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 *

190 related articles for article (PubMed ID: 36481753)

  • 41. Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: I: feed efficiency and component traits.
    Zhang F; Wang Y; Mukiibi R; Chen L; Vinsky M; Plastow G; Basarab J; Stothard P; Li C
    BMC Genomics; 2020 Jan; 21(1):36. PubMed ID: 31931702
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Gene-based association study of rare variants in children of diverse ancestries implicates TNFRSF21 in the development of allergic asthma.
    Clay S; Alladina J; Smith NP; Visness CM; Wood RA; O'Connor GT; Cohen RT; Khurana Hershey GK; Kercsmar CM; Gruchalla RS; Gill MA; Liu AH; Kim H; Kattan M; Bacharier LB; Rastogi D; Rivera-Spoljaric K; Robison RG; Gergen PJ; Busse WW; Villani AC; Cho JL; Medoff BD; Gern JE; Jackson DJ; Ober C; Dapas M
    J Allergy Clin Immunol; 2024 Mar; 153(3):809-820. PubMed ID: 37944567
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
    Sarnowski C; Leong A; Raffield LM; Wu P; de Vries PS; DiCorpo D; Guo X; Xu H; Liu Y; Zheng X; Hu Y; Brody JA; Goodarzi MO; Hidalgo BA; Highland HM; Jain D; Liu CT; Naik RP; O'Connell JR; Perry JA; Porneala BC; Selvin E; Wessel J; Psaty BM; Curran JE; Peralta JM; Blangero J; Kooperberg C; Mathias R; Johnson AD; Reiner AP; Mitchell BD; Cupples LA; Vasan RS; Correa A; Morrison AC; Boerwinkle E; Rotter JI; Rich SS; Manning AK; Dupuis J; Meigs JB; ; ; ;
    Am J Hum Genet; 2019 Oct; 105(4):706-718. PubMed ID: 31564435
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
    Li X; Chen H; Selvaraj MS; Van Buren E; Zhou H; Wang Y; Sun R; McCaw ZR; Yu Z; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Brody JA; Cade BE; Carson AP; Carlson JC; Chami N; Chen YI; Curran JE; de Vries PS; Fornage M; Franceschini N; Freedman BI; Gu C; Heard-Costa NL; He J; Hou L; Hung YJ; Irvin MR; Kaplan RC; Kardia SLR; Kelly T; Konigsberg I; Kooperberg C; Kral BG; Li C; Loos RJF; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Palmer ND; Peyser PA; Psaty BM; Raffield LM; Redline S; Reiner AP; Rich SS; Sitlani CM; Smith JA; Taylor KD; Tiwari H; Vasan RS; Wang Z; Yanek LR; Yu B; ; Rice KM; Rotter JI; Peloso GM; Natarajan P; Li Z; Liu Z; Lin X
    bioRxiv; 2023 Nov; ():. PubMed ID: 37961350
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
    Hodonsky CJ; Baldassari AR; Bien SA; Raffield LM; Highland HM; Sitlani CM; Wojcik GL; Tao R; Graff M; Tang W; Thyagarajan B; Buyske S; Fornage M; Hindorff LA; Li Y; Lin D; Reiner AP; North KE; Loos RJF; Kooperberg C; Avery CL
    BMC Genomics; 2020 Mar; 21(1):228. PubMed ID: 32171239
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.
    Peljto AL; Blumhagen RZ; Walts AD; Cardwell J; Powers J; Corte TJ; Dickinson JL; Glaspole I; Moodley YP; Vasakova MK; Bendstrup E; Davidsen JR; Borie R; Crestani B; Dieude P; Bonella F; Costabel U; Gudmundsson G; Donnelly SC; Egan J; Henry MT; Keane MP; Kennedy MP; McCarthy C; McElroy AN; Olaniyi JA; O'Reilly KMA; Richeldi L; Leone PM; Poletti V; Puppo F; Tomassetti S; Luzzi V; Kokturk N; Mogulkoc N; Fiddler CA; Hirani N; Jenkins RG; Maher TM; Molyneaux PL; Parfrey H; Braybrooke R; Blackwell TS; Jackson PD; Nathan SD; Porteous MK; Brown KK; Christie JD; Collard HR; Eickelberg O; Foster EE; Gibson KF; Glassberg M; Kass DJ; Kropski JA; Lederer D; Linderholm AL; Loyd J; Mathai SK; Montesi SB; Noth I; Oldham JM; Palmisciano AJ; Reichner CA; Rojas M; Roman J; Schluger N; Shea BS; Swigris JJ; Wolters PJ; Zhang Y; Prele CMA; Enghelmayer JI; Otaola M; Ryerson CJ; Salinas M; Sterclova M; Gebremariam TH; Myllärniemi M; Carbone RG; Furusawa H; Hirose M; Inoue Y; Miyazaki Y; Ohta K; Ohta S; Okamoto T; Kim DS; Pardo A; Selman M; Aranda AU; Park MS; Park JS; Song JW; Molina-Molina M; Planas-Cerezales L; Westergren-Thorsson G; Smith AV; Manichaikul AW; Kim JS; Rich SS; Oelsner EC; Barr RG; Rotter JI; Dupuis J; O'Connor G; Vasan RS; Cho MH; Silverman EK; Schwarz MI; Steele MP; Lee JS; Yang IV; Fingerlin TE; Schwartz DA
    Am J Respir Crit Care Med; 2023 May; 207(9):1194-1202. PubMed ID: 36602845
    [No Abstract]   [Full Text] [Related]  

  • 47. FunSPU: A versatile and adaptive multiple functional annotation-based association test of whole-genome sequencing data.
