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 *

236 related articles for article (PubMed ID: 28963451)

  • 1. CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
    Macé A; Tuke MA; Deelen P; Kristiansson K; Mattsson H; Nõukas M; Sapkota Y; Schick U; Porcu E; Rüeger S; McDaid AF; Porteous D; Winkler TW; Salvi E; Shrine N; Liu X; Ang WQ; Zhang W; Feitosa MF; Venturini C; van der Most PJ; Rosengren A; Wood AR; Beaumont RN; Jones SE; Ruth KS; Yaghootkar H; Tyrrell J; Havulinna AS; Boers H; Mägi R; Kriebel J; Müller-Nurasyid M; Perola M; Nieminen M; Lokki ML; Kähönen M; Viikari JS; Geller F; Lahti J; Palotie A; Koponen P; Lundqvist A; Rissanen H; Bottinger EP; Afaq S; Wojczynski MK; Lenzini P; Nolte IM; Sparsø T; Schupf N; Christensen K; Perls TT; Newman AB; Werge T; Snieder H; Spector TD; Chambers JC; Koskinen S; Melbye M; Raitakari OT; Lehtimäki T; Tobin MD; Wain LV; Sinisalo J; Peters A; Meitinger T; Martin NG; Wray NR; Montgomery GW; Medland SE; Swertz MA; Vartiainen E; Borodulin K; Männistö S; Murray A; Bochud M; Jacquemont S; Rivadeneira F; Hansen TF; Oldehinkel AJ; Mangino M; Province MA; Deloukas P; Kooner JS; Freathy RM; Pennell C; Feenstra B; Strachan DP; Lettre G; Hirschhorn J; Cusi D; Heid IM; Hayward C; Männik K; Beckmann JS; Loos RJF; Nyholt DR; Metspalu A; Eriksson JG; Weedon MN; Salomaa V; Franke L; Reymond A; Frayling TM; Kutalik Z
    Nat Commun; 2017 Sep; 8(1):744. PubMed ID: 28963451
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.
    Owen D; Bracher-Smith M; Kendall KM; Rees E; Einon M; Escott-Price V; Owen MJ; O'Donovan MC; Kirov G
    BMC Genomics; 2018 Dec; 19(1):867. PubMed ID: 30509170
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
    Berndt SI; Gustafsson S; Mägi R; Ganna A; Wheeler E; Feitosa MF; Justice AE; Monda KL; Croteau-Chonka DC; Day FR; Esko T; Fall T; Ferreira T; Gentilini D; Jackson AU; Luan J; Randall JC; Vedantam S; Willer CJ; Winkler TW; Wood AR; Workalemahu T; Hu YJ; Lee SH; Liang L; Lin DY; Min JL; Neale BM; Thorleifsson G; Yang J; Albrecht E; Amin N; Bragg-Gresham JL; Cadby G; den Heijer M; Eklund N; Fischer K; Goel A; Hottenga JJ; Huffman JE; Jarick I; Johansson Å; Johnson T; Kanoni S; Kleber ME; König IR; Kristiansson K; Kutalik Z; Lamina C; Lecoeur C; Li G; Mangino M; McArdle WL; Medina-Gomez C; Müller-Nurasyid M; Ngwa JS; Nolte IM; Paternoster L; Pechlivanis S; Perola M; Peters MJ; Preuss M; Rose LM; Shi J; Shungin D; Smith AV; Strawbridge RJ; Surakka I; Teumer A; Trip MD; Tyrer J; Van Vliet-Ostaptchouk JV; Vandenput L; Waite LL; Zhao JH; Absher D; Asselbergs FW; Atalay M; Attwood AP; Balmforth AJ; Basart H; Beilby J; Bonnycastle LL; Brambilla P; Bruinenberg M; Campbell H; Chasman DI; Chines PS; Collins FS; Connell JM; Cookson WO; de Faire U; de Vegt F; Dei M; Dimitriou M; Edkins S; Estrada K; Evans DM; Farrall M; Ferrario MM; Ferrières J; Franke L; Frau F; Gejman PV; Grallert H; Grönberg H; Gudnason V; Hall AS; Hall P; Hartikainen AL; Hayward C; Heard-Costa NL; Heath AC; Hebebrand J; Homuth G; Hu