Nature Search

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

The autism spectrum disorders are complex genetic traits characterized by various neurodevelopmental deficits. Here, the authors analyse defective gene family interaction networks in autism cases and healthy controls and identify potential gene family interactions that may contribute to autism aetiology.

Dexter Hadley
Zhi-liang Wu
Hakon Hakonarson
ResearchOpen Access13 Jun 2014
Nature Communications

Volume: 5, P: 1-10
Global warming-induced upper-ocean freshening and the intensification of super typhoons

Super typhoons pose significant societal threats, yet their future behaviour due to rainfall-driven stratification changes remains unexplored. Here, observations and climate models reveal increased precipitation and subsequent freshening will likely intensify future super typhoons in the western N. Pacific.

Karthik Balaguru
Gregory R. Foltz
Kerry A. Emanuel
ResearchOpen Access25 Nov 2016
Nature Communications

Volume: 7, P: 1-8
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

Patrick Sleiman
Dai Wang
Qingqin Li
ResearchOpen Access29 Oct 2013
Scientific Reports

Volume: 3, P: 1-5
Precision annotation of digital samples in NCBI’s gene expression omnibus

Dexter Hadley
James Pan
Atul J. Butte
ResearchOpen Access19 Sept 2017
Scientific Data

Volume: 4, P: 1-11
Marine heatwaves as hot spots of climate change and impacts on biodiversity and ecosystem services

Marine heatwaves (MHWs) have become more intense and widespread globally, affecting species, ecosystems and people. After summarizing how and why MHWs are changing, this Review explores these impacts and their underlying mechanisms, highlights knowledge gaps and considers opportunities to mitigate the effects of MHWs.

Thomas Wernberg
Mads S. Thomsen
Katie Smith
Reviews07 Jul 2025
Nature Reviews Biodiversity

Volume: 1, P: 461-479
Prediction of future healthcare expenses of patients from chest radiographs using deep learning: a pilot study

Jae Ho Sohn
Yixin Chen
Youngho Seo
ResearchOpen Access18 May 2022
Scientific Reports

Volume: 12, P: 1-9
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Associations of copy number variations (CNVs) with complex traits are challenging to study because of their low frequency. Here, the authors analyse SNP array and array comparative genomic hybridization data of 100,028 individuals and report their associations with immune-related, cardiometabolic and neuropsychiatric diseases as well as cancer.

Yun Rose Li
Joseph T. Glessner
Hakon Hakonarson
ResearchOpen Access14 Jan 2020
Nature Communications

Volume: 11, P: 1-9
Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

H Rob Taal
Beate St Pourcain
James F Wilson
Amendments and Corrections29 May 2013
Nature Genetics

Volume: 45, P: 713
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume

M Arfan Ikram
Myriam Fornage
James F Wilson
Amendments and Corrections29 May 2013
Nature Genetics

Volume: 45, P: 713
Common variants at 12q15 and 12q24 are associated with infant head circumference

Vincent Jaddoe and colleagues report a genome-wide association study for infant head circumference. They identify variants in SBNO1 and near HMGA2 that are associated with this phenotype.

H Rob Taal
Beate St Pourcain
James F Wilson
Research15 Apr 2012
Nature Genetics

Volume: 44, P: 532-538
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Hakon Hakonarson and colleagues report a genome-wide copy number variation study in 3,506 cases of attention-deficit hyperactivity disorder. The authors identify a statistically significant enrichment of CNVs impacting metabotropic glutamate receptor genes.

Josephine Elia
Joseph T Glessner
Hakon Hakonarson
Research04 Dec 2011
Nature Genetics

Volume: 44, P: 78-84
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth

Nadav Rappoport
Jonathan Toung
Marina Sirota
ResearchOpen Access09 Jan 2018
Scientific Reports

Volume: 8, P: 1-11
Tracing diagnosis trajectories over millions of patients reveal an unexpected risk in schizophrenia

Hyojung Paik
Matthew J. Kan
Atul J. Butte
ResearchOpen Access15 Oct 2019
Scientific Data

Volume: 6, P: 1-10
Common variants at 6q22 and 17q21 are associated with intracranial volume

M. Arfan Ikram and colleagues report a genome-wide association study for intracranial volume and brain volume. They report two loci associated with intracranial volume.

M Arfan Ikram
Myriam Fornage
James F Wilson
Research15 Apr 2012
Nature Genetics

Volume: 44, P: 539-544
A merged microarray meta-dataset for transcriptionally profiling colorectal neoplasm formation and progression

Michael Rohr
Jordan Beardsley
Deborah Altomare
ResearchOpen Access11 Aug 2021
Scientific Data

Volume: 8, P: 1-11

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