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Human Calmodulin Mutations

Frontiers in molecular neuroscience, 2018-11, Vol.11, p.396-396

2018

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Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

BMC genomics, 2015-07, Vol.16 (1), p.548-548, Article 548

2015

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Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

American journal of human genetics, 2012-10, Vol.91 (4), p.703-712

2012

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Gut microbiota profiles of autism spectrum disorder and attention deficit/hyperactivity disorder: A systematic literature review

Gut microbes, 2020-09, Vol.11 (5), p.1172-1187

2020

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Calmodulin mutations affecting Gly114 impair binding to the NaV1.5 IQ-domain

Frontiers in pharmacology, 2023-08, Vol.14, p.1210140

2023

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Therapeutic endometrial scratching and implantation after in vitro fertilization: a multicenter randomized controlled trial

Fertility and sterility, 2019-12, Vol.112 (6), p.1015-1021

2019

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Triploidy--Observations in 154 Diandric Cases

PloS one, 2015-11, Vol.10 (11), p.e0142545-e0142545

2015

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Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity

Genes, 2020-02, Vol.11 (3), p.268

2020

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Coronary artery disease-associated genetic variants and biomarkers of inflammation

PloS one, 2017-07, Vol.12 (7), p.e0180365

2017

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Children and adolescents with attention deficit hyperactivity disorder and autism spectrum disorder share distinct microbiota compositions

Gut microbes, 2023-12, Vol.15 (1), p.2211923-2211923

2023

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Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

Frontiers in aging neuroscience, 2017-12, Vol.9, p.413-413

2017

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CtIP Mutations Cause Seckel and Jawad Syndromes

PLoS genetics, 2011-10, Vol.7 (10), p.e1002310-e1002310

2011

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Infanticide vs. inherited cardiac arrhythmias

Europace (London, England), 2021-03, Vol.23 (3), p.441-450

2021

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PTPRG is an ischemia risk locus essential for HCO3–-dependent regulation of endothelial function and tissue perfusion

eLife, 2020-09, Vol.9

2020

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HSPA12A targets the cytoplasmic domain and affects the trafficking of the Amyloid Precursor Protein receptor SorLA

Scientific reports, 2019-01, Vol.9 (1), p.611-611, Article 611

2019

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Idiopathic early ovarian aging: is there a relation with premenopausal accelerated biological aging in young women with diminished response to ART?

Journal of assisted reproduction and genetics, 2021-11, Vol.38 (11), p.3027-3038

2021

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Multi-Trait Genomic Risk Stratification for Type 2 Diabetes

Frontiers in medicine, 2021-09, Vol.8, p.711208

2021

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Predicting the presence of coronary plaques featuring high-risk characteristics using polygenic risk scores and targeted proteomics in patients with suspected coronary artery disease

Genome medicine, 2024-03, Vol.16 (1), p.40-10, Article 40

2024

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Migraine-Associated Mutation in the Na,K-ATPase Leads to Disturbances in Cardiac Metabolism and Reduced Cardiac Function

Journal of the American Heart Association, 2022-04, Vol.11 (7), p.e021814-e021814

2022

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The insulin-like growth factor system in multiple myeloma: diagnostic and therapeutic potential

Oncotarget, 2016-07, Vol.7 (30), p.48732-48752

2016

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Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden

Journal of the American Heart Association, 2020-02, Vol.9 (3), p.e014795-e014795

2020

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Functionally Validating Evolutionary Conserved Risk Genes for Parkinson's Disease in Drosophila melanogaster

Insects (Basel, Switzerland), 2023-02, Vol.14 (2), p.168

2023

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Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

Human Calmodulin Mutations

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

Gut microbiota profiles of autism spectrum disorder and attention deficit/hyperactivity disorder: A systematic literature review

Calmodulin mutations affecting Gly114 impair binding to the NaV1.5 IQ-domain

Therapeutic endometrial scratching and implantation after in vitro fertilization: a multicenter randomized controlled trial

Triploidy--Observations in 154 Diandric Cases

Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity

Coronary artery disease-associated genetic variants and biomarkers of inflammation

Children and adolescents with attention deficit hyperactivity disorder and autism spectrum disorder share distinct microbiota compositions

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

DBDS Genomic Cohort, a prospective and comprehensive resource for integrative and temporal analysis of genetic, environmental and lifestyle factors affecting health of blood donors

CtIP Mutations Cause Seckel and Jawad Syndromes

Infanticide vs. inherited cardiac arrhythmias

PTPRG is an ischemia risk locus essential for HCO3–-dependent regulation of endothelial function and tissue perfusion

HSPA12A targets the cytoplasmic domain and affects the trafficking of the Amyloid Precursor Protein receptor SorLA

Idiopathic early ovarian aging: is there a relation with premenopausal accelerated biological aging in young women with diminished response to ART?

Multi-Trait Genomic Risk Stratification for Type 2 Diabetes

Danish study of Non-Invasive testing in Coronary Artery Disease 2 (Dan-NICAD 2): Study design for a controlled study of diagnostic accuracy

Predicting the presence of coronary plaques featuring high-risk characteristics using polygenic risk scores and targeted proteomics in patients with suspected coronary artery disease

Migraine-Associated Mutation in the Na,K-ATPase Leads to Disturbances in Cardiac Metabolism and Reduced Cardiac Function

The insulin-like growth factor system in multiple myeloma: diagnostic and therapeutic potential

Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden

Functionally Validating Evolutionary Conserved Risk Genes for Parkinson's Disease in Drosophila melanogaster

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