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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum

Clinical genetics, 2015-10, Vol.88 (4), p.327-335

2015

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Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin

European journal of paediatric neurology, 2018-01, Vol.22 (1), p.93-101

2018

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SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

Neurology, 2009-05, Vol.72 (20), p.1755-1759

2009

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Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy

Journal of medical genetics, 2010-09, Vol.47 (9), p.601-607

2010

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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

Cell, 2019-08, Vol.178 (4), p.850-866.e26

2019

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A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation

Neuron (Cambridge, Mass.), 2019-09, Vol.103 (5), p.785-801.e8

2019

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Let-7 family of microRNA is required for maturation and adult-like metabolism in stem cell-derived cardiomyocytes

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (21), p.E2785-E2794

2015

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KRAS codon 61, 146 and BRAF mutations predict resistance to cetuximab plus irinotecan in KRAS codon 12 and 13 wild-type metastatic colorectal cancer

British journal of cancer, 2009-08, Vol.101 (4), p.715-721

2009

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The identification and functional annotation of RNA structures conserved in vertebrates

Genome research, 2017-08, Vol.27 (8), p.1371-1383

2017

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Model-based clustering and data transformations for gene expression data

Bioinformatics, 2001-10, Vol.17 (10), p.977-987

2001

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A Glycine-Dependent Riboswitch That Uses Cooperative Binding to Control Gene Expression

Science (American Association for the Advancement of Science), 2004-10, Vol.306 (5694), p.275-279

2004

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Genetic epilepsy with febrile seizures plus: Refining the spectrum

Neurology, 2017-09, Vol.89 (12), p.1210-1219

2017

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Identification of 22 candidate structured RNAs in bacteria using the CMfinder comparative genomics pipeline

Nucleic acids research, 2007-07, Vol.35 (14), p.4809-4819

2007

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Chromatin and Transcriptional Analysis of Mesoderm Progenitor Cells Identifies HOPX as a Regulator of Primitive Hematopoiesis

Cell reports (Cambridge), 2017-08, Vol.20 (7), p.1597-1608

2017

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Inhibition of β-catenin signaling respecifies anterior-like endothelium into beating human cardiomyocytes

Development (Cambridge), 2015-09, Vol.142 (18), p.3198-3209

2015

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Associating transcription factors and conserved RNA structures with gene regulation in the human brain

Scientific reports, 2017-07, Vol.7 (1), p.5776-16, Article 5776

2017

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6S RNA is a widespread regulator of eubacterial RNA polymerase that resembles an open promoter

RNA (Cambridge), 2005-05, Vol.11 (5), p.774-784

2005

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Identification and characterization of novel conserved RNA structures in Drosophila

BMC genomics, 2018-12, Vol.19 (1), p.899-899, Article 899

2018

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Glycolysis gene expression analysis and selective metabolic advantage in the clinical progression of colorectal cancer

The pharmacogenomics journal, 2017-06, Vol.17 (3), p.258-264

2017

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Dihydropyrimidine dehydrogenase pharmacogenetics for predicting fluoropyrimidine-related toxicity in the randomised, phase III adjuvant TOSCA trial in high-risk colon cancer patients

British journal of cancer, 2017-10, Vol.117 (9), p.1269-1277

2017

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Does rapid sequence divergence preclude RNA structure conservation in vertebrates?

Nucleic acids research, 2022-03, Vol.50 (5), p.2452-2463

2022

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widespread riboswitch candidate that controls bacterial genes involved in molybdenum cofactor and tungsten cofactor metabolism

Molecular microbiology, 2008-05, Vol.68 (4), p.918-932

2008

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Sexual ancestors generated an obligate asexual and globally dispersed clone within the model diatom species Thalassiosira pseudonana

Scientific reports, 2018-07, Vol.8 (1), p.10492-9, Article 10492

2018

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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy

Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation

Let-7 family of microRNA is required for maturation and adult-like metabolism in stem cell-derived cardiomyocytes

KRAS codon 61, 146 and BRAF mutations predict resistance to cetuximab plus irinotecan in KRAS codon 12 and 13 wild-type metastatic colorectal cancer

The identification and functional annotation of RNA structures conserved in vertebrates

Model-based clustering and data transformations for gene expression data

Targeting wild-type KRAS-amplified gastroesophageal cancer through combined MEK and SHP2 inhibition

A Glycine-Dependent Riboswitch That Uses Cooperative Binding to Control Gene Expression

Genetic epilepsy with febrile seizures plus: Refining the spectrum

Identification of 22 candidate structured RNAs in bacteria using the CMfinder comparative genomics pipeline

Chromatin and Transcriptional Analysis of Mesoderm Progenitor Cells Identifies HOPX as a Regulator of Primitive Hematopoiesis

Inhibition of β-catenin signaling respecifies anterior-like endothelium into beating human cardiomyocytes

Associating transcription factors and conserved RNA structures with gene regulation in the human brain

6S RNA is a widespread regulator of eubacterial RNA polymerase that resembles an open promoter

Identification and characterization of novel conserved RNA structures in Drosophila

Glycolysis gene expression analysis and selective metabolic advantage in the clinical progression of colorectal cancer

Dihydropyrimidine dehydrogenase pharmacogenetics for predicting fluoropyrimidine-related toxicity in the randomised, phase III adjuvant TOSCA trial in high-risk colon cancer patients

Does rapid sequence divergence preclude RNA structure conservation in vertebrates?

widespread riboswitch candidate that controls bacterial genes involved in molybdenum cofactor and tungsten cofactor metabolism

Sexual ancestors generated an obligate asexual and globally dispersed clone within the model diatom species Thalassiosira pseudonana

Noncoding deletions reveal a gene that is critical for intestinal function

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