BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 30671673)

  • 1. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
    He KY; Li X; Kelly TN; Liang J; Cade BE; Assimes TL; Becker LC; Beitelshees AL; Bress AP; Chang YC; Chen YI; de Vries PS; Fox ER; Franceschini N; Furniss A; Gao Y; Guo X; Haessler J; Hwang SJ; Irvin MR; Kalyani RR; Liu CT; Liu C; Martin LW; Montasser ME; Muntner PM; Mwasongwe S; Palmas W; Reiner AP; Shimbo D; Smith JA; Snively BM; Yanek LR; Boerwinkle E; Correa A; Cupples LA; He J; Kardia SLR; Kooperberg C; Mathias RA; Mitchell BD; Psaty BM; Vasan RS; Rao DC; Rich SS; Rotter JI; Wilson JG; ; Chakravarti A; Morrison AC; Levy D; Arnett DK; Redline S; Zhu X
    Hum Genet; 2019 Feb; 138(2):199-210. PubMed ID: 30671673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
    He KY; Wang H; Cade BE; Nandakumar P; Giri A; Ware EB; Haessler J; Liang J; Smith JA; Franceschini N; Le TH; Kooperberg C; Edwards TL; Kardia SL; Lin X; Chakravarti A; Redline S; Zhu X
    PLoS Genet; 2017 Mar; 13(3):e1006678. PubMed ID: 28346479
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare coding variants in RCN3 are associated with blood pressure.
    He KY; Kelly TN; Wang H; Liang J; Zhu L; Cade BE; Assimes TL; Becker LC; Beitelshees AL; Bielak LF; Bress AP; Brody JA; Chang YC; Chang YC; de Vries PS; Duggirala R; Fox ER; Franceschini N; Furniss AL; Gao Y; Guo X; Haessler J; Hung YJ; Hwang SJ; Irvin MR; Kalyani RR; Liu CT; Liu C; Martin LW; Montasser ME; Muntner PM; Mwasongwe S; Naseri T; Palmas W; Reupena MS; Rice KM; Sheu WH; Shimbo D; Smith JA; Snively BM; Yanek LR; Zhao W; Blangero J; Boerwinkle E; Chen YI; Correa A; Cupples LA; Curran JE; Fornage M; He J; Hou L; Kaplan RC; Kardia SLR; Kenny EE; Kooperberg C; Lloyd-Jones D; Loos RJF; Mathias RA; McGarvey ST; Mitchell BD; North KE; Peyser PA; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Rotter JI; Taylor KD; Tracy R; Vasan RS; ; Morrison AC; Levy D; Chakravarti A; Arnett DK; Zhu X
    BMC Genomics; 2022 Feb; 23(1):148. PubMed ID: 35183128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
    Hu Y; Stilp AM; McHugh CP; Rao S; Jain D; Zheng X; Lane J; Méric de Bellefon S; Raffield LM; Chen MH; Yanek LR; Wheeler M; Yao Y; Ren C; Broome J; Moon JY; de Vries PS; Hobbs BD; Sun Q; Surendran P; Brody JA; Blackwell TW; Choquet H; Ryan K; Duggirala R; Heard-Costa N; Wang Z; Chami N; Preuss MH; Min N; Ekunwe L; Lange LA; Cushman M; Faraday N; Curran JE; Almasy L; Kundu K; Smith AV; Gabriel S; Rotter JI; Fornage M; Lloyd-Jones DM; Vasan RS; Smith NL; North KE; Boerwinkle E; Becker LC; Lewis JP; Abecasis GR; Hou L; O'Connell JR; Morrison AC; Beaty TH; Kaplan R; Correa A; Blangero J; Jorgenson E; Psaty BM; Kooperberg C; Walton RT; Kleinstiver BP; Tang H; Loos RJF; Soranzo N; Butterworth AS; Nickerson D; Rich SS; Mitchell BD; Johnson AD; Auer PL; Li Y; Mathias RA; Lettre G; Pankratz N; Laurie CC; Laurie CA; Bauer DE; Conomos MP; Reiner AP;
    Am J Hum Genet; 2021 May; 108(5):874-893. PubMed ID: 33887194
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.
