These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

304 related articles for article (PubMed ID: 29531218)

  • 21. Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing.
    Toma C; Díaz-Gay M; Soares de Lima Y; Arnau-Collell C; Franch-Expósito S; Muñoz J; Overs B; Bonjoch L; Carballal S; Ocaña T; Cuatrecasas M; Díaz de Bustamante A; Castells A; Bujanda L; Cubiella J; Balaguer F; Rodríguez-Alcalde D; Fullerton JM; Castellví-Bel S
    Clin Transl Gastroenterol; 2019 Oct; 10(10):e00100. PubMed ID: 31663907
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.
    Lindholm Carlström E; Halvardson J; Etemadikhah M; Wetterberg L; Gustavson KH; Feuk L
    BMC Med Genomics; 2019 Nov; 12(1):156. PubMed ID: 31694657
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Haplotype phasing of a bipolar disorder pedigree revealed rare multiple mutations of SPOCD1 gene in the 1p36-35 susceptibility locus.
    Takamatsu G; Yanagi K; Koganebuchi K; Yoshida F; Lee JS; Toyama K; Hattori K; Katagiri C; Kondo T; Kunugi H; Kimura R; Kaname T; Matsushita M
    J Affect Disord; 2022 Aug; 310():96-105. PubMed ID: 35504398
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
    Jia X; Goes FS; Locke AE; Palmer D; Wang W; Cohen-Woods S; Genovese G; Jackson AU; Jiang C; Kvale M; Mullins N; Nguyen H; Pirooznia M; Rivera M; Ruderfer DM; Shen L; Thai K; Zawistowski M; Zhuang Y; Abecasis G; Akil H; Bergen S; Burmeister M; Chapman S; DelaBastide M; Juréus A; Kang HM; Kwok PY; Li JZ; Levy SE; Monson ET; Moran J; Sobell J; Watson S; Willour V; Zöllner S; Adolfsson R; Blackwood D; Boehnke M; Breen G; Corvin A; Craddock N; DiFlorio A; Hultman CM; Landen M; Lewis C; McCarroll SA; Richard McCombie W; McGuffin P; McIntosh A; McQuillin A; Morris D; Myers RM; O'Donovan M; Ophoff R; Boks M; Kahn R; Ouwehand W; Owen M; Pato C; Pato M; Posthuma D; Potash JB; Reif A; Sklar P; Smoller J; Sullivan PF; Vincent J; Walters J; Neale B; Purcell S; Risch N; Schaefer C; Stahl EA; Zandi PP; Scott LJ
    Mol Psychiatry; 2021 Sep; 26(9):5239-5250. PubMed ID: 33483695
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.
    John J; Sharma A; Kukshal P; Bhatia T; Nimgaonkar VL; Deshpande SN; Thelma BK
    Schizophr Bull; 2019 Jan; 45(1):256-263. PubMed ID: 29385606
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
    Bureau A; Parker MM; Ruczinski I; Taub MA; Marazita ML; Murray JC; Mangold E; Noethen MM; Ludwig KU; Hetmanski JB; Bailey-Wilson JE; Cropp CD; Li Q; Szymczak S; Albacha-Hejazi H; Alqosayer K; Field LL; Wu-Chou YH; Doheny KF; Ling H; Scott AF; Beaty TH
    Genetics; 2014 Jul; 197(3):1039-44. PubMed ID: 24793288
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
    Corominas J; Klein M; Zayats T; Rivero O; Ziegler GC; Pauper M; Neveling K; Poelmans G; Jansch C; Svirin E; Geissler J; Weber H; Reif A; Arias Vasquez A; Galesloot TE; Kiemeney LALM; Buitelaar JK; Ramos-Quiroga JA; Cormand B; Ribasés M; Hveem K; Gabrielsen ME; Hoffmann P; Cichon S; Haavik J; Johansson S; Jacob CP; Romanos M; Franke B; Lesch KP
    Mol Psychiatry; 2020 Sep; 25(9):2047-2057. PubMed ID: 30116028
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families.
    Fazia T; Marzanati D; Carotenuto AL; Beecham A; Hadjixenofontos A; McCauley JL; Saddi V; Piras M; Bernardinelli L; Gentilini D
    Curr Issues Mol Biol; 2021 Oct; 43(3):1778-1793. PubMed ID: 34889895
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haplotype phasing and inheritance of copy number variants in nuclear families.
    Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M
    PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families.
