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D. Nyholt · SciRah

Researcher profile · Semantic Scholar

D. Nyholt

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D. Nyholt — researcher profile on SciRah

h-index: 92
Works: 350
Citations: 56K

Most-cited papers

Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +217 more
2018Nature Genetics1,852 citations Open access
Semantic Scholar
Genetic insights into biological mechanisms governing human ovarian ageing
K. Ruth, F. Day, Jazib Hussain, Ana Martínez-Marchal +264 more
2021Nature341 citations Open access
Semantic Scholar
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, B. Winsvold, S. Ruotsalainen, G. Bjornsdottir +67 more
2021Nature Genetics337 citations Open access
Semantic Scholar
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
Y. Sapkota, V. Steinthorsdottir, A. Morris, A. Fassbender +39 more
2017Nature Communications319 citations Open access
Semantic Scholar
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
N. Rahmioglu, S. Mortlock, Marzieh Ghiasi, P. L. Møller +129 more
2023Nature Genetics245 citations Open access
Semantic Scholar
Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility
M. Landi, D. Bishop, S. Macgregor, M. Machiela +148 more
2020Nature Genetics198 citations Open access
Semantic Scholar
A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts
G. Ni, Jian Zeng, J. Revez, Ying Wang +10 more
2021Biological Psychiatry173 citations Open access
Semantic Scholar
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Chen Li, S. Stoma, L. Lotta, S. Warner +92 more
2020American Journal of Human Genetics155 citations Open access
Semantic Scholar
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
C. Gallagher, N. Mäkinen, H. Harris, N. Rahmioglu +32 more
2019Nature Communications136 citations Open access
Semantic Scholar
Associations of autozygosity with a broad range of human phenotypes
D. Clark, Y. Okada, K. Moore, D. Mason +432 more
2019Nature Communications115 citations Open access
Semantic Scholar
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
D. Duffy, Gu Zhu, Xin Li, Marianna Sanna +102 more
2017Nature Communications112 citations Open access
Semantic Scholar
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns
D. Czamara, G. Eraslan, C. Page, J. Lahti +225 more
2019Nature Communications109 citations Open access
Semantic Scholar
Genome-wide association study identifies 48 common genetic variants associated with handedness
Gabriel Cuellar Partida, J. Tung, N. Eriksson, E. Albrecht +114 more
2019bioRxiv101 citations Open access
Semantic Scholar
The genetic architecture of sporadic and multiple consecutive miscarriage
T. Laisk, A. Soares, T. Ferreira, J. Painter +51 more
2020Nature Communications98 citations Open access
Semantic Scholar
Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity
Emmanuel Olorunleke Adewuyi, Y. Sapkota, A. Auta, K. Yoshihara +5 more
2020Genes82 citations Open access
Semantic Scholar
Genetic overlap between endometriosis and endometrial cancer: evidence from cross‐disease genetic correlation and GWAS meta‐analyses
J. Painter, T. O'Mara, A. Morris, Timothy H. T. Cheng +72 more
2018Cancer Medicine81 citations Open access
Semantic Scholar
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
S. Heilmann-Heimbach, C. Herold, L. Hochfeld, A. M. Hillmer +32 more
2017Nature Communications79 citations Open access
Semantic Scholar
A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer’s disease and gastrointestinal tract disorders
Emmanuel Olorunleke Adewuyi, Eleanor K. O'Brien, D. Nyholt, T. Porter +1 more
2022Communications Biology77 citations Open access
Semantic Scholar
Genetic effects influencing risk for major depressive disorder in China and Europe
Tim Bigdeli, S. Ripke, R. Peterson, M. Trzaskowski +93 more
2017Translational Psychiatry75 citations Open access
Semantic Scholar
Molecular genetic overlap between migraine and major depressive disorder
Yuanhao Yang, Hui-Ying Zhao, D. Boomsma, L. Ligthart +107 more
2018European Journal of Human Genetics71 citations Open access
Semantic Scholar
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes
L. Rietschel, F. Streit, Gu Zhu, K. McAloney +231 more
2017Scientific Reports63 citations Open access
Semantic Scholar
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine
Yanjun Guo, P. Rist, I. Daghlas, F. Giulianini +129 more
2020Nature Communications61 citations Open access
Semantic Scholar
A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping
A. Sathyanarayanan, Rohit Gupta, E. Thompson, D. Nyholt +2 more
2019Briefings Bioinform.59 citations Open access
Semantic Scholar
Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.
Sathish Periyasamy, S. John, R. Padmavati, P. Rajendren +27 more
2019JAMA psychiatry57 citations Open access
Semantic Scholar