    Hu Y; Haessler JW; Manansala R; Wiggins KL; Moscati A; Beiser A; Heard-Costa NL; Sarnowski C; Raffield LM; Chung J; Marini S; Anderson CD; Rosand J; Xu H; Sun X; Kelly TN; Wong Q; Lange LA; Rotter JI; Correa A; Vasan RS; Seshadri S; Rich SS; Do R; Loos RJF; Longstreth WT; Bis JC; Psaty BM; Tirschwell DL; Assimes TL; Silver B; Liu S; Jackson R; Wassertheil-Smoller S; Mitchell BD; Fornage M; Auer PL; Reiner AP; Kooperberg C;
    Stroke; 2022 Mar; 53(3):875-885. PubMed ID: 34727735
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
    Kowalski MH; Qian H; Hou Z; Rosen JD; Tapia AL; Shan Y; Jain D; Argos M; Arnett DK; Avery C; Barnes KC; Becker LC; Bien SA; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Buyske S; Cai J; Cho MH; Choi SH; Choquet H; Cupples LA; Cushman M; Daya M; de Vries PS; Ellinor PT; Faraday N; Fornage M; Gabriel S; Ganesh SK; Graff M; Gupta N; He J; Heckbert SR; Hidalgo B; Hodonsky CJ; Irvin MR; Johnson AD; Jorgenson E; Kaplan R; Kardia SLR; Kelly TN; Kooperberg C; Lasky-Su JA; Loos RJF; Lubitz SA; Mathias RA; McHugh CP; Montgomery C; Moon JY; Morrison AC; Palmer ND; Pankratz N; Papanicolaou GJ; Peralta JM; Peyser PA; Rich SS; Rotter JI; Silverman EK; Smith JA; Smith NL; Taylor KD; Thornton TA; Tiwari HK; Tracy RP; Wang T; Weiss ST; Weng LC; Wiggins KL; Wilson JG; Yanek LR; Zöllner S; North KE; Auer PL; ; ; Raffield LM; Reiner AP; Li Y
    PLoS Genet; 2019 Dec; 15(12):e1008500. PubMed ID: 31869403
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
    Lin BM; Grinde KE; Brody JA; Breeze CE; Raffield LM; Mychaleckyj JC; Thornton TA; Perry JA; Baier LJ; de Las Fuentes L; Guo X; Heavner BD; Hanson RL; Hung YJ; Qian H; Hsiung CA; Hwang SJ; Irvin MR; Jain D; Kelly TN; Kobes S; Lange L; Lash JP; Li Y; Liu X; Mi X; Musani SK; Papanicolaou GJ; Parsa A; Reiner AP; Salimi S; Sheu WH; Shuldiner AR; Taylor KD; Smith AV; Smith JA; Tin A; Vaidya D; Wallace RB; Yamamoto K; Sakaue S; Matsuda K; Kamatani Y; Momozawa Y; Yanek LR; Young BA; Zhao W; Okada Y; Abecasis G; Psaty BM; Arnett DK; Boerwinkle E; Cai J; Yii-Der Chen I; Correa A; Cupples LA; He J; Kardia SL; Kooperberg C; Mathias RA; Mitchell BD; Nickerson DA; Turner ST; Vasan RS; Rotter JI; Levy D; Kramer HJ; Köttgen A; Nhlbi Trans-Omics For Precision Medicine TOPMed Consortium ; TOPMed Kidney Working Group ; Rich SS; Lin DY; Browning SR; Franceschini N
    EBioMedicine; 2021 Jan; 63():103157. PubMed ID: 33418499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31.
