Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis-Reference-Cited by-同舟云学术

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Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis

Published:2017-07-13 Issue:8 Volume:39 Page:1700012
ISSN:0265-9247
Container-title:BioEssays
language:en
Short-container-title:BioEssays

Author:

Beaudet Arthur L.¹

Affiliation:

1. Departments of Molecular and Human Genetics and Pediatrics; Baylor College of Medicine; Texas Children's Hospital; Houston TX USA

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

The William Stamps Farish Fund

Simons Foundation

Autism Speaks

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

Reference110 articles.

1. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism;Celestino-Soper;Proc Natl Acad Sci USA,2012

2. Identifying autism susceptibility genes;Maestrini;Neuron,2000

3. A genomic screen of autism: evidence for a multilocus etiology;Risch;Am J Hum Genet,1999

4. Strong association of de novo copy number mutations with autism;Sebat;Science,2007

5. The contribution of de novo coding mutations to autism spectrum disorder;Iossifov;Nature,2014

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2. Donor-recipient intermicrobial interactions impact transfer of subspecies and fecal microbiota transplantation outcome;Cell Host & Microbe;2024-03

3. Corn gluten meal diets supplemented with dietary L-carnitine for juvenile hybrid grouper (♀Epinephelus fuscoguttatus × ♂E. lanceolatus): Impacts on growth performance, immune response and flesh quality;Animal Feed Science and Technology;2024-02

4. Unraveling the metabolomic architecture of autism in a large Danish population-based cohort;2023-11-30

5. Metabolomic biomarkers in autism: identification of complex dysregulations of cellular bioenergetics;Frontiers in Psychiatry;2023-10-02

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