FB; Hunt SE; Hyppönen E; Iribarren C; Jacobs KB; Jansson JO; Jula A; Kähönen M; Kathiresan S; Kee F; Khaw KT; Kivimäki M; Koenig W; Kraja AT; Kumari M; Kuulasmaa K; Kuusisto J; Laitinen JH; Lakka TA; Langenberg C; Launer LJ; Lind L; Lindström J; Liu J; Liuzzi A; Lokki ML; Lorentzon M; Madden PA; Magnusson PK; Manunta P; Marek D; März W; Mateo Leach I; McKnight B; Medland SE; Mihailov E; Milani L; Montgomery GW; Mooser V; Mühleisen TW; Munroe PB; Musk AW; Narisu N; Navis G; Nicholson G; Nohr EA; Ong KK; Oostra BA; Palmer CN; Palotie A; Peden JF; Pedersen N; Peters A; Polasek O; Pouta A; Pramstaller PP; Prokopenko I; Pütter C; Radhakrishnan A; Raitakari O; Rendon A; Rivadeneira F; Rudan I; Saaristo TE; Sambrook JG; Sanders AR; Sanna S; Saramies J; Schipf S; Schreiber S; Schunkert H; Shin SY; Signorini S; Sinisalo J; Skrobek B; Soranzo N; Stančáková A; Stark K; Stephens JC; Stirrups K; Stolk RP; Stumvoll M; Swift AJ; Theodoraki EV; Thorand B; Tregouet DA; Tremoli E; Van der Klauw MM; van Meurs JB; Vermeulen SH; Viikari J; Virtamo J; Vitart V; Waeber G; Wang Z; Widén E; Wild SH; Willemsen G; Winkelmann BR; Witteman JC; Wolffenbuttel BH; Wong A; Wright AF; Zillikens MC; Amouyel P; Boehm BO; Boerwinkle E; Boomsma DI; Caulfield MJ; Chanock SJ; Cupples LA; Cusi D; Dedoussis GV; Erdmann J; Eriksson JG; Franks PW; Froguel P; Gieger C; Gyllensten U; Hamsten A; Harris TB; Hengstenberg C; Hicks AA; Hingorani A; Hinney A; Hofman A; Hovingh KG; Hveem K; Illig T; Jarvelin MR; Jöckel KH; Keinanen-Kiukaanniemi SM; Kiemeney LA; Kuh D; Laakso M; Lehtimäki T; Levinson DF; Martin NG; Metspalu A; Morris AD; Nieminen MS; Njølstad I; Ohlsson C; Oldehinkel AJ; Ouwehand WH; Palmer LJ; Penninx B; Power C; Province MA; Psaty BM; Qi L; Rauramaa R; Ridker PM; Ripatti S; Salomaa V; Samani NJ; Snieder H; Sørensen TI; Spector TD; Stefansson K; Tönjes A; Tuomilehto J; Uitterlinden AG; Uusitupa M; van der Harst P; Vollenweider P; Wallaschofski H; Wareham NJ; Watkins H; Wichmann HE; Wilson JF; Abecasis GR; Assimes TL; Barroso I; Boehnke M; Borecki IB; Deloukas P; Fox CS; Frayling T; Groop LC; Haritunian T; Heid IM; Hunter D; Kaplan RC; Karpe F; Moffatt MF; Mohlke KL; O'Connell JR; Pawitan Y; Schadt EE; Schlessinger D; Steinthorsdottir V; Strachan DP; Thorsteinsdottir U; van Duijn CM; Visscher PM; Di Blasio AM; Hirschhorn JN; Lindgren CM; Morris AP; Meyre D; Scherag A; McCarthy MI; Speliotes EK; North KE; Loos RJ; Ingelsson E
    Nat Genet; 2013 May; 45(5):501-12. PubMed ID: 23563607
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
    Vysotskiy M; Zhong X; Miller-Fleming TW; Zhou D; ; ; ; Cox NJ; Weiss LA
    Genome Med; 2021 Oct; 13(1):172. PubMed ID: 34715901
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
    Szatkiewicz JP; Neale BM; O'Dushlaine C; Fromer M; Goldstein JI; Moran JL; Chambert K; Kähler A; Magnusson PK; Hultman CM; Sklar P; Purcell S; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2013 Nov; 18(11):1178-84. PubMed ID: 23938935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci.