    Ma Y; Wei P
    PLoS Genet; 2019 Apr; 15(4):e1008081. PubMed ID: 31034468
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.
    Wen J; Xie M; Rowland B; Rosen JD; Sun Q; Chen J; Tapia AL; Qian H; Kowalski MH; Shan Y; Young KL; Graff M; Argos M; Avery CL; Bien SA; Buyske S; Yin J; Choquet H; Fornage M; Hodonsky CJ; Jorgenson E; Kooperberg C; Loos RJF; Liu Y; Moon JY; North KE; Rich SS; Rotter JI; Smith JA; Zhao W; Shang L; Wang T; Zhou X; Reiner AP; Raffield LM; Li Y
    Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356065
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
    Raffield LM; Iyengar AK; Wang B; Gaynor SM; Spracklen CN; Zhong X; Kowalski MH; Salimi S; Polfus LM; Benjamin EJ; Bis JC; Bowler R; Cade BE; Choi WJ; Comellas AP; Correa A; Cruz P; Doddapaneni H; Durda P; Gogarten SM; Jain D; Kim RW; Kral BG; Lange LA; Larson MG; Laurie C; Lee J; Lee S; Lewis JP; Metcalf GA; Mitchell BD; Momin Z; Muzny DM; Pankratz N; Park CJ; Rich SS; Rotter JI; Ryan K; Seo D; Tracy RP; Viaud-Martinez KA; Yanek LR; Zhao LP; Lin X; Li B; Li Y; Dupuis J; Reiner AP; Mohlke KL; Auer PL; ;
    Am J Hum Genet; 2020 Jan; 106(1):112-120. PubMed ID: 31883642
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Spontaneous preterm birth: advances toward the discovery of genetic predisposition.
    Strauss JF; Romero R; Gomez-Lopez N; Haymond-Thornburg H; Modi BP; Teves ME; Pearson LN; York TP; Schenkein HA
    Am J Obstet Gynecol; 2018 Mar; 218(3):294-314.e2. PubMed ID: 29248470
    [TBL] [Abstract][Full Text] [Related]  

  • 51. eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing data.
    Yang Y; Sun Q; Huang L; Broome JG; Correa A; Reiner A; ; Raffield LM; Yang Y; Li Y
    Brief Bioinform; 2022 Jan; 23(1):. PubMed ID: 34882196
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
    Wagner MJ
    Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.
    DiCorpo D; Gaynor SM; Russell EM; Westerman KE; Raffield LM; Majarian TD; Wu P; Sarnowski C; Highland HM; Jackson A; Hasbani NR; de Vries PS; Brody JA; Hidalgo B; Guo X; Perry JA; O'Connell JR; Lent S; Montasser ME; Cade BE; Jain D; Wang H; D'Oliveira Albanus R; Varshney A; Yanek LR; Lange L; Palmer ND; Almeida M; Peralta JM; Aslibekyan S; Baldridge AS; Bertoni AG; Bielak LF; Chen CS; Chen YI; Choi WJ; Goodarzi MO; Floyd JS; Irvin MR; Kalyani RR; Kelly TN; Lee S; Liu CT; Loesch D; Manson JE; Minster RL; Naseri T; Pankow JS; Rasmussen-Torvik LJ; Reiner AP; Reupena MS; Selvin E; Smith JA; Weeks DE; Xu H; Yao J; Zhao W; Parker S; Alonso A; Arnett DK; Blangero J; Boerwinkle E; Correa A; Cupples LA; Curran JE; Duggirala R; He J; Heckbert SR; Kardia SLR; Kim RW; Kooperberg C; Liu S; Mathias RA; McGarvey ST; Mitchell BD; Morrison AC; Peyser PA; Psaty BM; Redline S; Shuldiner AR; Taylor KD; Vasan RS; Viaud-Martinez KA; Florez JC; Wilson JG; Sladek R; Rich SS; Rotter JI; Lin X; Dupuis J; Meigs JB; Wessel J; Manning AK
    Commun Biol; 2022 Jul; 5(1):756. PubMed ID: 35902682
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
    Prokopenko D; Sakornsakolpat P; Fier HL; Qiao D; Parker MM; McDonald MN; Manichaikul A; Rich SS; Barr RG; Williams CJ; Brantly ML; Lange C; Beaty TH; Crapo JD; Silverman EK; Cho MH
    Am J Respir Cell Mol Biol; 2018 Nov; 59(5):614-622. PubMed ID: 29949718
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population.
