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Number of items: 4.


Gormley, Padhraig, Kurki, Mitja I, Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A, Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli
et al (show 124 more authors) (2018) Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98 (4). 743 - 753.e4.


Bryois, Julien, Skene, Nathan G ORCID: 0000-0002-6807-3180, Hansen, Thomas Folkmann ORCID: 0000-0001-6703-7762, Kogelman, Lisette JA, Watson, Hunna J ORCID: 0000-0001-8405-381X, Liu, Zijing, Eating Disorders Working Group of the Psychiatric Genomics Conso, , International Headache Genetics Consortium, , 23andMe Research Team, , Brueggeman, Leo
et al (show 5 more authors) (2020) Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. Nature genetics, 52 (5). 482 - 493.


Forstner, Andreas J, Awasthi, Swapnil, Wolf, Christiane, Maron, Eduard, Erhardt, Angelika, Czamara, Darina, Eriksson, Elias, Lavebratt, Catharina, Allgulander, Christer, Friedrich, Nina
et al (show 65 more authors) (2021) Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. MOLECULAR PSYCHIATRY, 26 (8). 4179 - 4190.


Kogelman, Lisette JA, Esserlind, Ann-Louise, Christensen, Anne Francke, Awasthi, Swapnil, Ripke, Stephan, Ingason, Andres, Davidsson, Olafur B, Erikstrup, Christian, Hjalgrim, Henrik, Ullum, Henrik
et al (show 85 more authors) (2019) Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Neurology Genetics, 5 (6).

This list was generated on Wed Aug 3 02:32:44 2022 BST.