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 *

209 related articles for article (PubMed ID: 38154517)

  • 1. Identification of novel rare variants for anxiety: an exome-wide association study in the UK Biobank.
    Pan C; Cheng S; Liu L; Chen Y; Meng P; Yang X; Li C; Zhang J; Zhang Z; Zhang H; Cheng B; Wen Y; Jia Y; Zhang F
    Prog Neuropsychopharmacol Biol Psychiatry; 2024 Mar; 130():110928. PubMed ID: 38154517
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluating the role of rare genetic variation in sleep duration.
    Meng P; Pan C; Cheng S; Li C; Yao Y; Liu L; Cheng B; Yang X; Zhang Z; Chen Y; Zhang J; Zhang H; Wen Y; Jia Y; Guo X; Zhang F
    Sleep Health; 2022 Oct; 8(5):536-541. PubMed ID: 35907708
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome-wide screening identifies novel rare risk variants for major depression disorder.
    Cheng S; Cheng B; Liu L; Yang X; Meng P; Yao Y; Pan C; Zhang J; Li C; Zhang H; Chen Y; Zhang Z; Wen Y; Jia Y; Zhang F
    Mol Psychiatry; 2022 Jul; 27(7):3069-3074. PubMed ID: 35365804
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression.
    Tian R; Ge T; Kweon H; Rocha DB; Lam M; Liu JZ; Singh K; ; Levey DF; Gelernter J; Stein MB; Tsai EA; Huang H; Chabris CF; Lencz T; Runz H; Chen CY
    Nat Commun; 2024 Feb; 15(1):1755. PubMed ID: 38409228
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome-wide screening identifies novel rare risk variants for bone mineral density.
    He D; Pan C; Zhao Y; Wei W; Qin X; Cai Q; Shi S; Chu X; Zhang N; Jia Y; Wen Y; Cheng B; Liu H; Feng R; Zhang F; Xu P
    Osteoporos Int; 2023 May; 34(5):965-975. PubMed ID: 36849660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
    Brazel DM; Jiang Y; Hughey JM; Turcot V; Zhan X; Gong J; Batini C; Weissenkampen JD; Liu M; ; ; Barnes DR; Bertelsen S; Chou YL; Erzurumluoglu AM; Faul JD; Haessler J; Hammerschlag AR; Hsu C; Kapoor M; Lai D; Le N; de Leeuw CA; Loukola A; Mangino M; Melbourne CA; Pistis G; Qaiser B; Rohde R; Shao Y; Stringham H; Wetherill L; Zhao W; Agrawal A; Bierut L; Chen C; Eaton CB; Goate A; Haiman C; Heath A; Iacono WG; Martin NG; Polderman TJ; Reiner A; Rice J; Schlessinger D; Scholte HS; Smith JA; Tardif JC; Tindle HA; van der Leij AR; Boehnke M; Chang-Claude J; Cucca F; David SP; Foroud T; Howson JMM; Kardia SLR; Kooperberg C; Laakso M; Lettre G; Madden P; McGue M; North K; Posthuma D; Spector T; Stram D; Tobin MD; Weir DR; Kaprio J; Abecasis GR; Liu DJ; Vrieze S
    Biol Psychiatry; 2019 Jun; 85(11):946-955. PubMed ID: 30679032
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
    Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
    JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Efficient identification of trait-associated loss-of-function variants in the UK Biobank cohort by exome-sequencing based genotype imputation.
    Yu WY; Yan SS; Zhang SH; Ni JJ; Bin-Li ; Pei YF; Zhang L
    Genet Epidemiol; 2023 Mar; 47(2):121-134. PubMed ID: 36490288
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
    Ahluwalia TS; Schulz CA; Waage J; Skaaby T; Sandholm N; van Zuydam N; Charmet R; Bork-Jensen J; Almgren P; Thuesen BH; Bedin M; Brandslund I; Christensen CK; Linneberg A; Ahlqvist E; Groop PH; Hadjadj S; Tregouet DA; Jørgensen ME; Grarup N; Pedersen O; Simons M; Groop L; Orho-Melander M; McCarthy MI; Melander O; Rossing P; Kilpeläinen TO; Hansen T
    Diabetologia; 2019 Feb; 62(2):292-305. PubMed ID: 30547231
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
    Toma C; Shaw AD; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM
    J Psychiatry Neurosci; 2021 Mar; 46(2):E247-E257. PubMed ID: 33729739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
    Barton AR; Sherman MA; Mukamel RE; Loh PR
    Nat Genet; 2021 Aug; 53(8):1260-1269. PubMed ID: 34226706
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare variant contribution to human disease in 281,104 UK Biobank exomes.
    Wang Q; Dhindsa RS; Carss K; Harper AR; Nag A; Tachmazidou I; Vitsios D; Deevi SVV; Mackay A; Muthas D; Hühn M; Monkley S; Olsson H; ; Wasilewski S; Smith KR; March R; Platt A; Haefliger C; Petrovski S
    Nature; 2021 Sep; 597(7877):527-532. PubMed ID: 34375979
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrated gene-based and pathway analyses using UK Biobank data identify novel genes for chronic respiratory diseases.
    Wang L; Fang R; Zhu M; Qin N; Wang Y; Fan J; Sun Q; Ji M; Fan X; Xie J; Ma H; Dai J
    Gene; 2021 Jan; 767():145287. PubMed ID: 33181258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole exome sequencing of extreme age-related macular degeneration phenotypes.
    Sardell RJ; Bailey JN; Courtenay MD; Whitehead P; Laux RA; Adams LD; Fortun JA; Brantley MA; Kovach JL; Schwartz SG; Agarwal A; Scott WK; Haines JL; Pericak-Vance MA
    Mol Vis; 2016; 22():1062-76. PubMed ID: 27625572
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank.
    Lassen FH; Venkatesh SS; Baya N; Hill B; Zhou W; Bloemendal A; Neale BM; Kessler BM; Whiffin N; Lindgren CM; Palmer DS
    Cell Genom; 2024 Jul; 4(7):100602. PubMed ID: 38944039
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia risk.
    Curtis D
    J Hum Genet; 2024 Jun; 69(6):255-262. PubMed ID: 38454133
    [TBL] [Abstract][Full Text] [Related]  

  • 18. UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.
    Zhao Z; Bi W; Zhou W; VandeHaar P; Fritsche LG; Lee S
    Am J Hum Genet; 2020 Jan; 106(1):3-12. PubMed ID: 31866045
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Family-based exome sequencing identifies rare coding variants in age-related macular degeneration.
    Ratnapriya R; Acar İE; Geerlings MJ; Branham K; Kwong A; Saksens NTM; Pauper M; Corominas J; Kwicklis M; Zipprer D; Starostik MR; Othman M; Yashar B; Abecasis GR; Chew EY; Ferrington DA; Hoyng CB; Swaroop A; den Hollander AI
    Hum Mol Genet; 2020 Jul; 29(12):2022-2034. PubMed ID: 32246154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank.
    Nag A; Dhindsa RS; Middleton L; Jiang X; Vitsios D; Wigmore E; Allman EL; Reznichenko A; Carss K; Smith KR; Wang Q; Challis B; Paul DS; Harper AR; Petrovski S
    Am J Hum Genet; 2023 Mar; 110(3):487-498. PubMed ID: 36809768
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.