Publication & Citation Trends
Publications
0 total
Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis
Cited by 0
Semantic Scholar
Genetic architecture of lumbar spinal stenosis
Cited by 0
Semantic Scholar
214 Longitudinal and Exploratory Genome-Wide Analysis in Alopecia AreaTA (LEGAATA): A Study of FinnGen Participants
Cited by 0
Semantic Scholar
Narcolepsy as a potential risk factor for Schizophrenia OA
Cited by 3
Semantic Scholar
Very-early-onset autoimmune hypothyroidism: a report of two cases with STAT3 gain-of-function variant
Cited by 0
Semantic Scholar
Phenome-wide association study of male and female sex chromosome trisomies in 1.5 million participants of MVP, FinnGen, and UK Biobank.
Cited by 2
Semantic Scholar
Research Topics
Genetic Associations and Epidemiology
(16)
Bioinformatics and Genomic Networks
(7)
BRCA gene mutations in cancer
(4)
Data Visualization and Analytics
(4)
Diabetes and associated disorders
(4)
Affiliations
Broad Institute
Brigham and Women's Hospital
National Institutes of Health
Children's Hospital of Philadelphia
University of Helsinki