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Etiology and clinical presentation of birth defects: population based study

BMJ (Online), 2017-05, Vol.357, p.j2249

2017

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Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study

BMJ open, 2019-07, Vol.9 (7), p.e028139-e028139

2019

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Associations between maternal periconceptional exposure to secondhand tobacco smoke and major birth defects

American journal of obstetrics and gynecology, 2016-11, Vol.215 (5), p.613.e1-613.e11

2016

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Preventing birth defects, saving lives, and promoting health equity: an urgent call to action for universal mandatory food fortification with folic acid

The Lancet global health, 2022-07, Vol.10 (7), p.e1053-e1057

2022

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Laterality defects in the national birth defects prevention study (1998-2007): Birth prevalence and descriptive epidemiology

American journal of medical genetics. Part A, 2014-10, Vol.164A (10), p.2581-2591

2014

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Diabetes mellitus and birth defects

American journal of obstetrics and gynecology, 2008-09, Vol.199 (3), p.237.e1-237.e9

2008

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International Undiagnosed Diseases Programs (UDPs): components and outcomes

Orphanet journal of rare diseases, 2023-11, Vol.18 (1), p.1-348, Article 348

2023

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Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies

Birth defects research. A Clinical and molecular teratology, 2007-10, Vol.79 (10), p.714-727

2007

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Cancer risk in children and adolescents with birth defects: a population-based cohort study

PloS one, 2013-07, Vol.8 (7), p.e69077-e69077

2013

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The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study

Pediatric cardiology, 2011-12, Vol.32 (8), p.1147-1157

2011

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Turner Syndrome in Girls Presenting with Coarctation of the Aorta

The Journal of pediatrics, 2015-11, Vol.167 (5), p.1062-1066

2015

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Treatment of Hyperthyroidism in Pregnancy and Birth Defects

The journal of clinical endocrinology and metabolism, 2010-11, Vol.95 (11), p.E337-E341

2010

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Improvement in stroke mortality in Canada and the United States, 1990 to 2002

Circulation (New York, N.Y.), 2006-03, Vol.113 (10), p.1335-1343

2006

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Benefits of tailored disease management in improving tremor, white matter hyperintensities, and liver enzymes in a child with heterozygous X-linked ornithine transcarbamylase deficiency

Molecular genetics and metabolism reports, 2022-12, Vol.33 (Suppl 1), p.100891-100891, Article 100891

2022

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Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy

Annals of neurology, 2022-11, Vol.92 (5), p.895-901

2022

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Action against birth defects: if not now, when?

Global health action, 2024-12, Vol.17 (1), p.2354002

2024

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Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling

American journal of human genetics, 2016-08, Vol.99 (2), p.299-317

2016

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MADD-like pattern of acylcarnitines associated with sertraline use

Molecular genetics and metabolism reports, 2024-12, Vol.41, p.101142, Article 101142

2024

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Expanding the genetic and clinical spectrum of the NONO‐associated X‐linked intellectual disability syndrome

American journal of medical genetics. Part A, 2019-05, Vol.179 (5), p.792-796

2019

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Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway

eLife, 2022-09, Vol.11

2022

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Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

PLoS genetics, 2021-03, Vol.17 (3), p.e1009413

2021

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Maternal Exposure to Nitrogen Dioxide, Intake of Methyl Nutrients, and Congenital Heart Defects in Offspring

American journal of epidemiology, 2017-09, Vol.186 (6), p.719-729

2017

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Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 years

BMJ open, 2019-09, Vol.9 (9), p.e026351-e026351

2019

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Lack of periconceptional vitamins or supplements that contain folic acid and diabetes mellitus–associated birth defects

American journal of obstetrics and gynecology, 2012-03, Vol.206 (3), p.218.e1-218.e13

2012

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Public Health Approach to Improve Outcomes for Congenital Heart Disease Across the Life Span

Journal of the American Heart Association, 2019-04, Vol.8 (8), p.e009450-e009450

2019

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Etiology and clinical presentation of birth defects: population based study

Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study

Associations between maternal periconceptional exposure to secondhand tobacco smoke and major birth defects

Preventing birth defects, saving lives, and promoting health equity: an urgent call to action for universal mandatory food fortification with folic acid

Laterality defects in the national birth defects prevention study (1998-2007): Birth prevalence and descriptive epidemiology

Diabetes mellitus and birth defects

International Undiagnosed Diseases Programs (UDPs): components and outcomes

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies

Cancer risk in children and adolescents with birth defects: a population-based cohort study

The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study

Turner Syndrome in Girls Presenting with Coarctation of the Aorta

Treatment of Hyperthyroidism in Pregnancy and Birth Defects

Improvement in stroke mortality in Canada and the United States, 1990 to 2002

Benefits of tailored disease management in improving tremor, white matter hyperintensities, and liver enzymes in a child with heterozygous X-linked ornithine transcarbamylase deficiency

Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy

Action against birth defects: if not now, when?

Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling

MADD-like pattern of acylcarnitines associated with sertraline use

Expanding the genetic and clinical spectrum of the NONO‐associated X‐linked intellectual disability syndrome

Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

Maternal Exposure to Nitrogen Dioxide, Intake of Methyl Nutrients, and Congenital Heart Defects in Offspring

Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 years

Lack of periconceptional vitamins or supplements that contain folic acid and diabetes mellitus–associated birth defects

Public Health Approach to Improve Outcomes for Congenital Heart Disease Across the Life Span

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