    Wang H; Nandakumar P; Tekola-Ayele F; Tayo BO; Ware EB; Gu CC; Lu Y; Yao J; Zhao W; Smith JA; Hellwege JN; Guo X; Edwards TL; Loos RJF; Arnett DK; Fornage M; Rotimi C; Kardia SLR; Cooper RS; Rao DC; Ehret G; Chakravarti A; Zhu X
    Eur J Hum Genet; 2019 Feb; 27(2):269-277. PubMed ID: 30262922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
    Huerta-Chagoya A; Schroeder P; Mandla R; Deutsch AJ; Zhu W; Petty L; Yi X; Cole JB; Udler MS; Dornbos P; Porneala B; DiCorpo D; Liu CT; Li JH; Szczerbiński L; Kaur V; Kim J; Lu Y; Martin A; Eizirik DL; Marchetti P; Marselli L; Chen L; Srinivasan S; Todd J; Flannick J; Gubitosi-Klug R; Levitsky L; Shah R; Kelsey M; Burke B; Dabelea DM; Divers J; Marcovina S; Stalbow L; Loos RJF; Darst BF; Kooperberg C; Raffield LM; Haiman C; Sun Q; McCormick JB; Fisher-Hoch SP; Ordoñez ML; Meigs J; Baier LJ; González-Villalpando C; González-Villalpando ME; Orozco L; García-García L; Moreno-Estrada A; ; Aguilar-Salinas CA; Tusié T; Dupuis J; Ng MCY; Manning A; Highland HM; Cnop M; Hanson R; Below J; Florez JC; Leong A; Mercader JM
    Diabetologia; 2023 Jul; 66(7):1273-1288. PubMed ID: 37148359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.
    Liang J; Wang H; Cade BE; Kurniansyah N; He KY; Lee J; Sands SA; A Brody J; Chen H; Gottlieb DJ; Evans DS; Guo X; Gharib SA; Hale L; Hillman DR; Lutsey PL; Mukherjee S; Ochs-Balcom HM; Palmer LJ; Purcell S; Saxena R; Patel SR; Stone KL; Tranah GJ; Boerwinkle E; Lin X; Liu Y; Psaty BM; Vasan RS; Manichaikul A; Rich SS; Rotter JI; Sofer T; Redline S; Zhu X;
    Am J Respir Crit Care Med; 2022 Nov; 206(10):1271-1280. PubMed ID: 35822943
    [No Abstract]   [Full Text] [Related]  

  • 12. Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
    Liang J; Cade BE; He KY; Wang H; Lee J; Sofer T; Williams S; Li R; Chen H; Gottlieb DJ; Evans DS; Guo X; Gharib SA; Hale L; Hillman DR; Lutsey PL; Mukherjee S; Ochs-Balcom HM; Palmer LJ; Rhodes J; Purcell S; Patel SR; Saxena R; Stone KL; Tang W; Tranah GJ; Boerwinkle E; Lin X; Liu Y; Psaty BM; Vasan RS; Cho MH; Manichaikul A; Silverman EK; Barr RG; Rich SS; Rotter JI; Wilson JG; ; ; Redline S; Zhu X
    Am J Hum Genet; 2019 Nov; 105(5):1057-1068. PubMed ID: 31668705
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
    Wang Y; Selvaraj MS; Li X; Li Z; Holdcraft JA; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Cade BE; Carlson JC; Carson AP; Chen YI; Curran JE; de Vries PS; Dutcher SK; Ellinor PT; Floyd JS; Fornage M; Freedman BI; Gabriel S; Germer S; Gibbs RA; Guo X; He J; Heard-Costa N; Hildalgo B; Hou L; Irvin MR; Joehanes R; Kaplan RC; Kardia SL; Kelly TN; Kim R; Kooperberg C; Kral BG; Levy D; Li C; Liu C; Lloyd-Jone D; Loos RJ; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Murabito JM; Naseri T; O'Connell JR; Palmer ND; Preuss MH; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Ruepena MS; Sheu WH; Smith JA; Smith A; Tiwari HK; Tsai MY; Viaud-Martinez KA; Wang Z; Yanek LR; Zhao W; ; Rotter JI; Lin X; Natarajan P; Peloso GM
    Am J Hum Genet; 2023 Oct; 110(10):1704-1717. PubMed ID: 37802043
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.
    Sarnowski C; Chen H; Biggs ML; Wassertheil-Smoller S; Bressler J; Irvin MR; Ryan KA; Karasik D; Arnett DK; Cupples LA; Fardo DW; Gogarten SM; Heavner BD; Jain D; Kang HM; Kooperberg C; Mainous AG; Mitchell BD; Morrison AC; O'Connell JR; Psaty BM; Rice K; Smith AV; Vasan RS; Windham BG; Kiel DP; Murabito JM; Lunetta KL; ;
    PLoS One; 2021; 16(7):e0253611. PubMed ID: 34214102
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.
