Eric

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Syddansk Universitet Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies Masnada,

Vinodh, J. Conroy, S. Sisodiya, 2017 .

Genetics Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG 2 as a Candidate Gene for Age-Related Macular Degeneration

Caroline, Craig, Ahn, 2019 .

The World Health Organization (WHO) classification recognizes a group of myeloid neoplasms with overlapping features of both myelodysplastic syndromes (MDS) and myeloproliferative neoplasms

A. Bagg, P. Fox, D. Arber, 2014 .

The Primary Open-Angle African-American Glaucoma Genetics (POAAGG) Study: Baseline Demographics

Emily S. Charlson, G. Ying, J. O'Brien, 2015 .

16 q 24 . 1 microdeletion in a premature newborn : usefulness of array-based comparative genomic hybridation ( array CGH ) in persistent pulmonary hypertension of the newborn

P. Stankiewicz, Z. Xia, J. Beckmann, 2013 .

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study

Elizabeth, Sandro, Ying-xue, 2018 .

A Specific Superoxide Dismutase Mutation Is on the Same Genetic Background in Sporadic and Familial Cases of Amyotrophic Lateral Sclerosis

B. Wirth, K. Zerres, T. Voit, 2007 .

Protective association of HLA‐DRB1*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences

Henrik, Michaël E. Belloy, Kaj, 2022, Alzheimer's & Dementia.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Hoffmann, Hartmann, Roussos, 2017, Scientific Reports.

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder

Li, Katharina, Warren W. Kretzschmar, 2018 .

Genome-Wide Association Study Implicates HLA-C * 01 : 02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia Irish Schizophrenia Genomics

Kelleher, P. Deloukas, E. Bramon, 2012 .

Peripheral nervous system alterations in disease and injury

Eric, E. Villalón, Villalón Landeros, 2016 .

Real-world genetic screening with molecular ancestry supports comprehensive pan-ethnic carrier screening

Schadt, L. Edelmann, B. Webb, 2022, medRxiv.

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies : The CHARGE Consortium Dehghan

Alanna, Res, O. Franco, 2016 .

risk variants and refine the genetic architecture ofmajor depressive disorder

Li, Katharina, Warren W. Kretzschmar, 2022 .