Polygenic Risk Scores Derived From Varying Definitions of Depression and Risk of Depression.
B. Mitchell, Jackson G. Thorp, Ye-Da Wu, A. Campos +9 more
2021JAMA psychiatry56 citations Open access
Semantic Scholar
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality
Emmanuel Olorunleke Adewuyi, D. Mehta, Y. Sapkota, A. Auta +8 more
2020Human Genetics56 citations Open access
Semantic Scholar
Genome-wide association study identifies 48 common genetic variants associated with handedness
G. Cuéllar-Partida, J. Tung, N. Eriksson, E. Albrecht +114 more
2020Nature Human Behaviour56 citations Open access
Semantic Scholar
Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine
Zachary F. Gerring, A. McRae, G. Montgomery, D. Nyholt
2018BMC Genomics51 citations Open access
Semantic Scholar
Linking migraine frequency with family history of migraine
N. Pelzer, M. Louter, E. V. van Zwet, D. Nyholt +4 more
2018Cephalalgia49 citations Open access
Semantic Scholar
A causal effects of gut microbiota in the development of migraine
Qiang He, Wenjing Wang, Yang Xiong, Chuan-Yuan Tao +69 more
2023The Journal of Headache and Pain47 citations Open access
Semantic Scholar
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache
Katherine M. Siewert, D. Klarin, S. Damrauer, Kyong-Mi Chang +130 more
2020International Journal of Epidemiology45 citations Open access
Semantic Scholar
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
K. Kentistou, L. R. Kaisinger, S. Stankovic, Marc Vaudel +217 more
2024Nature Genetics40 citations Open access
Semantic Scholar
Genetic overlap and causality between blood metabolites and migraine.
H. M. Tanha, A. Sathyanarayanan, D. Nyholt
2021American Journal of Human Genetics40 citations Open access
Semantic Scholar
Genome-wide analysis of blood gene expression in migraine implicates immune-inflammatory pathways
Zachary F. Gerring, J. Powell, G. Montgomery, D. Nyholt
2018Cephalalgia39 citations Open access
Semantic Scholar
Novel hypotheses emerging from GWAS in migraine?
A. M. van den Maagdenberg, D. Nyholt, V. Anttila
2019The Journal of Headache and Pain34 citations Open access
Semantic Scholar
Exploring the genetic relationship between hearing impairment and Alzheimer's disease
B. Mitchell, Jackson G. Thorp, D. Evans, D. Nyholt +2 more
2020Alzheimer's & Dementia33 citations Open access
Semantic Scholar
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression
K. Glanville, J. Coleman, K. Hanscombe, J. Euesden +202 more
2020Biological Psychiatry32 citations Open access
Semantic Scholar
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
Lei Zhao, Wenhui Zhao, V. Anttila, V. Artto +66 more
2023The Journal of Headache and Pain26 citations Open access
Semantic Scholar
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Valérie Turcot, Ying-Chang Lu, H. Highland, C. Schurmann +396 more
2018Nature Genetics25 citations Open access
Semantic Scholar
Glucose-Related Traits and Risk of Migraine—A Potential Mechanism and Treatment Consideration
Md. Rafiqul Islam, D. Nyholt
2022Genes24 citations Open access
Semantic Scholar
Migraine genetics: Status and road forward
A. V. Harder, G. Terwindt, D. Nyholt, A. M. van den Maagdenberg
2023Cephalalgia23 citations Open access
Semantic Scholar
Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus
P. Kho, S. Mortlock, P. Rogers, D. Nyholt +4 more
2021Human Genetics23 citations Open access
Semantic Scholar
Mitochondrial genome-wide association study of migraine – the HUNT Study
S. Børte, J. Zwart, A. Skogholt, M. Gabrielsen +14 more
2020Cephalalgia22 citations Open access
Semantic Scholar
Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine
Charlotte K. Bainomugisa, H. Sutherland, R. Parker, A. McRae +9 more
2021Frontiers in Neuroscience21 citations Open access
Semantic Scholar
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank
M. Barbu, Yan-Ni Zeng, Xue-Yi Shen, S. Cox +228 more
2019Biological Psychiatry: Cognitive Neuroscience and Neuroimaging21 citations Open access
Semantic Scholar
Migraine and thyroid dysfunction: Co‐occurrence, shared genes and biological mechanisms
S. Tasnim, D. Nyholt
2023European Journal of Neurology20 citations Open access
Semantic Scholar
Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.
Emmanuel Olorunleke Adewuyi, D. Mehta, D. Nyholt
2022Human Reproduction20 citations Open access
Semantic Scholar
Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients: a longitudinal study
Divya Mehta, I. de Boer, H. Sutherland, J. Pijpers +7 more
2023Clinical Epigenetics19 citations Open access
Semantic Scholar
A comprehensive evaluation of polygenic score methods across cohorts in psychiatric disorders
Gui-Yan Ni, Jian Zeng, J. Revez, Ying Wang +9 more
2020medRxiv18 citations Open access
Semantic Scholar

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