BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 33994118)

  • 1. Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.
    Wang T; Zhang Y; Liu L; Wang Y; Chen H; Fan T; Li J; Xia K; Sun Z
    J Genet Genomics; 2021 Apr; 48(4):312-323. PubMed ID: 33994118
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
    Zhang Y; Wang T; Wang Y; Xia K; Li J; Sun Z
    Mol Neurobiol; 2021 Aug; 58(8):3863-3873. PubMed ID: 33860439
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
    Wang L; Zhang Y; Li K; Wang Z; Wang X; Li B; Zhao G; Fang Z; Ling Z; Luo T; Xia L; Li Y; Guo H; Hu Z; Li J; Sun Z; Xia K
    Mol Autism; 2020 Oct; 11(1):75. PubMed ID: 33023636
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
    Gillentine MA; Wang T; Hoekzema K; Rosenfeld J; Liu P; Guo H; Kim CN; De Vries BBA; Vissers LELM; Nordenskjold M; Kvarnung M; Lindstrand A; Nordgren A; Gecz J; Iascone M; Cereda A; Scatigno A; Maitz S; Zanni G; Bertini E; Zweier C; Schuhmann S; Wiesener A; Pepper M; Panjwani H; Torti E; Abid F; Anselm I; Srivastava S; Atwal P; Bacino CA; Bhat G; Cobian K; Bird LM; Friedman J; Wright MS; Callewaert B; Petit F; Mathieu S; Afenjar A; Christensen CK; White KM; Elpeleg O; Berger I; Espineli EJ; Fagerberg C; Brasch-Andersen C; Hansen LK; Feyma T; Hughes S; Thiffault I; Sullivan B; Yan S; Keller K; Keren B; Mignot C; Kooy F; Meuwissen M; Basinger A; Kukolich M; Philips M; Ortega L; Drummond-Borg M; Lauridsen M; Sorensen K; Lehman A; ; Lopez-Rangel E; Levy P; Lessel D; Lotze T; Madan-Khetarpal S; Sebastian J; Vento J; Vats D; Benman LM; Mckee S; Mirzaa GM; Muss C; Pappas J; Peeters H; Romano C; Elia M; Galesi O; Simon MEH; van Gassen KLI; Simpson K; Stratton R; Syed S; Thevenon J; Palafoll IV; Vitobello A; Bournez M; Faivre L; Xia K; ; Earl RK; Nowakowski T; Bernier RA; Eichler EE
    Genome Med; 2021 Apr; 13(1):63. PubMed ID: 33874999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders.
    Li B; Li K; Tian D; Zhou Q; Xie Y; Fang Z; Wang X; Luo T; Wang Z; Zhang Y; Wang Y; Chen Q; Meng Q; Zhao G; Li J
    J Mol Med (Berl); 2020 Dec; 98(12):1701-1712. PubMed ID: 33047154
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
    Li J; Wang L; Guo H; Shi L; Zhang K; Tang M; Hu S; Dong S; Liu Y; Wang T; Yu P; He X; Hu Z; Zhao J; Liu C; Sun ZS; Xia K
    Mol Psychiatry; 2017 Sep; 22(9):1282-1290. PubMed ID: 28831199
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.
    McKenna B; Koomar T; Vervier K; Kremsreiter J; Michaelson JJ
    Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559312
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
    Mirzaa GM; Chong JX; Piton A; Popp B; Foss K; Guo H; Harripaul R; Xia K; Scheck J; Aldinger KA; Sajan SA; Tang S; Bonneau D; Beck A; White J; Mahida S; Harris J; Smith-Hicks C; Hoyer J; Zweier C; Reis A; Thiel CT; Jamra RA; Zeid N; Yang A; Farach LS; Walsh L; Payne K; Rohena L; Velinov M; Ziegler A; Schaefer E; Gatinois V; Geneviève D; Simon MEH; Kohler J; Rotenberg J; Wheeler P; Larson A; Ernst ME; Akman CI; Westman R; Blanchet P; Schillaci LA; Vincent-Delorme C; Gripp KW; Mattioli F; Guyader GL; Gerard B; Mathieu-Dramard M; Morin G; Sasanfar R; Ayub M; Vasli N; Yang S; Person R; Monaghan KG; Nickerson DA; van Binsbergen E; Enns GM; Dries AM; Rowe LJ; Tsai ACH; Svihovec S; Friedman J; Agha Z; Qamar R; Rodan LH; Martinez-Agosto J; Ockeloen CW; Vincent M; Sunderland WJ; Bernstein JA; ; Eichler EE; Vincent JB; ; Bamshad MJ
    Genet Med; 2020 Mar; 22(3):538-546. PubMed ID: 31723249
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
    Marcogliese PC; Deal SL; Andrews J; Harnish JM; Bhavana VH; Graves HK; Jangam S; Luo X; Liu N; Bei D; Chao YH; Hull B; Lee PT; Pan H; Bhadane P; Huang MC; Longley CM; Chao HT; Chung HL; Haelterman NA; Kanca O; Manivannan SN; Rossetti LZ; German RJ; Gerard A; Schwaibold EMC; Fehr S; Guerrini R; Vetro A; England E; Murali CN; Barakat TS; van Dooren MF; Wilke M; van Slegtenhorst M; Lesca G; Sabatier I; Chatron N; Brownstein CA; Madden JA; Agrawal PB; Keren B; Courtin T; Perrin L; Brugger M; Roser T; Leiz S; Mau-Them FT; Delanne J; Sukarova-Angelovska E; Trajkova S; Rosenhahn E; Strehlow V; Platzer K; Keller R; Pavinato L; Brusco A; Rosenfeld JA; Marom R; Wangler MF; Yamamoto S
    Cell Rep; 2022 Mar; 38(11):110517. PubMed ID: 35294868
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders.
