Author details

Full Name

Graham R Walters

Affiliation

ORCID

Career Start Year

2001

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37334623	Multi-polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives.	Am J Med Genet B Neuropsychiatr Genet	2024
37946686	Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD.	Am J Med Genet B Neuropsychiatr Genet	2024
37301908	Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37400429	Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37244984	DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.	BMC Genom Data	2023
33615640	Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.	Hum Brain Mapp	2022
36151456	Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample.	Mol Psychiatry	2022
36415660	Thirty novel sequence variants impacting human intracranial volume.	Brain Commun	2022
34620984	A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.	Commun Biol	2021
36070241	Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases.	BMJ Open	2021
33453761	Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.	Lancet Child Adolesc Health	2021
33931204	Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition.	Biol Psychiatry	2021
33602968	A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.	Sci Rep	2021
30705424	Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.	Mol Psychiatry	2020
32061372	Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment.	Biol Psychiatry	2020
31665216	Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.	JAMA Psychiatry	2020
30478444	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.	Nat Genet	2019
31624239	Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.	Transl Psychiatry	2019
30583851	Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.	Biol Psychiatry	2019
29364747	Rare and Common Variants Conferring Risk of Tooth Agenesis.	J Dent Res	2018
30150678	MAP1B mutations cause intellectual disability and extensive white matter deficit.	Nat Commun	2018
28223688	Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.	Nat Commun	2017
28596592	Sequence variant at 4q25 near PITX2 associates with appendicitis.	Sci Rep	2017
28440815	15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.	Transl Psychiatry	2017
28607503	Reproductive fitness and genetic risk of psychiatric disorders in the general population.	Nat Commun	2017
27848971	Epigenetic and genetic components of height regulation.	Nat Commun	2016
26053403	Polygenic risk scores for schizophrenia and bipolar disorder predict creativity.	Nat Neurosci	2015
25807286	Large-scale whole-genome sequencing of the Icelandic population.	Nat Genet	2015
24352232	CNVs conferring risk of autism or schizophrenia affect cognition in controls.	Nature	2014
23644456	Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.	Nature	2013
24084939	A common biological basis of obesity and nicotine addiction.	Transl Psychiatry	2013
24036950	A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.	Nat Genet	2013
22238593	A genome-wide association search for type 2 diabetes genes in African Americans.	PLoS One	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22914163	Rate of de novo mutations and the importance of father's age to disease risk.	Nature	2012
22267200	Discovery of common variants associated with low TSH levels and thyroid cancer risk.	Nat Genet	2012
21983786	Identification of low-frequency variants associated with gout and serum uric acid levels.	Nat Genet	2011
21427129	Common genetic variants associated with open-angle glaucoma.	Hum Mol Genet	2011
21378987	A rare variant in MYH6 is associated with high risk of sick sinus syndrome.	Nat Genet	2011
21357676	Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.	Hum Mol Genet	2011
20581827	Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.	Nat Genet	2010
20981099	Fine-scale recombination rate differences between sexes, populations and individuals.	Nature	2010
20835238	Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.	Nat Genet	2010
20935630	Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.	Nat Genet	2010
20935629	Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.	Nat Genet	2010
20622881	Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.	Nat Genet	2010
20081858	New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.	Nat Genet	2010
19557161	Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.	PLoS Genet	2009
19079262	New sequence variants associated with bone mineral density.	Nat Genet	2009
19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Nat Genet	2009