A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case report.
Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Wang, Tianyun T; Kim, Chang N CN; Bakken, Trygve E TE; Gillentine, Madelyn A MA; Henning, Barbara B; Mao, Yafei Y; Gilissen, Christian C; , ; Nowakowski, Tomasz J TJ; Eichler, Evan E EE
Publication Date: 2022-11-15
Variant appearance in text: BBS2: 1237C>T; Arg413*
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Nature Genetics
Zhou, Xueya X; Feliciano, Pamela P; Shu, Chang C; Wang, Tianyun T; Astrovskaya, Irina I; Hall, Jacob B JB; Obiajulu, Joseph U JU; Wright, Jessica R JR; Murali, Shwetha C SC; Xu, Simon Xuming SX; Brueggeman, Leo L; Thomas, Taylor R TR; Marchenko, Olena O; Fleisch, Christopher C; Barns, Sarah D SD; Snyder, LeeAnne Green LG; Han, Bing B; Chang, Timothy S TS; Turner, Tychele N TN; Harvey, William T WT; Nishida, Andrew A; O'Roak, Brian J BJ; Geschwind, Daniel H DH; , ; Michaelson, Jacob J JJ; Volfovsky, Natalia N; Eichler, Evan E EE; Shen, Yufeng Y; Chung, Wendy K WK
A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (BBS2) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog.
Genes
Hitti-Malin, Rebekkah J RJ; Burmeister, Louise M LM; Lingaas, Frode F; Kaukonen, Maria M; Pettinen, Inka I; Lohi, Hannes H; Sargan, David D; Mellersh, Cathryn S CS
Integrated molecular drivers coordinate biological and clinical states in melanoma.
Nature Genetics
Conway, Jake R JR; Dietlein, Felix F; Taylor-Weiner, Amaro A; AlDubayan, Saud S; Vokes, Natalie N; Keenan, Tanya T; Reardon, Brendan B; He, Meng Xiao MX; Margolis, Claire A CA; Weirather, Jason L JL; Haq, Rizwan R; Schilling, Bastian B; Stephen Hodi, F F; Schadendorf, Dirk D; Liu, David D; Van Allen, Eliezer M EM
Forty-five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor.
Nature Communications
Murphy, Andrew J AJ; Chen, Xiang X; Pinto, Emilia M EM; Williams, Justin S JS; Clay, Michael R MR; Pounds, Stanley B SB; Cao, Xueyuan X; Shi, Lei L; Lin, Tong T; Neale, Geoffrey G; Morton, Christopher L CL; Woolard, Mary A MA; Mulder, Heather L HL; Gil, Hyea Jin HJ; Rehg, Jerold E JE; Billups, Catherine A CA; Harlow, Matthew L ML; Dome, Jeffrey S JS; Houghton, Peter J PJ; Easton, John J; Zhang, Jinghui J; George, Rani E RE; Zambetti, Gerard P GP; Davidoff, Andrew M AM
Optimizing clinical exome design and parallel gene-testing for recessive genetic conditions in preconception carrier screening: Translational research genomic data from 14,125 exomes.
Plos Genetics
Capalbo, Antonio A; Valero, Roberto Alonso RA; Jimenez-Almazan, Jorge J; Pardo, Pere Mir PM; Fabiani, Marco M; Jiménez, David D; Simon, Carlos C; Rodriguez, Julio Martin JM
Publication Date: 2019-10
Variant appearance in text: BBS2: 1237C>T; Arg413*; rs147030232
Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.
Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies.
Scientific Reports
Sanchez-Navarro, Iker I; R J da Silva, Luciana L; Blanco-Kelly, Fiona F; Zurita, Olga O; Sanchez-Bolivar, Noelia N; Villaverde, Cristina C; Lopez-Molina, Maria Isabel MI; Garcia-Sandoval, Blanca B; Tahsin-Swafiri, Saoud S; Minguez, Pablo P; Riveiro-Alvarez, Rosa R; Lorda, Isabel I; Sanchez-Alcudia, Rocío R; Perez-Carro, Raquel R; Valverde, Diana D; Liu, Yichuan Y; Tian, Lifeng L; Hakonarson, Hakon H; Avila-Fernandez, Almudena A; Corton, Marta M; Ayuso, Carmen C
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Scientific Reports
Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE
Publication Date: 2017-04-25
Variant appearance in text: BBS2: R413X; rs147030232
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum.
Scientific Reports
Maria, Maleeha M; Lamers, Ideke J C IJ; Schmidts, Miriam M; Ajmal, Muhammad M; Jaffar, Sulman S; Ullah, Ehsan E; Mustafa, Bilal B; Ahmad, Shakeel S; Nazmutdinova, Katia K; Hoskins, Bethan B; van Wijk, Erwin E; Koster-Kamphuis, Linda L; Khan, Muhammad Imran MI; Beales, Phil L PL; Cremers, Frans P M FP; Roepman, Ronald R; Azam, Maleeha M; Arts, Heleen H HH; Qamar, Raheel R
Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies.
Scientific Reports
Tiwari, Amit A; Bahr, Angela A; Bähr, Luzy L; Fleischhauer, Johannes J; Zinkernagel, Martin S MS; Winkler, Niklas N; Barthelmes, Daniel D; Berger, Lieselotte L; Gerth-Kahlert, Christina C; Neidhardt, John J; Berger, Wolfgang W
Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mapping.
Journal Of Medical Genetics
Harville, H M HM; Held, S S; Diaz-Font, A A; Davis, E E EE; Diplas, B H BH; Lewis, R A RA; Borochowitz, Z U ZU; Zhou, W W; Chaki, M M; MacDonald, J J; Kayserili, H H; Beales, P L PL; Katsanis, N N; Otto, E E; Hildebrandt, F F