Author details

Full Name

Dale R Nyholt

Affiliation

ORCID

Career Start Year

1995

Papers

245

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
38087366	Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients: a longitudinal study.	Clin Epigenetics	2023
36819664	The shared genetic landscape of blood cell traits and risk of neurological and psychiatric disorders.		2023
36759319	Migraine genetics: Status and road forward.	Cephalalgia	2023
36808568	Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin.		2023
36807966	Migraine and thyroid dysfunction: Co-occurrence, shared genes and biological mechanisms.		2023
37245199	Integrating eQTL and GWAS data characterises established and identifies novel migraine risk loci.		2023
36739509	Shared genetics and causal relationships between migraine and thyroid function traits.		2023
36672757	Cross-Trait Genetic Analyses Indicate Pleiotropy and Complex Causal Relationships between Headache and Thyroid Function Traits.		2022
35710732	Integrative multi-omic analysis identifies genetically influenced DNA methylation biomarkers for breast and prostate cancers.	Communications Biology	2022
36292730	Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes.	Genes	2022
35627115	Glucose-Related Traits and Risk of Migraine-A Potential Mechanism and Treatment Consideration.	Genes	2022
35735024	Elucidating the relationship between migraine risk and brain structure using genetic data.	Brain	2022
35472084	Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.	Human Reproduction	2022
36400032	Shared genetic influences between blood analyte levels and risk of severe COVID-19.	Cell Reports	2022
35851147	A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders.	Communications Biology	2022
36699451	Genome-wide imputed differential expression enrichment analysis identifies trait-relevant tissues.		2022
34644541	Genetic overlap and causality between blood metabolites and migraine.	American Journal of Human Genetics	2021
34130515	Association and genetic overlap between clinical chemistry tests and migraine.	Cephalalgia	2021
34239411	Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine.	Frontiers in Neuroscience	2021
34064523	Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk.	Genes	2021
33989694	Genetic correlation analysis does not associate male pattern baldness with COVID-19.	Journal of the American Academy of Dermatology	2021
34089721	Polygenic Risk Scores Stratify Keratinocyte Cancer Risk among Solid Organ Transplant Recipients with Chronic Immunosuppression in a High Ultraviolet Radiation Environment.		2021
34088753	Polyunsaturated Fatty Acid Levels and the Risk of Keratinocyte Cancer: A Mendelian Randomization Analysis.	Cancer Epidemiology Biomarkers and Prevention	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
32959083	Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.	Hum Genet	2021
32615124	Polygenic Risk Scores Allow Risk Stratification for Keratinocyte Cancer in Organ-Transplant Recipients.		2021
34379077	Polygenic Risk Scores Derived From Varying Definitions of Depression and Risk of Depression.	JAMA Psychiatry	2021
33005726	Exploring the genetic relationship between hearing impairment and Alzheimer's disease.	Alzheimers Dement (Amst)	2020
32423498	Migraine, Human Genetics and a Passion for Science.	Twin Research and Human Genetics	2020
32121467	Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.	Genes (Basel)	2020
32056457	Mitochondrial genome-wide association study of migraine - the HUNT Study.	Cephalalgia	2020
31774481	A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping.	Briefings in Bioinformatics	2020
32341527	Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.	Nat Genet	2020
33239672	The genetic architecture of sporadic and multiple consecutive miscarriage.	Nat Commun	2020
33058326	Recognition and clinical implications of high prevalence of migraine in patients with Brugada syndrome and drug-induced type 1 Brugada pattern.	Journal of Cardiovascular Electrophysiology	2020
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
29911421	Linking migraine frequency with family history of migraine.	Cephalalgia	2019
30634909	Novel hypotheses emerging from GWAS in migraine?	J Headache Pain	2019
31268507	Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.	JAMA Psychiatry	2019
28058943	Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways.	Cephalalgia	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
29865051	Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels.	J Alzheimers Dis	2018
29995844	Molecular genetic overlap between migraine and major depressive disorder.	Eur J Hum Genet	2018
29357833	Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine.	BMC Genomics	2018
29700475	Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.	Nat Genet	2018
29608257	Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.	Cancer Med	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018