Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.
Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Whole-genome sequencing of the world's oldest people.
Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014
Variant appearance in text: COMT: N39N; rs74745580
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Biological Psychiatry
Gothelf, Doron D; Law, Amanda J AJ; Frisch, Amos A; Chen, Jingshan J; Zarchi, Omer O; Michaelovsky, Elena E; Ren-Patterson, Renee R; Lipska, Barbara K BK; Carmel, Miri M; Kolachana, Bhaskar B; Weizman, Abraham A; Weinberger, Daniel R DR