| Year |
Citation |
Score |
| 2024 |
Karadag N, Hagen E, Shadrin AA, van der Meer D, O'Connell KS, Rahman Z, Kutrolli G, Parker N, Bahrami S, Fominykh V, Heuser K, Taubøll E, Ueland T, Steen NE, Djurovic S, et al. Unraveling the shared genetics of common epilepsies and general cognitive ability. Medrxiv : the Preprint Server For Health Sciences. PMID 38585944 DOI: 10.1101/2024.03.25.24304773 |
0.432 |
|
| 2024 |
Shadrin AA, Hindley G, Hagen E, Parker N, Tesfaye M, Jaholkowski P, Rahman Z, Kutrolli G, Fominykh V, Djurovic S, Smeland OB, O'Connell KS, van der Meer D, Frei O, Andreassen OA, et al. Dissecting the genetic overlap between three complex phenotypes with trivariate MiXeR. Medrxiv : the Preprint Server For Health Sciences. PMID 38464132 DOI: 10.1101/2024.02.23.24303236 |
0.435 |
|
| 2023 |
Smeland OB, Kutrolli G, Bahrami S, Fominykh V, Parker N, Hindley GFL, Rødevand L, Jaholkowski P, Tesfaye M, Parekh P, Elvsåshagen T, Grotzinger AD, Steen NE, van der Meer D, O'Connell KS, et al. Genome-wide analyses reveal widespread genetic overlap between neurological and psychiatric disorders and a convergence of biological associations related to the brain. Medrxiv : the Preprint Server For Health Sciences. PMID 37503175 DOI: 10.1101/2023.07.21.23292993 |
0.507 |
|
| 2023 |
Jaholkowski P, Shadrin AA, Jangmo A, Frei E, Tesfaye M, Hindley GFL, Haram M, Rahman Z, Athanasiu L, Bakken NR, Holen B, Fominykh V, Kutrolli G, Parekh P, Parker N, et al. Associations Between Symptoms of Premenstrual Disorders and Polygenic Liability for Major Psychiatric Disorders. Jama Psychiatry. PMID 37163253 DOI: 10.1001/jamapsychiatry.2023.1137 |
0.377 |
|
| 2023 |
Karadag N, Shadrin AA, O'Connell K, Hindley GFL, Rahman Z, Parker N, Bahrami S, Fominykh V, Cheng W, Holen B, Alvestad S, Taubøll E, Steen NE, Djurovic S, Dale AM, et al. Identification of novel genomic risk loci shared between common epilepsies and psychiatric disorders. Brain : a Journal of Neurology. PMID 36757824 DOI: 10.1093/brain/awad038 |
0.432 |
|
| 2022 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Fominykh V, et al. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. PMID 35102318 DOI: 10.1038/s41588-022-01020-3 |
0.33 |
|
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