    Kettunen J; Perola M; Martin NG; Cornes BK; Wilson SG; Montgomery GW; Benyamin B; Harris JR; Boomsma D; Willemsen G; Hottenga JJ; Slagboom PE; Christensen K; Kyvik KO; Sørensen TI; Pedersen NL; Magnusson PK; Andrew T; Spector TD; Widen E; Silventoinen K; Kaprio J; Palotie A; Peltonen L;
    Int J Obes (Lond); 2009 Nov; 33(11):1235-42. PubMed ID: 19721450
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide association of anthropometric traits in African- and African-derived populations.
    Kang SJ; Chiang CW; Palmer CD; Tayo BO; Lettre G; Butler JL; Hackett R; Adeyemo AA; Guiducci C; Berzins I; Nguyen TT; Feng T; Luke A; Shriner D; Ardlie K; Rotimi C; Wilks R; Forrester T; McKenzie CA; Lyon HN; Cooper RS; Zhu X; Hirschhorn JN
    Hum Mol Genet; 2010 Jul; 19(13):2725-38. PubMed ID: 20400458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.
    Ulloa AE; Chen J; Vergara VM; Calhoun V; Liu J
    Alcohol Clin Exp Res; 2014 May; 38(5):1266-74. PubMed ID: 24512105
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
    Sanders SJ; Ercan-Sencicek AG; Hus V; Luo R; Murtha MT; Moreno-De-Luca D; Chu SH; Moreau MP; Gupta AR; Thomson SA; Mason CE; Bilguvar K; Celestino-Soper PB; Choi M; Crawford EL; Davis L; Wright NR; Dhodapkar RM; DiCola M; DiLullo NM; Fernandez TV; Fielding-Singh V; Fishman DO; Frahm S; Garagaloyan R; Goh GS; Kammela S; Klei L; Lowe JK; Lund SC; McGrew AD; Meyer KA; Moffat WJ; Murdoch JD; O'Roak BJ; Ober GT; Pottenger RS; Raubeson MJ; Song Y; Wang Q; Yaspan BL; Yu TW; Yurkiewicz IR; Beaudet AL; Cantor RM; Curland M; Grice DE; Günel M; Lifton RP; Mane SM; Martin DM; Shaw CA; Sheldon M; Tischfield JA; Walsh CA; Morrow EM; Ledbetter DH; Fombonne E; Lord C; Martin CL; Brooks AI; Sutcliffe JS; Cook EH; Geschwind D; Roeder K; Devlin B; State MW
    Neuron; 2011 Jun; 70(5):863-85. PubMed ID: 21658581
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways.
    Pettersson M; Viljakainen H; Loid P; Mustila T; Pekkinen M; Armenio M; Andersson-Assarsson JC; Mäkitie O; Lindstrand A
    J Clin Endocrinol Metab; 2017 Aug; 102(8):3029-3039. PubMed ID: 28605459
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
    Speliotes EK; Willer CJ; Berndt SI; Monda KL; Thorleifsson G; Jackson AU; Lango Allen H; Lindgren CM; Luan J; Mägi R; Randall JC; Vedantam S; Winkler TW; Qi L; Workalemahu T; Heid IM; Steinthorsdottir V; Stringham HM; Weedon MN; Wheeler E; Wood AR; Ferreira T; Weyant RJ; Segrè AV; Estrada K; Liang L; Nemesh J; Park JH; Gustafsson S; Kilpeläinen TO; Yang J; Bouatia-Naji N; Esko T; Feitosa MF; Kutalik Z; Mangino M; Raychaudhuri S; Scherag A; Smith AV; Welch R; Zhao JH; Aben KK; Absher DM; Amin N; Dixon AL; Fisher E; Glazer NL; Goddard ME; Heard-Costa NL; Hoesel V; Hottenga JJ; Johansson A; Johnson T; Ketkar S; Lamina C; Li S; Moffatt MF; Myers RH; Narisu N; Perry JR; Peters MJ; Preuss M; Ripatti S; Rivadeneira F; Sandholt C; Scott LJ; Timpson NJ; Tyrer JP; van Wingerden