disease burden in Schaaf‐Yang syndrome

Dötsch, Laura; Matesevac, Lisa; Strong, Theresa V.; Schaaf, Christian P.

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2262pmid: 37533374

journal article

Open Access Collection

A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review

Mir, Atefeh; Song, Yongjun; Lee, Hane; Montazer‐Zohouri, Mostafa; Reisi, Marziyeh; Tabatabaiefar, Mohammad Amin

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2261pmid: 37496384

journal article

Open Access Collection

Clinical report and genetic analysis of a Chinese neonate with craniofacial microsomia caused by a splicing variant of the splicing factor 3b subunit 2 gene

Zhang, Yongli; Bi, Shaohua; Dai, Liying; Zhao, Yuwei; Liu, Yu; Shi, Zifeng

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2268pmid: 37555391

journal article

Open Access Collection

Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population

Ford, Cara P.; Littlejohn, Rebecca O.; German, Ryan; Vuocolo, Blake; Aceves, Jose; Vossaert, Liesbeth; Owen, Nichole; Wangler, Michael; Schmid, Carrie A.; ,

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2272pmid: 37614148

journal article

Open Access Collection

Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review

Zhao, Tianxue; Xu, Shaokun; Liu, Siyue; Xu, Juan; Zhang, Xianfeng; Zhan, Yuhong

2023 Molecular Genetics & Genomic Medicine

doi: 10.1002/mgg3.2276pmid: 37680026

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