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Model-based analysis of costs and outcomes of non-invasive prenatal testing for Down's syndrome using cell free fetal DNA in the UK National Health Service

PloS one, 2014-04, Vol.9 (4), p.e93559-e93559

2014

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Efficient Generation of Myostatin Knock-Out Sheep Using CRISPR/Cas9 Technology and Microinjection into Zygotes

PloS one, 2015-08, Vol.10 (8), p.e0136690-e0136690

2015

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iNitro-Tyr: prediction of nitrotyrosine sites in proteins with general pseudo amino acid composition

PloS one, 2014-08, Vol.9 (8), p.e105018-e105018

2014

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Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency

Trends in endocrinology and metabolism, 2018-06, Vol.29 (6), p.400-419

2018

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Gene balance hypothesis: Connecting issues of dosage sensitivity across biological disciplines

Proceedings of the National Academy of Sciences - PNAS, 2012-09, Vol.109 (37), p.14746-14753

2012

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Emerging links between phase separation and transcription factor haploinsufficiency

Trends in genetics, 2024-10

Veitia, Reiner A.

2024

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Association of brain-derived neurotrophic factor gene Val66Met polymorphism with primary dysmenorrhea

PloS one, 2014-11, Vol.9 (11), p.e112766-e112766

2014

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Dominant negative variants and cotranslational assembly of macromolecular complexes

BioEssays, 2023-11, Vol.45 (11), p.e2300105-e2300105

Veitia, Reiner A

2023

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Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2

PloS one, 2013-06, Vol.8 (6), p.e65550-e65550

2013

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Forkhead Transcription Factors in Health and Disease

Trends in genetics, 2021-05, Vol.37 (5), p.460-475

2021

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Visible light photoredox organocatalysis: a fully transition metal-free direct asymmetric α-alkylation of aldehydes

Green chemistry : an international journal and green chemistry resource : GC, 2012-01, Vol.14 (5), p.1293-1297

2012

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Digital PCR validates 8q dosage as prognostic tool in uveal melanoma

PloS one, 2015-03, Vol.10 (3), p.e0116371-e0116371

2015

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bHLH003, bHLH013 and bHLH017 are new targets of JAZ repressors negatively regulating JA responses

PloS one, 2014-01, Vol.9 (1), p.e86182-e86182

2014

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Mechanisms of Mendelian dominance

Clinical genetics, 2018-03, Vol.93 (3), p.419-428

2018

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Who ever thought genetic mutations were random?

Trends in plant science, 2022-08, Vol.27 (8), p.733-735

Veitia, Reiner A.

2022

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The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival

PloS one, 2014-06, Vol.9 (6), p.e100516

2014

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Use of targeted exome sequencing in genetic diagnosis of Chinese familial hypercholesterolemia

PloS one, 2014-04, Vol.9 (4), p.e94697-e94697

2014

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Heterosis

The Plant cell, 2010-07, Vol.22 (7), p.2105-2112

2010

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DNA Content, Cell Size, and Cell Senescence

Trends in biochemical sciences (Amsterdam. Regular ed.), 2019-08, Vol.44 (8), p.645-647

Veitia, Reiner A.

2019

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A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Clinical genetics, 2016-05, Vol.89 (5), p.603-607

2016

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Primary ovarian insufficiency, meiosis and DNA repair

Biomedical Journal, 2020-04, Vol.43 (2), p.115-123

Veitia, Reiner A.

2020

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gene balance hypothesis: implications for gene regulation, quantitative traits and evolution

The New phytologist, 2010-04, Vol.186 (1), p.54-62

2010

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Forkhead transcription factors: key players in health and disease

Trends in genetics, 2011-06, Vol.27 (6), p.224-232

2011

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Transcription factors: specific DNA binding and specific gene regulation

Trends in genetics, 2014-06, Vol.30 (6), p.211-219

2014

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Exploring the etiology of haploinsufficiency

BioEssays, 2002-02, Vol.24 (2), p.175-184

Veitia, Reiner A.

2002

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Model-based analysis of costs and outcomes of non-invasive prenatal testing for Down's syndrome using cell free fetal DNA in the UK National Health Service

Efficient Generation of Myostatin Knock-Out Sheep Using CRISPR/Cas9 Technology and Microinjection into Zygotes

iNitro-Tyr: prediction of nitrotyrosine sites in proteins with general pseudo amino acid composition

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency

Gene balance hypothesis: Connecting issues of dosage sensitivity across biological disciplines

Emerging links between phase separation and transcription factor haploinsufficiency

Association of brain-derived neurotrophic factor gene Val66Met polymorphism with primary dysmenorrhea

Dominant negative variants and cotranslational assembly of macromolecular complexes

Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2

Forkhead Transcription Factors in Health and Disease

Visible light photoredox organocatalysis: a fully transition metal-free direct asymmetric α-alkylation of aldehydes

Digital PCR validates 8q dosage as prognostic tool in uveal melanoma

bHLH003, bHLH013 and bHLH017 are new targets of JAZ repressors negatively regulating JA responses

Mechanisms of Mendelian dominance

Who ever thought genetic mutations were random?

The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival

Use of targeted exome sequencing in genetic diagnosis of Chinese familial hypercholesterolemia

Heterosis

DNA Content, Cell Size, and Cell Senescence

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Primary ovarian insufficiency, meiosis and DNA repair

gene balance hypothesis: implications for gene regulation, quantitative traits and evolution

Forkhead transcription factors: key players in health and disease

Transcription factors: specific DNA binding and specific gene regulation

Exploring the etiology of haploinsufficiency

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