Genetics 59 Projects
01:25

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

Natasha H. J. Ng

0 views • 1 year ago

01:53

Advances in computer-assisted syndrome recognition and differentiation in a set of metabolic disorders

Jean Tori Pantel

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00:12

Characterization of Glycosylphosphatidylinositol Biosynthesis Defects by Clinical Features, Flow Cytometry, and Automated Image Analysis

Alexej Knaus

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02:02

Standardized biogeographic grouping system for annotating populations in pharmacogenetic research

Rachel Huddart

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01:37

Sex-specific genetic effects across biomarkers

Emily Flynn

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01:28

Drug Response Pharmacogenetics for 200,000 UK Biobank Participants

Greg McInnes

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02:27

LPA and APOE are associated with statin selection in the UK Biobank

Adam Lavertu

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01:28

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Christian R. Marshall

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01:21

Common risk variants identified in autism spectrum disorder

Jakob Grove

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01:14

Junction-skipping regulation in complex disease

Ruize Liu

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01:41

Population-specific causal disease effect sizes in functionally important regions impacted by selection

Huwenbo Shi

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01:33

Comparative genetic architectures of schizophrenia in East Asian and European populations

Max Lam

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01:33

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Padhraig Gormley

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02:15

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Manuel A Rivas

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01:31

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

Ditte Demontis

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01:32

Association mapping of inflammatory bowel disease loci to single variant resolution

Hailiang Huang

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01:14

Integrative genetic and epigenetic analysis uncovers regulatory mechanisms of autoimmune disease

Parisa Shooshtari

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02:11

RICOPILI: Rapid Imputation for COnsortias PIpeLIne

Max Lam

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02:32

Genome-wide maps of enhancer regulation connect risk variants to disease genes

Joseph Nasser

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02:10

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

Epi25 Collaborative

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01:22

Polygenic Prediction via Bayesian Regression and Continuous Shrinkage Priors

Tian Ge

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01:03

Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

Aysu Okbay

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01:35

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

Jason Flannick

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01:47

Polygenic Prediction of Type 2 Diabetes in Continental Africa

Tinashe Chikowore

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01:25

Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation

Oleksandr Frei

0 views • 1 year ago

02:55

Personalized genetic assessment of age associated Alzheimers disease risk

Rahul S. Desikan

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01:33

The genetic architecture of the human cerebral cortex

Katrina L. Grasby

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01:43

The genetic organization of subcortical volumetric change is stable throughout the lifespan

Anders M. Fjell

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01:46

Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

Iris E Jansen

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02:14

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Naomi R. Wray

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01:14

deMeta: Removing sub-studies from meta-analysis of genome wide association studies (GWAS)

Jiangming Sun

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01:16

Genomewide association study identifies 30 loci associated with bipolar disorder

Eli A. Stahl

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02:04

CXCR4 involvement in neurodegenerative diseases

Luke W. Bonham

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01:48

Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

Caroline M. Nievergelt

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02:21

A genetic risk score to guide age-specific, personalized prostate cancer screening

Tyler M Seibert

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02:42

Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics

Dominic Holland

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01:41

Stable heteroplasmy at the single cell level is facilitated by inter-cellular exchange of mtDNA

Anitha D Jayaprakash

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01:38

b3galt6 knock-out zebrafish recapitulate β3GalT6-deficiency disorders in human and reveal a trisaccharide proteoglycan linkage region

Sarah Delbaere

0 views • 1 year ago

01:53

A gene based approach to test genetic association based on an Optimally Weighted Combination of Multiple Traits

Jianjun Zhang

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01:40

Test Gene-Environment Interactions for Multiple Traits in Sequencing Association Studies

Jianjun Zhang

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01:40

Powerful statistical method to detect disease associated genes using publicly available GWAS summary data

Jianjun Zhang

0 views • 1 year ago

01:34

An Optimally Weighted Combination Method to Detect Novel Disease Associated Genes Using Publicly Available GWAS Summary Data

Jianjun Zhang

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01:39

Investigation Gene body methylation is under selection in Arabidopsis thaliana

Aline Muyle

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01:27

A missense variant in CREBRF is associated with taller stature in Samoans

Jenna C. Carlson

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01:10

Population sequencing data reveal a compendium of mutational processes in human germline

Vladimir B. Seplyarskiy

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02:48

Biological Pathways and Gene Networks Link Inflammation and Vascular Remodeling to Both Heart Failure with Preserved and Reduced Ejection Fraction in Women across Ethnicities

Qing Liu

0 views • 1 year ago

01:48

Discordant association of the CREBRF rs373863828 minor allele with increased body mass index and protection from type 2 diabetes in Māori and Pacific (Polynesian) people living in Aotearoa New Zealand

Mohanraj Krishnan

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01:40

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

Adrienne M Stilp

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01:37

Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels

Jenna C. Carlson

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01:58

Recovery of trait heritability from whole genome sequence data

Pierrick Wainschtein

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01:55

Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

George Hindy

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01:18

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox

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00:56

Mutations in EBF3 disturb transcriptional profiles and underlie a novel syndrome of intellectual disability, ataxia and facial dysmorphism

Frederike Leonie Harms

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01:27

Genome-wide methylation data mirror ancestry information

Elior Rahmani

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02:02

Whole Genome Sequencing of Pharmacogenetic Drug Response in Racially and Ethnically Diverse Children with Asthma

Angel Mak

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01:02

Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled

Sam Oh

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01:23

Existence and implications of population variance structure

Shaila Musharoff

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01:59

Variation in predicted COVID-19 risk among lemurs and lorises

Amanda D Melin

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00:29

Comparative ACE2 variation and primate COVID-19 risk

Amanda D Melin

0 views • 1 year ago