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Limitations of mitochondrial gene barcoding in Octocorallia

Molecular ecology resources, 2011-01, Vol.11 (1), p.19-31

2011

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Deep-sea octocorals and antipatharians show no evidence of seamount-scale endemism in the NW Atlantic

Marine ecology. Progress series (Halstenbek), 2009-12, Vol.397, p.25-35

2009

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Characterization of the zooxanthellate and azooxanthellate morphotypes of the Mediterranean gorgonian Eunicella singularis

Marine biology, 2012-07, Vol.159 (7), p.1485-1496

2012

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Molecular and Morphological Diversity of Sea Fans with Emphasis on Deep-sea Octocorals of the Order Alcyonacea Lamouroux, 1812

Thoma, Jana N

2013

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First-Line Nivolumab in Stage IV or Recurrent Non–Small-Cell Lung Cancer

The New England journal of medicine, 2017-06, Vol.376 (25), p.2415-2426

2017

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Nature genetics, 2011-10, Vol.43 (10), p.977-983

2011

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Nature genetics, 2020-05, Vol.52 (5), p.473-481

2020

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

Molecular psychiatry, 2020-07, Vol.25 (7), p.1430-1446

2020

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Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: a population-level modelling analysis

The Lancet infectious diseases, 2019-01, Vol.19 (1), p.56-66

2019

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Identification of common genetic risk variants for autism spectrum disorder

Nature genetics, 2019-03, Vol.51 (3), p.431-444

2019

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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature communications, 2019-06, Vol.10 (1), p.2548-18, Article 2548

2019

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Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

American journal of human genetics, 2015-02, Vol.96 (2), p.283-294

2015

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Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

American journal of human genetics, 2016-11, Vol.99 (5), p.1005-1014

2016

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Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

Molecular psychiatry, 2021-06, Vol.26 (6), p.2457-2470

2021

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Identification of pathways for bipolar disorder: a meta-analysis

JAMA psychiatry (Chicago, Ill.), 2014-06, Vol.71 (6), p.657

2014

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Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

Biological psychiatry (1969), 2018-07, Vol.84 (2), p.138-147

2018

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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

Nature communications, 2019-07, Vol.10 (1), p.3094-16, Article 3094

2019

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A 2-Year Randomized Controlled Trial of Human Caloric Restriction: Feasibility and Effects on Predictors of Health Span and Longevity

The journals of gerontology. Series A, Biological sciences and medical sciences, 2015-09, Vol.70 (9), p.1097-1104

2015

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All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

PLoS genetics, 2013-04, Vol.9 (4), p.e1003449-e1003449

2013

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2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

Arthritis & rheumatology (Hoboken, N.J.), 2016-03, Vol.68 (3), p.566-576

2016

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Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

American journal of human genetics, 2011-03, Vol.88 (3), p.372-381

2011

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Nirsevimab for Prevention of Hospitalizations Due to RSV in Infants

The New England journal of medicine, 2023-12, Vol.389 (26), p.2425-2435

2023

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Nature genetics, 2015-12, Vol.47 (12), p.1415-1425

2015

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TIM3+ TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C

The Journal of experimental medicine, 2022-02, Vol.219 (2)

2022

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Limitations of mitochondrial gene barcoding in Octocorallia

Deep-sea octocorals and antipatharians show no evidence of seamount-scale endemism in the NW Atlantic

Characterization of the zooxanthellate and azooxanthellate morphotypes of the Mediterranean gorgonian Eunicella singularis

Molecular and Morphological Diversity of Sea Fans with Emphasis on Deep-sea Octocorals of the Order Alcyonacea Lamouroux, 1812

Proteogenomics connects somatic mutations to signalling in breast cancer

First-Line Nivolumab in Stage IV or Recurrent Non–Small-Cell Lung Cancer

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: a population-level modelling analysis

Identification of common genetic risk variants for autism spectrum disorder

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

Identification of pathways for bipolar disorder: a meta-analysis

Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

A 2-Year Randomized Controlled Trial of Human Caloric Restriction: Feasibility and Effects on Predictors of Health Span and Longevity

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

Nirsevimab for Prevention of Hospitalizations Due to RSV in Infants

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

TIM3+ TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C

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