S; Watanabe RM; White CC; Wiklund F; Barlassina C; Chasman DI; Cooper MN; Jansson JO; Lawrence RW; Pellikka N; Prokopenko I; Shi J; Thiering E; Alavere H; Alibrandi MT; Almgren P; Arnold AM; Aspelund T; Atwood LD; Balkau B; Balmforth AJ; Bennett AJ; Ben-Shlomo Y; Bergman RN; Bergmann S; Biebermann H; Blakemore AI; Boes T; Bonnycastle LL; Bornstein SR; Brown MJ; Buchanan TA; Busonero F; Campbell H; Cappuccio FP; Cavalcanti-Proença C; Chen YD; Chen CM; Chines PS; Clarke R; Coin L; Connell J; Day IN; den Heijer M; Duan J; Ebrahim S; Elliott P; Elosua R; Eiriksdottir G; Erdos MR; Eriksson JG; Facheris MF; Felix SB; Fischer-Posovszky P; Folsom AR; Friedrich N; Freimer NB; Fu M; Gaget S; Gejman PV; Geus EJ; Gieger C; Gjesing AP; Goel A; Goyette P; Grallert H; Grässler J; Greenawalt DM; Groves CJ; Gudnason V; Guiducci C; Hartikainen AL; Hassanali N; Hall AS; Havulinna AS; Hayward C; Heath AC; Hengstenberg C; Hicks AA; Hinney A; Hofman A; Homuth G; Hui J; Igl W; Iribarren C; Isomaa B; Jacobs KB; Jarick I; Jewell E; John U; Jørgensen T; Jousilahti P; Jula A; Kaakinen M; Kajantie E; Kaplan LM; Kathiresan S; Kettunen J; Kinnunen L; Knowles JW; Kolcic I; König IR; Koskinen S; Kovacs P; Kuusisto J; Kraft P; Kvaløy K; Laitinen J; Lantieri O; Lanzani C; Launer LJ; Lecoeur C; Lehtimäki T; Lettre G; Liu J; Lokki ML; Lorentzon M; Luben RN; Ludwig B; ; Manunta P; Marek D; Marre M; Martin NG; McArdle WL; McCarthy A; McKnight B; Meitinger T; Melander O; Meyre D; Midthjell K; Montgomery GW; Morken MA; Morris AP; Mulic R; Ngwa JS; Nelis M; Neville MJ; Nyholt DR; O'Donnell CJ; O'Rahilly S; Ong KK; Oostra B; Paré G; Parker AN; Perola M; Pichler I; Pietiläinen KH; Platou CG; Polasek O; Pouta A; Rafelt S; Raitakari O; Rayner NW; Ridderstråle M; Rief W; Ruokonen A; Robertson NR; Rzehak P; Salomaa V; Sanders AR; Sandhu MS; Sanna S; Saramies J; Savolainen MJ; Scherag S; Schipf S; Schreiber S; Schunkert H; Silander K; Sinisalo J; Siscovick DS; Smit JH; Soranzo N; Sovio U; Stephens J; Surakka I; Swift AJ; Tammesoo ML; Tardif JC; Teder-Laving M; Teslovich TM; Thompson JR; Thomson B; Tönjes A; Tuomi T; van Meurs JB; van Ommen GJ; Vatin V; Viikari J; Visvikis-Siest S; Vitart V; Vogel CI; Voight BF; Waite LL; Wallaschofski H; Walters GB; Widen E; Wiegand S; Wild SH; Willemsen G; Witte DR; Witteman JC; Xu J; Zhang Q; Zgaga L; Ziegler A; Zitting P; Beilby JP; Farooqi IS; Hebebrand J; Huikuri HV; James AL; Kähönen M; Levinson DF; Macciardi F; Nieminen MS; Ohlsson C; Palmer LJ; Ridker PM; Stumvoll M; Beckmann JS; Boeing H; Boerwinkle E; Boomsma DI; Caulfield MJ; Chanock SJ; Collins FS; Cupples LA; Smith GD; Erdmann J; Froguel P; Grönberg H; Gyllensten U; Hall P; Hansen T; Harris TB; Hattersley AT; Hayes RB; Heinrich J; Hu FB; Hveem K; Illig T; Jarvelin MR; Kaprio J; Karpe F; Khaw KT; Kiemeney LA; Krude H; Laakso M; Lawlor DA; Metspalu A; Munroe PB; Ouwehand WH; Pedersen O; Penninx BW; Peters A; Pramstaller PP; Quertermous T; Reinehr