    Yu B; Pulit SL; Hwang SJ; Brody JA; Amin N; Auer PL; Bis JC; Boerwinkle E; Burke GL; Chakravarti A; Correa A; Dreisbach AW; Franco OH; Ehret GB; Franceschini N; Hofman A; Lin DY; Metcalf GA; Musani SK; Muzny D; Palmas W; Raffel L; Reiner A; Rice K; Rotter JI; Veeraraghavan N; Fox E; Guo X; North KE; Gibbs RA; van Duijn CM; Psaty BM; Levy D; Newton-Cheh C; Morrison AC;
    Circ Cardiovasc Genet; 2016 Feb; 9(1):64-70. PubMed ID: 26658788
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
    Mikhaylova AV; McHugh CP; Polfus LM; Raffield LM; Boorgula MP; Blackwell TW; Brody JA; Broome J; Chami N; Chen MH; Conomos MP; Cox C; Curran JE; Daya M; Ekunwe L; Glahn DC; Heard-Costa N; Highland HM; Hobbs BD; Ilboudo Y; Jain D; Lange LA; Miller-Fleming TW; Min N; Moon JY; Preuss MH; Rosen J; Ryan K; Smith AV; Sun Q; Surendran P; de Vries PS; Walter K; Wang Z; Wheeler M; Yanek LR; Zhong X; Abecasis GR; Almasy L; Barnes KC; Beaty TH; Becker LC; Blangero J; Boerwinkle E; Butterworth AS; Chavan S; Cho MH; Choquet H; Correa A; Cox N; DeMeo DL; Faraday N; Fornage M; Gerszten RE; Hou L; Johnson AD; Jorgenson E; Kaplan R; Kooperberg C; Kundu K; Laurie CA; Lettre G; Lewis JP; Li B; Li Y; Lloyd-Jones DM; Loos RJF; Manichaikul A; Meyers DA; Mitchell BD; Morrison AC; Ngo D; Nickerson DA; Nongmaithem S; North KE; O'Connell JR; Ortega VE; Pankratz N; Perry JA; Psaty BM; Rich SS; Soranzo N; Rotter JI; Silverman EK; Smith NL; Tang H; Tracy RP; Thornton TA; Vasan RS; Zein J; Mathias RA; ; Reiner AP; Auer PL
    Am J Hum Genet; 2021 Oct; 108(10):1836-1851. PubMed ID: 34582791
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder.
    Cruceanu C; Ambalavanan A; Spiegelman D; Gauthier J; Lafrenière RG; Dion PA; Alda M; Turecki G; Rouleau GA
    Genome; 2013 Oct; 56(10):634-40. PubMed ID: 24237345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
    Little A; Hu Y; Sun Q; Jain D; Broome J; Chen MH; Thibord F; McHugh C; Surendran P; Blackwell TW; Brody JA; Bhan A; Chami N; de Vries PS; Ekunwe L; Heard-Costa N; Hobbs BD; Manichaikul A; Moon JY; Preuss MH; Ryan K; Wang Z; Wheeler M; Yanek LR; Abecasis GR; Almasy L; Beaty TH; Becker LC; Blangero J; Boerwinkle E; Butterworth AS; Choquet H; Correa A; Curran JE; Faraday N; Fornage M; Glahn DC; Hou L; Jorgenson E; Kooperberg C; Lewis JP; Lloyd-Jones DM; Loos RJF; Min YI; Mitchell BD; Morrison AC; Nickerson DA; North KE; O'Connell JR; Pankratz N; Psaty BM; Vasan RS; Rich SS; Rotter JI; Smith AV; Smith NL; Tang H; Tracy RP; Conomos MP; Laurie CA; Mathias RA; Li Y; Auer PL; ; Thornton T; Reiner AP; Johnson AD; Raffield LM
    Hum Mol Genet; 2022 Feb; 31(3):347-361. PubMed ID: 34553764
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.