The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders (Q59737903)

From Wikidata

Jump to navigation Jump to search

article by A Jeremy Willsey et al published 26 July 2018 in Cell

Language	Label	Description	Also known as
English	The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders	article by A Jeremy Willsey et al published 26 July 2018 in Cell

Statements

scholarly article

0 references

The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders (English)

0 references

25

object named as

Nenad Sestan

0 references

object named as

Michael E Ward

26

0 references

Michael J Keiser

object named as

Michael J Keiser

19

0 references

object named as

Loren M Frank

30

0 references

object named as

Hugo J Bellen

29

0 references

Mark von Zastrow

21

object named as

Mark von Zastrow

0 references

Jennifer Doudna

13

object named as

Jennifer Doudna

0 references

34

object named as

Trey Ideker

0 references

Tomasz Nowakowski

28

object named as

Tomasz J Nowakowski

0 references

36

object named as

Nevan J Krogan

0 references

Daniel H. Lowenstein

16

object named as

Daniel H Lowenstein

0 references

22

object named as

Lennart Mucke

0 references

10

object named as

Tejal A Desai

0 references

author name string

A Jeremy Willsey

1

0 references

Montana T Morris

2

0 references

Sheng Wang

3

0 references

Helen R Willsey

4

0 references

Nawei Sun

5

0 references

Nia Teerikorpi

6

0 references

Tierney B Baum

7

0 references

Gerard Cagney

8

0 references

Kevin J Bender

9

0 references

Deepak Srivastava

11

0 references

Graeme W Davis

12

0 references

Edward Chang

14

0 references

Vikaas Sohal

15

0 references

Hao Li

17

0 references

David Agard

18

0 references

Brian Shoichet

20

0 references

Steven Finkbeiner

23

0 references

Li Gan

24

0 references

Ruth Huttenhain

27

0 references

Mustafa K Khokha

31

0 references

Richard P Lifton

32

0 references

Martin Kampmann

33

0 references

Matthew W State

35

0 references

language of work or name

0 references

publication date

26 July 2018

0 references

0 references

174

0 references

3

0 references

505-520

0 references

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activins are expressed early in Xenopus embryogenesis and can induce axial mesoderm and anterior structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neural induction by the secreted polypeptide noggin

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line transmission of transgenes in Xenopus laevis

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene ontology: tool for the unification of biology

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms of human hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xenopus tropicalis transgenic lines and their use in the study of embryonic induction

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A census of human cancer genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Similar network activity from disparate circuit parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global landscape of protein complexes in the yeast Saccharomyces cerevisiae

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homeostatic control of neural activity: from phenomenology to molecular design

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of clustering algorithms for protein-protein interaction networks

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple vertebrate models for chemical genetics and drug discovery screens: lessons from zebrafish and Xenopus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile x mental retardation protein regulates proliferation and differentiation of adult neural stem/progenitor cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genome of the Western clawed frog Xenopus tropicalis

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative genetic interactions reveal biological modularity

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Boosting signal-to-noise in complex biology: prior knowledge is power

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Challenges in neurodegeneration research

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Self-organizing optic-cup morphogenesis in three-dimensional culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seizure and epilepsy: studies of seizure disorders in Drosophila

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discovery of mutated subnetworks associated with clinical data in cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global landscape of HIV-human protein complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of drug combinations by integrating molecular and pharmacological data

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insights into cortical oscillations arising from optogenetic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aversive training methods in Xenopus laevis: general principles

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroscience. The emerging biology of autism spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic exome sequencing in persons with severe intellectual disability

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene ontology inferred from molecular networks

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting functional effect of human missense mutations using PolyPhen-2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A systematic mammalian genetic interaction map reveals pathways underlying ricin susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative genetic-interaction mapping in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An updated overview of animal models in neuropsychiatry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo mutations in histone-modifying genes in congenital heart disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Integrated platform for genome-wide screening and construction of high-density genetic interaction maps in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The state of US health, 1990-2010: burden of diseases, injuries, and risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developing zebrafish models of autism spectrum disorder (ASD).

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo mutations in schizophrenia implicate synaptic networks

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The developmental transcriptome of the human brain: implications for neurodevelopmental disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric disorders: diagnosis to therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biological insights from 108 schizophrenia-associated genetic loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

STRING v10: protein-protein interaction networks, integrated over the tree of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo mutations in moderate or severe intellectual disability

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synaptic, transcriptional and chromatin genes disrupted in autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism spectrum disorders: from genes to neurobiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global mapping of herpesvirus-host protein complexes reveals a transcription strategy for late genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gamma rhythms link prefrontal interneuron dysfunction with cognitive inflexibility in Dlx5/6(+/-) mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FMRP regulates neurogenesis in vivo in Xenopus laevis tadpoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysfunctional prefrontal gamma-band oscillations reflect working memory and other cognitive deficits in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards large-scale, human-based, mesoscopic neurotechnologies

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell-based screening: extracting meaning from complex data

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene hunting in autism spectrum disorder: on the path to precision medicine

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cancer cell map initiative: defining the hallmark networks of cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Putative Microcircuit-Level Substrates for Attention Are Disrupted in Mouse Models of Autism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global Mapping of the Inc-Human Interactome Reveals that Retromer Restricts Chlamydia Infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The BioPlex Network: A Systematic Exploration of the Human Interactome

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative mapping of host-pathogen protein-protein interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Associations Between Maternal Infection During Pregnancy, Childhood Infections, and the Risk of Subsequent Psychotic Disorder--A Swedish Cohort Study of Nearly 2 Million Individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translation of Genotype to Phenotype by a Hierarchy of Cell Subsystems

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Color and intensity discrimination in Xenopus laevis tadpoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal Infection during Pregnancy and Risk of Autism Spectrum Disorders: A Systematic Review and Meta-analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HPIDB 2.0: a curated database for host-pathogen interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A scored human protein-protein interaction network to catalyze genomic interpretation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association Between Influenza Infection and Vaccination During Pregnancy and Risk of Autism Spectrum Disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and architecture of de novo mutations in developmental disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal maternal immune activation and brain development with relevance to psychiatric disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combinatorial CRISPR-Cas9 screens for de novo mapping of genetic interactions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimating the selective effects of heterozygous protein-truncating variants from human exome data.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De Novo Coding Variants Are Strongly Associated with Tourette Disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic interaction mapping in mammalian cells using CRISPR interference

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A subcellular map of the human proteome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Whole cell maps chart a course for 21st-century cell biology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endo-lysosomal dysfunction: a converging mechanism in neurodegenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fully integrated silicon probes for high-density recording of neural activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic strategies to tackle neurological diseases in fruit flies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physiology Flies with Time.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dual gene activation and knockout screen reveals directional dependencies in genetic networks.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene-specific T2A-GAL4 library for Drosophila.

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/30053424

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.CELL.2018.06.016

0 references

0 references

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q59737903&oldid=2018470576"