T; Rissanen A; Rudan I; Samani NJ; Schwarz PE; Shuldiner AR; Spector TD; Tuomilehto J; Uda M; Uitterlinden A; Valle TT; Wabitsch M; Waeber G; Wareham NJ; Watkins H; ; Wilson JF; Wright AF; Zillikens MC; Chatterjee N; McCarroll SA; Purcell S; Schadt EE; Visscher PM; Assimes TL; Borecki IB; Deloukas P; Fox CS; Groop LC; Haritunians T; Hunter DJ; Kaplan RC; Mohlke KL; O'Connell JR; Peltonen L; Schlessinger D; Strachan DP; van Duijn CM; Wichmann HE; Frayling TM; Thorsteinsdottir U; Abecasis GR; Barroso I; Boehnke M; Stefansson K; North KE; McCarthy MI; Hirschhorn JN; Ingelsson E; Loos RJ
    Nat Genet; 2010 Nov; 42(11):937-48. PubMed ID: 20935630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.
    Yang TL; Guo Y; Li SM; Li SK; Tian Q; Liu YJ; Deng HW
    Int J Obes (Lond); 2013 Feb; 37(2):188-90. PubMed ID: 22391884
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The individual and global impact of copy-number variants on complex human traits.
    Auwerx C; Lepamets M; Sadler MC; Patxot M; Stojanov M; Baud D; Mägi R; ; Porcu E; Reymond A; Kutalik Z
    Am J Hum Genet; 2022 Apr; 109(4):647-668. PubMed ID: 35240056
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
    Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
    Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide analysis of copy number variations reveals that aging processes influence body fat distribution in Korea Associated Resource (KARE) cohorts.
    Lee BY; Shin DH; Cho S; Seo KS; Kim H
    Hum Genet; 2012 Nov; 131(11):1795-804. PubMed ID: 22825314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry.
    Yengo L; Sidorenko J; Kemper KE; Zheng Z; Wood AR; Weedon MN; Frayling TM; Hirschhorn J; Yang J; Visscher PM;
    Hum Mol Genet; 2018 Oct; 27(20):3641-3649. PubMed ID: 30124842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Age-stratified QTL genome scan analyses for anthropometric measures.
    Beck SR; Brown WM; Williams AH; Pierce J; Rich SS; Langefeld CD
    BMC Genet; 2003 Dec; 4 Suppl 1(Suppl 1):S31. PubMed ID: 14975099
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenome-wide Burden of Copy-Number Variation in the UK Biobank.
    Aguirre M; Rivas MA; Priest J
    Am J Hum Genet; 2019 Aug; 105(2):373-383. PubMed ID: 31353025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
    Randall JC; Winkler TW; Kutalik Z; Berndt SI; Jackson AU; Monda KL; Kilpeläinen TO; Esko T; Mägi R; Li S; Workalemahu T; Feitosa MF; Croteau-Chonka DC; Day FR; Fall T; Ferreira T; Gustafsson S; Locke AE; Mathieson I; Scherag A; Vedantam S; Wood AR; Liang L; Steinthorsdottir V; Thorleifsson G; Dermitzakis ET; Dimas AS; Karpe F; Min JL; Nicholson G; Clegg DJ; Person T; Krohn JP; Bauer S; Buechler C; Eisinger K; ; Bonnefond A; Froguel P; ; Hottenga JJ; Prokopenko I; Waite LL; Harris TB; Smith AV; Shuldiner AR; McArdle WL; Caulfield MJ; Munroe PB; Grönberg H; Chen YD; Li G; Beckmann JS; Johnson T; Thorsteinsdottir U; Teder-Laving