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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and SCP2[original query]
An approach based on a genome-wide association study reveals candidate loci for narcolepsy.
Human genetics 2010 Oct 128 (4): 433-41.
Shimada Mihoko, Miyagawa Taku, Kawashima Minae, Tanaka Susumu, Honda Yutaka, Honda Makoto, Tokunaga Katsus
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Clinical genetics 2021 3 100 (1): 59-78.
Mohseni Marzieh, Babanejad Mojgan, Booth Kevin T, Jamali Payman, Jalalvand Khadijeh, Davarnia Behzad, Ardalani Fariba, Khoshaeen Atefeh, Arzhangi Sanaz, Ghodratpour Fatemeh, Beheshtian Maryam, Jahanshad Faezeh, Otukesh Hasan, Bahrami Fatemeh, Seifati Seyed Morteza, Bazazzadegan Niloofar, Habibi Farkhonde, Behravan Hanieh, Mirzaei Sepide, Keshavarzi Fatemeh, Nikzat Nooshin, Mehrjoo Zohreh, Thiele Holger, Nothnagel Michael, Azaiez Hela, Smith Richard J, Kahrizi Kimia, Najmabadi Hosse
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases.
EBioMedicine 2022 2 77 103869.
Kolarova Hana, Tan Jing, Strom Tim M, Meitinger Thomas, Wagner Matias, Klopstock Thom
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