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New Evidence against Chromium as an Essential Trace Element

The Journal of nutrition, 2017-12, Vol.147 (12), p.2212-2219

Vincent, John B

2017

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Chromium: celebrating 50 years as an essential element?

Dalton transactions : an international journal of inorganic chemistry, 2010-01, Vol.39 (16), p.3787-3794

Vincent, John B

2010

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Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles

Current biology, 2015-08, Vol.25 (17), p.2278-2283

2015

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MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

Frontiers in genetics, 2021-01, Vol.12, p.620859-620859

2021

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Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.856-863

2012

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Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

American journal of human genetics, 2016-10, Vol.99 (4), p.912-916

2016

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Effects of chromium supplementation on body composition, human and animal health, and insulin and glucose metabolism

Current opinion in clinical nutrition and metabolic care, 2019-11, Vol.22 (6), p.483-489

Vincent, John B.

2019

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Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder

Scientific reports, 2024-04, Vol.14 (1), p.9230-9230, Article 9230

2024

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Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment

Molecular ecology, 2016-08, Vol.25 (16), p.4032-4046

2016

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The genetic basis of non-syndromic intellectual disability: a review

Journal of neurodevelopmental disorders, 2010-12, Vol.2 (4), p.182-209

2010

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The Bioinorganic Chemistry of Chromium

Vincent, John

1. Aufl., 2012

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The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual Disability

Cold Spring Harbor perspectives in medicine, 2017-03, Vol.7 (3), p.a026864

2017

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Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe

Ecological applications, 2017-04, Vol.27 (3), p.756-768

2017

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Neuronal transcription of autism gene PTCHD1 is regulated by a conserved downstream enhancer sequence

Scientific reports, 2023-11, Vol.13 (1), p.20391-20391, Article 20391

2023

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What Are the Implications of Cr(III) Serving as an Inhibitor of the Beta Subunit of Mitochondrial ATP Synthase?

Biological trace element research, 2024-04, Vol.202 (4), p.1335-1344

Vincent, John B.

2024

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Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2014-12, Vol.95 (6), p.721-728

2014

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Is chromium(III) pharmacologically relevant? An update focused on studies with diabetic rodent models

Journal of trace elements in medicine and biology, 2024-07, Vol.84, p.127453-127453, Article 127453

Vincent, John B.

2024

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Is chromium(III) supplementation beneficial for dietary rodent models of prediabetes?

Journal of trace elements in medicine and biology, 2024-09, Vol.85, p.127482, Article 127482

Vincent, John B.

2024

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Recent advances in the nutritional biochemistry of trivalent chromium

Proceedings of the Nutrition Society, 2004-02, Vol.63 (1), p.41-47

Vincent, John B

2004

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A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

Human molecular genetics, 2014-11, Vol.23 (22), p.5940-5949

2014

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Is the Pharmacological Mode of Action of Chromium(III) as a Second Messenger?

Biological trace element research, 2015-07, Vol.166 (1), p.7-12

Vincent, John B

2015

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A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain

Journal of human genetics, 2020-05, Vol.65 (5), p.493-496

2020

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Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14

Scientific reports, 2021-11, Vol.11 (1), p.23113-11, Article 23113

2021

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Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families

Neurogenetics, 2014-05, Vol.15 (2), p.117-127

2014

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Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2011-07, Vol.89 (1), p.176-182

2011

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New Evidence against Chromium as an Essential Trace Element

Chromium: celebrating 50 years as an essential element?

Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

Effects of chromium supplementation on body composition, human and animal health, and insulin and glucose metabolism

Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder

Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment

The genetic basis of non-syndromic intellectual disability: a review

The Bioinorganic Chemistry of Chromium

The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual Disability

Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe

Neuronal transcription of autism gene PTCHD1 is regulated by a conserved downstream enhancer sequence

What Are the Implications of Cr(III) Serving as an Inhibitor of the Beta Subunit of Mitochondrial ATP Synthase?

Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

Is chromium(III) pharmacologically relevant? An update focused on studies with diabetic rodent models

Is chromium(III) supplementation beneficial for dietary rodent models of prediabetes?

Recent advances in the nutritional biochemistry of trivalent chromium

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

Is the Pharmacological Mode of Action of Chromium(III) as a Second Messenger?

A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain

Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

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