M; Khaw KT; Wareham NJ; Zhao JH; Amin N; Oostra BA; Kraja AT; Province MA; Cupples LA; Heard-Costa NL; Kaprio J; Ripatti S; Surakka I; Collins FS; Saramies J; Tuomilehto J; Jula A; Salomaa V; Erdmann J; Hengstenberg C; Loley C; Schunkert H; Lamina C; Wichmann HE; Albrecht E; Gieger C; Hicks AA; Johansson A; Pramstaller PP; Kathiresan S; Speliotes EK; Penninx B; Hartikainen AL; Jarvelin MR; Gyllensten U; Boomsma DI; Campbell H; Wilson JF; Chanock SJ; Farrall M; Goel A; Medina-Gomez C; Rivadeneira F; Estrada K; Uitterlinden AG; Hofman A; Zillikens MC; den Heijer M; Kiemeney LA; Maschio A; Hall P; Tyrer J; Teumer A; Völzke H; Kovacs P; Tönjes A; Mangino M; Spector TD; Hayward C; Rudan I; Hall AS; Samani NJ; Attwood AP; Sambrook JG; Hung J; Palmer LJ; Lokki ML; Sinisalo J; Boucher G; Huikuri H; Lorentzon M; Ohlsson C; Eklund N; Eriksson JG; Barlassina C; Rivolta C; Nolte IM; Snieder H; Van der Klauw MM; Van Vliet-Ostaptchouk JV; Gejman PV; Shi J; Jacobs KB; Wang Z; Bakker SJ; Mateo Leach I; Navis G; van der Harst P; Martin NG; Medland SE; Montgomery GW; Yang J; Chasman DI; Ridker PM; Rose LM; Lehtimäki T; Raitakari O; Absher D; Iribarren C; Basart H; Hovingh KG; Hyppönen E; Power C; Anderson D; Beilby JP; Hui J; Jolley J; Sager H; Bornstein SR; Schwarz PE; Kristiansson K; Perola M; Lindström J; Swift AJ; Uusitupa M; Atalay M; Lakka TA; Rauramaa R; Bolton JL; Fowkes G; Fraser RM; Price JF; Fischer K; Krjutå Kov K; Metspalu A; Mihailov E; Langenberg C; Luan J; Ong KK; Chines PS; Keinanen-Kiukaanniemi SM; Saaristo TE; Edkins S; Franks PW; Hallmans G; Shungin D; Morris AD; Palmer CN; Erbel R; Moebus S; Nöthen MM; Pechlivanis S; Hveem K; Narisu N; Hamsten A; Humphries SE; Strawbridge RJ; Tremoli E; Grallert H; Thorand B; Illig T; Koenig W; Müller-Nurasyid M; Peters A; Boehm BO; Kleber ME; März W; Winkelmann BR; Kuusisto J; Laakso M; Arveiler D; Cesana G; Kuulasmaa K; Virtamo J; Yarnell JW; Kuh D; Wong A; Lind L; de Faire U; Gigante B; Magnusson PK; Pedersen NL; Dedoussis G; Dimitriou M; Kolovou G; Kanoni S; Stirrups K; Bonnycastle LL; Njølstad I; Wilsgaard T; Ganna A; Rehnberg E; Hingorani A; Kivimaki M; Kumari M; Assimes TL; Barroso I; Boehnke M; Borecki IB; Deloukas P; Fox CS; Frayling T; Groop LC; Haritunians T; Hunter D; Ingelsson E; Kaplan R; Mohlke KL; O'Connell JR; Schlessinger D; Strachan DP; Stefansson K; van Duijn CM; Abecasis GR; McCarthy MI; Hirschhorn JN; Qi L; Loos RJ; Lindgren CM; North KE; Heid IM
    PLoS Genet; 2013 Jun; 9(6):e1003500. PubMed ID: 23754948
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
    Levinson DF; Duan J; Oh S; Wang K; Sanders AR; Shi J; Zhang N; Mowry BJ; Olincy A; Amin F; Cloninger CR; Silverman JM; Buccola NG; Byerley WF; Black DW; Kendler KS; Freedman R; Dudbridge F; Pe'er I; Hakonarson H; Bergen SE; Fanous AH; Holmans PA; Gejman PV
    Am J Psychiatry; 2011 Mar; 168(3):302-16. PubMed ID: 21285140
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.