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
Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.
Npj Systems Biology And Applications
Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A
Publication Date: 2021-01-08
Variant appearance in text: PLG: 2286T>G; G762G; rs11060
Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.
Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.
Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
G3 (Bethesda, Md.)
Sadovnick, A Dessa AD; Traboulsee, Anthony L AL; Bernales, Cecily Q CQ; Ross, Jay P JP; Forwell, Amanda L AL; Yee, Irene M IM; Guillot-Noel, Lena L; Fontaine, Bertrand B; Cournu-Rebeix, Isabelle I; Alcina, Antonio A; Fedetz, Maria M; Izquierdo, Guillermo G; Matesanz, Fuencisla F; Hilven, Kelly K; Dubois, Bénédicte B; Goris, An A; Astobiza, Ianire I; Alloza, Iraide I; Antigüedad, Alfredo A; Vandenbroeck, Koen K; Akkad, Denis A DA; Aktas, Orhan O; Blaschke, Paul P; Buttmann, Mathias M; Chan, Andrew A; Epplen, Joerg T JT; Gerdes, Lisa-Ann LA; Kroner, Antje A; Kubisch, Christian C; Kümpfel, Tania T; Lohse, Peter P; Rieckmann, Peter P; Zettl, Uwe K UK; Zipp, Frauke F; Bertram, Lars L; Lill, Christina M CM; Fernandez, Oscar O; Urbaneja, Patricia P; Leyva, Laura L; Alvarez-Cermeño, Jose Carlos JC; Arroyo, Rafael R; Garagorri, Aroa M AM; García-Martínez, Angel A; Villar, Luisa M LM; Urcelay, Elena E; Malhotra, Sunny S; Montalban, Xavier X; Comabella, Manuel M; Berger, Thomas T; Fazekas, Franz F; Reindl, Markus M; Schmied, Mascha C MC; Zimprich, Alexander A; Vilariño-Güell, Carles C
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