    Pan J; Ma S; Teng Y; Liang D; Li Z; Wu L
    Clin Chim Acta; 2022 Jul; 532():53-60. PubMed ID: 35640668
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.
    Sul JH; Service SK; Huang AY; Ramensky V; Hwang SG; Teshiba TM; Park Y; Ori APS; Zhang Z; Mullins N; Olde Loohuis LM; Fears SC; Araya C; Araya X; Spesny M; Bejarano J; Ramirez M; Castrillón G; Gomez-Makhinson J; Lopez MC; Montoya G; Montoya CP; Aldana I; Escobar JI; Ospina-Duque J; Kremeyer B; Bedoya G; Ruiz-Linares A; Cantor RM; Molina J; Coppola G; Ophoff RA; Macaya G; Lopez-Jaramillo C; Reus V; Bearden CE; Sabatti C; Freimer NB
    Transl Psychiatry; 2020 Feb; 10(1):74. PubMed ID: 32094344
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
    Badner JA; Koller D; Foroud T; Edenberg H; Nurnberger JI; Zandi PP; Willour VL; McMahon FJ; Potash JB; Hamshere M; Grozeva D; Green E; Kirov G; Jones I; Jones L; Craddock N; Morris D; Segurado R; Gill M; Sadovnick D; Remick R; Keck P; Kelsoe J; Ayub M; MacLean A; Blackwood D; Liu CY; Gershon ES; McMahon W; Lyon GJ; Robinson R; Ross J; Byerley W
    Mol Psychiatry; 2012 Jul; 17(8):818-26. PubMed ID: 21769101
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
    Pizzo L; Jensen M; Polyak A; Rosenfeld JA; Mannik K; Krishnan A; McCready E; Pichon O; Le Caignec C; Van Dijck A; Pope K; Voorhoeve E; Yoon J; Stankiewicz P; Cheung SW; Pazuchanics D; Huber E; Kumar V; Kember RL; Mari F; Curró A; Castiglia L; Galesi O; Avola E; Mattina T; Fichera M; Mandarà L; Vincent M; Nizon M; Mercier S; Bénéteau C; Blesson S; Martin-Coignard D; Mosca-Boidron AL; Caberg JH; Bucan M; Zeesman S; Nowaczyk MJM; Lefebvre M; Faivre L; Callier P; Skinner C; Keren B; Perrine C; Prontera P; Marle N; Renieri A; Reymond A; Kooy RF; Isidor B; Schwartz C; Romano C; Sistermans E; Amor DJ; Andrieux J; Girirajan S
    Genet Med; 2019 Apr; 21(4):816-825. PubMed ID: 30190612
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.
    Chang YS; Lin CY; Huang HY; Chang JG; Kuo HT
    Mol Genet Genomic Med; 2019 Dec; 7(12):e996. PubMed ID: 31595719
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe.
    Wormser O; Gradstein L; Kadar E; Yogev Y; Perez Y; Mashkit E; Elbedour K; Drabkin M; Markus B; Kadir R; Halperin D; Khalaila S; Levy J; Lifshitz T; Manor E; Birk OS
    Am J Med Genet A; 2018 Dec; 176(12):2695-2703. PubMed ID: 30513137
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families.
    Fatima A; Abdullah U; Farooq M; Mang Y; Mehrjouy MM; Asif M; Ali Z; Tommerup N; Baig SM
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946848
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
    Bacchelli E; Cameli C; Viggiano M; Igliozzi R; Mancini A; Tancredi R; Battaglia A; Maestrini E
    Sci Rep; 2020 Feb; 10(1):3198. PubMed ID: 32081867
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder.
    Khan H; Harripaul R; Mikhailov A; Herzi S; Bowers S; Ayub M; Shabbir MI; Vincent JB
    Sci Rep; 2024 Apr; 14(1):9230. PubMed ID: 38649688
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
    Noor A; Lionel AC; Cohen-Woods S; Moghimi N; Rucker J; Fennell A; Thiruvahindrapuram B; Kaufman L; Degagne B; Wei J; Parikh SV; Muglia P; Forte J; Scherer SW; Kennedy JL; Xu W; McGuffin P; Farmer A; Strauss J; Vincent JB
    Am J Med Genet B Neuropsychiatr Genet; 2014 Jun; 165B(4):303-13. PubMed ID: 24700553
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole genome sequencing and rare variant analysis in essential tremor families.
    Odgerel Z; Sonti S; Hernandez N; Park J; Ottman R; Louis ED; Clark LN
    PLoS One; 2019; 14(8):e0220512. PubMed ID: 31404076
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.