    Pang N; Li K; Tan S; Chen M; He F; Chen C; Yang L; Zhang C; Deng X; Yang L; Mao L; Wang G; Duan H; Wang X; Zhang W; Guo H; Peng J; Yin F; Xia K
    Gene; 2024 Mar; 897():148071. PubMed ID: 38081334
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.
    Richter M; Murtaza N; Scharrenberg R; White SH; Johanns O; Walker S; Yuen RKC; Schwanke B; Bedürftig B; Henis M; Scharf S; Kraus V; Dörk R; Hellmann J; Lindenmaier Z; Ellegood J; Hartung H; Kwan V; Sedlacik J; Fiehler J; Schweizer M; Lerch JP; Hanganu-Opatz IL; Morellini F; Scherer SW; Singh KK; Calderon de Anda F
    Mol Psychiatry; 2019 Sep; 24(9):1329-1350. PubMed ID: 29467497
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.
    Zhao W; Tan J; Zhu T; Ou J; Li Y; Shen L; Wu H; Han L; Liu Y; Jia X; Bai T; Li H; Ke X; Zhao J; Zou X; Hu Z; Guo H; Xia K
    J Genet Genomics; 2019 May; 46(5):247-257. PubMed ID: 31196716
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.
    Takata A; Miyake N; Tsurusaki Y; Fukai R; Miyatake S; Koshimizu E; Kushima I; Okada T; Morikawa M; Uno Y; Ishizuka K; Nakamura K; Tsujii M; Yoshikawa T; Toyota T; Okamoto N; Hiraki Y; Hashimoto R; Yasuda Y; Saitoh S; Ohashi K; Sakai Y; Ohga S; Hara T; Kato M; Nakamura K; Ito A; Seiwa C; Shirahata E; Osaka H; Matsumoto A; Takeshita S; Tohyama J; Saikusa T; Matsuishi T; Nakamura T; Tsuboi T; Kato T; Suzuki T; Saitsu H; Nakashima M; Mizuguchi T; Tanaka F; Mori N; Ozaki N; Matsumoto N
    Cell Rep; 2018 Jan; 22(3):734-747. PubMed ID: 29346770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
    Chow J; Jensen M; Amini H; Hormozdiari F; Penn O; Shifman S; Girirajan S; Hormozdiari F
    Genome Med; 2019 Oct; 11(1):65. PubMed ID: 31653223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort.
    Chen S; Xiong J; Chen B; Zhang C; Deng X; He F; Yang L; Chen C; Peng J; Yin F
    Clin Chim Acta; 2022 Jan; 524():179-186. PubMed ID: 34800434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
    Nguyen HT; Bryois J; Kim A; Dobbyn A; Huckins LM; Munoz-Manchado AB; Ruderfer DM; Genovese G; Fromer M; Xu X; Pinto D; Linnarsson S; Verhage M; Smit AB; Hjerling-Leffler J; Buxbaum JD; Hultman C; Sklar P; Purcell SM; Lage K; He X; Sullivan PF; Stahl EA
    Genome Med; 2017 Dec; 9(1):114. PubMed ID: 29262854
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
    Padhi EM; Hayeck TJ; Cheng Z; Chatterjee S; Mannion BJ; Byrska-Bishop M; Willems M; Pinson L; Redon S; Benech C; Uguen K; Audebert-Bellanger S; Le Marechal C; Férec C; Efthymiou S; Rahman F; Maqbool S; Maroofian R; Houlden H; Musunuri R; Narzisi G; Abhyankar A; Hunter RD; Akiyama J; Fries LE; Ng JK; Mehinovic E; Stong N; Allen AS; Dickel DE; Bernier RA; Gorkin DU; Pennacchio LA; Zody MC; Turner TN
    Hum Genomics; 2021 Jul; 15(1):44. PubMed ID: 34256850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Excess of RALGAPB de novo variants in neurodevelopmental disorders.
    Shah AA; Zhang G; Li K; Liu C; Kanhar AA; Wang M; Quan Y; Wu H; Shen L; Khan R; Chen G; Ou J; Hu Z; Xia K; Guo H
    Eur J Med Genet; 2020 Nov; 63(11):104041. PubMed ID: 32853829
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders.
    Prem S; Millonig JH; DiCicco-Bloom E
    Adv Neurobiol; 2020; 25():109-153. PubMed ID: 32578146
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants.
    Hamanaka K; Miyake N; Mizuguchi T; Miyatake S; Uchiyama Y; Tsuchida N; Sekiguchi F; Mitsuhashi S; Tsurusaki Y; Nakashima M; Saitsu H; Yamada K; Sakamoto M; Fukuda H; Ohori S; Saida K; Itai T; Azuma Y; Koshimizu E; Fujita A; Erturk B; Hiraki Y; Ch'ng GS; Kato M; Okamoto N; Takata A; Matsumoto N
    Genome Med; 2022 Apr; 14(1):40. PubMed ID: 35468861
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.