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Paper Details

Thirty novel sequence variants impacting human intracranial volume.
Brain Commun
1
2022
Parkinson's disease, associating sequence variants, attention deficit hyperactivity disorder, confounder, cranial synostosis, human, intracranial volume associated variants, microcephaly, neurological disorders, neuroticism, sequence variants, transcript
Author NameAffiliation
Graham R WaltersdeCODE genetics/Amgen Inc.
Graham R WaltersUniversity of Iceland
Gyda BjornsdottirdeCODE genetics/Amgen Inc.
Egil FerkingstaddeCODE genetics/Amgen Inc.
Gudmar ThorleifssondeCODE genetics/Amgen Inc.
Gudmar ThorleifssondeCODE genetics/Amgen Inc.
Hilma HolmdeCODE genetics/Amgen Inc.
Unnur ThorsteinsdottirdeCODE genetics/Amgen Inc.
Unnur ThorsteinsdottirdeCODE genetics/Amgen Inc.
Patrick SulemdeCODE genetics/Amgen Inc.
Daniel F GudbjartssondeCODE genetics/Amgen Inc.
Hreinn StefanssondeCODE genetics/Amgen Inc.
Thorgeir E ThorgeirssondeCODE genetics/Amgen Inc.
Magnus O UlfarssondeCODE genetics/Amgen Inc.
Magnus O UlfarssonUniversity of Iceland
Kari StefanssondeCODE genetics/Amgen Inc.
Kari StefanssonUniversity of Iceland
Kari StefanssondeCODE genetics/Amgen Inc.
Kari StefanssonUniversity of Iceland
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