    Mauleekoonphairoj J; Tongsima S; Khongphatthanayothin A; Jurgens SJ; Zimmerman DS; Sutjaporn B; Wandee P; Bezzina CR; Nademanee K; Poovorawan Y
    Sci Rep; 2023 Jul; 13(1):12360. PubMed ID: 37524845
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
    Li X; Li Z; Zhou H; Gaynor SM; Liu Y; Chen H; Sun R; Dey R; Arnett DK; Aslibekyan S; Ballantyne CM; Bielak LF; Blangero J; Boerwinkle E; Bowden DW; Broome JG; Conomos MP; Correa A; Cupples LA; Curran JE; Freedman BI; Guo X; Hindy G; Irvin MR; Kardia SLR; Kathiresan S; Khan AT; Kooperberg CL; Laurie CC; Liu XS; Mahaney MC; Manichaikul AW; Martin LW; Mathias RA; McGarvey ST; Mitchell BD; Montasser ME; Moore JE; Morrison AC; O'Connell JR; Palmer ND; Pampana A; Peralta JM; Peyser PA; Psaty BM; Redline S; Rice KM; Rich SS; Smith JA; Tiwari HK; Tsai MY; Vasan RS; Wang FF; Weeks DE; Weng Z; Wilson JG; Yanek LR; ; ; Neale BM; Sunyaev SR; Abecasis GR; Rotter JI; Willer CJ; Peloso GM; Natarajan P; Lin X
    Nat Genet; 2020 Sep; 52(9):969-983. PubMed ID: 32839606
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens.
    Morris JA; Caragine C; Daniloski Z; Domingo J; Barry T; Lu L; Davis K; Ziosi M; Glinos DA; Hao S; Mimitou EP; Smibert P; Roeder K; Katsevich E; Lappalainen T; Sanjana NE
    Science; 2023 May; 380(6646):eadh7699. PubMed ID: 37141313
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
    Rhodes CJ; Batai K; Bleda M; Haimel M; Southgate L; Germain M; Pauciulo MW; Hadinnapola C; Aman J; Girerd B; Arora A; Knight J; Hanscombe KB; Karnes JH; Kaakinen M; Gall H; Ulrich A; Harbaum L; Cebola I; Ferrer J; Lutz K; Swietlik EM; Ahmad F; Amouyel P; Archer SL; Argula R; Austin ED; Badesch D; Bakshi S; Barnett C; Benza R; Bhatt N; Bogaard HJ; Burger CD; Chakinala M; Church C; Coghlan JG; Condliffe R; Corris PA; Danesino C; Debette S; Elliott CG; Elwing J; Eyries M; Fortin T; Franke A; Frantz RP; Frost A; Garcia JGN; Ghio S; Ghofrani HA; Gibbs JSR; Harley J; He H; Hill NS; Hirsch R; Houweling AC; Howard LS; Ivy D; Kiely DG; Klinger J; Kovacs G; Lahm T; Laudes M; Machado RD; MacKenzie Ross RV; Marsolo K; Martin LJ; Moledina S; Montani D; Nathan SD; Newnham M; Olschewski A; Olschewski H; Oudiz RJ; Ouwehand WH; Peacock AJ; Pepke-Zaba J; Rehman Z; Robbins I; Roden DM; Rosenzweig EB; Saydain G; Scelsi L; Schilz R; Seeger W; Shaffer CM; Simms RW; Simon M; Sitbon O; Suntharalingam J; Tang H; Tchourbanov AY; Thenappan T; Torres F; Toshner MR; Treacy CM; Vonk Noordegraaf A; Waisfisz Q; Walsworth AK; Walter RE; Wharton J; White RJ; Wilt J; Wort SJ; Yung D; Lawrie A; Humbert M; Soubrier F; Trégouët DA; Prokopenko I; Kittles R; Gräf S; Nichols WC; Trembath RC; Desai AA; Morrell NW; Wilkins MR; ; ;
    Lancet Respir Med; 2019 Mar; 7(3):227-238. PubMed ID: 30527956
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Extreme Trait Whole-Genome Sequencing Identifies PTPRO as a Novel Candidate Gene in Emphysema with Severe Airflow Obstruction.
    Radder JE; Zhang Y; Gregory AD; Yu S; Kelly NJ; Leader JK; Kaminski N; Sciurba FC; Shapiro SD
    Am J Respir Crit Care Med; 2017 Jul; 196(2):159-171. PubMed ID: 28199135
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Sequence variants in three loci influence monocyte counts and erythrocyte volume.
    Ferreira MA; Hottenga JJ; Warrington NM; Medland SE; Willemsen G; Lawrence RW; Gordon S; de Geus EJ; Henders AK; Smit JH; Campbell MJ; Wallace L; Evans DM; Wright MJ; Nyholt DR; James AL; Beilby JP; Penninx BW; Palmer LJ; Frazer IH; Montgomery GW; Martin NG; Boomsma DI
    Am J Hum Genet; 2009 Nov; 85(5):745-9. PubMed ID: 19853236
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.