Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects
出版年份 2020 全文链接
标题
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects
作者
关键词
Metaanalysis, Genome-wide association studies, Birth defects, Cardiovascular disease risk, Genomics, Single nucleotide polymorphisms, Genome analysis, Oocytes
出版物
PLoS One
Volume 15, Issue 6, Pages e0234357
出版商
Public Library of Science (PLoS)
发表日期
2020-06-10
DOI
10.1371/journal.pone.0234357
参考文献
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect
- (2019) Michelle Kaplinski et al. PLoS One
- Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects
- (2019) Anshuman Sewda et al. PLoS One
- Loss and Rebirth of the Animal Microtubule Organizing Center: How Maternal Expression of Centrosomal Proteins Cooperates with the Sperm Centriole in Zygotic Centrosome Reformation
- (2018) Daigo Inoue et al. BIOESSAYS
- Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles
- (2018) JianHua Qian et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Linker histone H1FOO regulates the chromatin structure in mouse zygotes
- (2018) Satoshi Funaya et al. FEBS LETTERS
- Maternal variants inNLRPand other maternal effect proteins are associated with multilocus imprinting disturbance in offspring
- (2018) Matthias Begemann et al. JOURNAL OF MEDICAL GENETICS
- NLRP genes and their role in preeclampsia and multi-locus imprinting disorders
- (2018) Lukas Soellner et al. JOURNAL OF PERINATAL MEDICINE
- The Congenital Heart Disease Genetic Network Study: Cohort description
- (2018) Thanh T. Hoang et al. PLoS One
- Myosin1D is an evolutionarily conserved regulator of animal left–right asymmetry
- (2018) Thomas Juan et al. Nature Communications
- Formation and dynamics of cytoplasmic domains and their genetic regulation during the zebrafish oocyte-to-embryo transition
- (2018) Ricardo Fuentes et al. MECHANISMS OF DEVELOPMENT
- Dual-spindle formation in zygotes keeps parental genomes apart in early mammalian embryos
- (2018) Judith Reichmann et al. SCIENCE
- Maternal hypertension and hypospadias in offspring: A systematic review and meta-analysis
- (2018) Fatima R. Sheriff et al. Birth Defects Research
- Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming
- (2017) Sangeetha Mahadevan et al. Scientific Reports
- Genome-Wide Association Studies and Meta-Analyses for Congenital Heart DefectsCLINICAL PERSPECTIVE
- (2017) A. J. Agopian et al. Circulation-Cardiovascular Genetics
- Inpatient Hospitalization Costs Associated with Birth Defects Among Persons of All Ages — United States, 2013
- (2017) Annelise C. Arth et al. MMWR-MORBIDITY AND MORTALITY WEEKLY REPORT
- Cardiac Embryology and Molecular Mechanisms of Congenital Heart Disease
- (2016) Benjamin Kloesel et al. ANESTHESIA AND ANALGESIA
- Progress in methods for rare variant association
- (2016) Stephanie A. Santorico et al. BMC GENETICS
- Detection of Allelic Frequency Differences between the Sexes in Humans: A Signature of Sexually Antagonistic Selection
- (2016) Elise A. Lucotte et al. Genome Biology and Evolution
- The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception?
- (2016) Maureen L. Condic Stem Cell Reviews and Reports
- Are hypertensive disorders in pregnancy associated with congenital malformations in offspring? Evidence from the WHO Multicountry cross sectional survey on maternal and newborn health
- (2016) S. Bellizzi et al. BMC Pregnancy and Childbirth
- The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception?
- (2016) Maureen L. Condic Stem Cell Reviews and Reports
- Maternal Hypertension During Pregnancy and the Risk of Congenital Heart Defects in Offspring: A Systematic Review and Meta-analysis
- (2015) Anushuya Ramakrishnan et al. PEDIATRIC CARDIOLOGY
- Maternal control of early embryogenesis in mammals
- (2015) Kun Zhang et al. REPRODUCTION FERTILITY AND DEVELOPMENT
- Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans
- (2015) Louise E. Docherty et al. Nature Communications
- Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations
- (2014) Laura E. Mitchell et al. HUMAN MOLECULAR GENETICS
- Is preeclampsia associated with fetal malformation? A review and report of original research
- (2014) David B. Nelson et al. Journal of Maternal-Fetal & Neonatal Medicine
- DBTMEE: a database of transcriptome in mouse early embryos
- (2014) Sung-Joon Park et al. NUCLEIC ACIDS RESEARCH
- Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects
- (2014) A. J. Agopian et al. PLoS One
- Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants
- (2013) Iuliana Ionita-Laza et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The role of MATER in endoplasmic reticulum distribution and calcium homeostasis in mouse oocytes
- (2013) Boram Kim et al. DEVELOPMENTAL BIOLOGY
- Nongenetic Risk Factors and Congenital Heart Defects
- (2013) Sonali S. Patel et al. PEDIATRIC CARDIOLOGY
- Loss of GGN Leads to Pre-Implantation Embryonic Lethality and Compromised Male Meiotic DNA Double Strand Break Repair in the Mouse
- (2013) Duangporn Jamsai et al. PLoS One
- Diabetes and Obesity-Related Genes and the Risk of Neural Tube Defects in the National Birth Defects Prevention Study
- (2012) P. J. Lupo et al. AMERICAN JOURNAL OF EPIDEMIOLOGY
- Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts
- (2012) Min Shi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
- (2012) Bryan Howie et al. NATURE GENETICS
- Congenital heart defects and maternal genetic, metabolic, and lifestyle factors
- (2011) Charlotte A. Hobbs et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- SLAIN2 links microtubule plus end–tracking proteins and controls microtubule growth in interphase
- (2011) Babet van der Vaart et al. JOURNAL OF CELL BIOLOGY
- GGN1 in the testis and ovary and its variance within the Australian fertile and infertile male population
- (2010) D. Jamsai et al. INTERNATIONAL JOURNAL OF ANDROLOGY
- Conotruncal Cardiac Defects: A Clinical Imaging Perspective
- (2010) Tiffanie R. Johnson PEDIATRIC CARDIOLOGY
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
- (2009) Bryan N. Howie et al. PLoS Genetics
- Shifting Paradigm of Association Studies: Value of Rare Single-Nucleotide Polymorphisms
- (2008) Ivan P. Gorlov et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study
- (2008) Abee L. Boyles et al. GENETIC EPIDEMIOLOGY
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