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 *

132 related articles for article (PubMed ID: 23386034)

  • 1. A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18.
    Majander KK; Villa PM; Kivinen K; Kere J; Laivuori H
    Eur J Hum Genet; 2013 Sep; 21(9):1024-6. PubMed ID: 23386034
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PP009. A follow-up study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18.
    Laivuori HM; Majander KK; Villa P; Kivinen K; Kere J
    Pregnancy Hypertens; 2012 Jul; 2(3):244-5. PubMed ID: 26105332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.
    Laivuori H; Lahermo P; Ollikainen V; Widen E; Häivä-Mällinen L; Sundström H; Laitinen T; Kaaja R; Ylikorkala O; Kere J
    Am J Hum Genet; 2003 Jan; 72(1):168-77. PubMed ID: 12474145
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2.
    Moses EK; Lade JA; Guo G; Wilton AN; Grehan M; Freed K; Borg A; Terwilliger JD; North R; Cooper DW; Brennecke SP
    Am J Hum Genet; 2000 Dec; 67(6):1581-5. PubMed ID: 11035632
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2.
    Fitzpatrick E; Göring HH; Liu H; Borg A; Forrest S; Cooper DW; Brennecke SP; Moses EK
    Hum Biol; 2004 Dec; 76(6):849-62. PubMed ID: 15974297
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
    Lindgren CM; Mahtani MM; Widén E; McCarthy MI; Daly MJ; Kirby A; Reeve MP; Kruglyak L; Parker A; Meyer J; Almgren P; Lehto M; Kanninen T; Tuomi T; Groop LC; Lander ES
    Am J Hum Genet; 2002 Feb; 70(2):509-16. PubMed ID: 11791216
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.
    Arngrímsson R; Sigurõardóttir S; Frigge ML; Bjarnadóttir RI; Jónsson T; Stefánsson H; Baldursdóttir A; Einarsdóttir AS; Palsson B; Snorradóttir S; Lachmeijer AM; Nicolae D; Kong A; Bragason BT; Gulcher JR; Geirsson RT; Stefánsson K
    Hum Mol Genet; 1999 Sep; 8(9):1799-805. PubMed ID: 10441346
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis.
    Schwab SG; Hallmayer J; Lerer B; Albus M; Borrmann M; Hönig S; Strauss M; Segman R; Lichtermann D; Knapp M; Trixler M; Maier W; Wildenauer DB
    Am J Hum Genet; 1998 Oct; 63(4):1139-52. PubMed ID: 9758604
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A genome-wide scan for preeclampsia in the Netherlands.
    Lachmeijer AM; Arngrímsson R; Bastiaans EJ; Frigge ML; Pals G; Sigurdardóttir S; Stéfansson H; Pálsson B; Nicolae D; Kong A; Aarnoudse JG; Gulcher JR; Dekker GA; ten Kate LP; Stéfansson K
    Eur J Hum Genet; 2001 Oct; 9(10):758-64. PubMed ID: 11781687
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.
    Marcheco-Teruel B; Flint TJ; Wikman FP; Torralbas M; González L; Blanco L; Tan Q; Ewald H; Orntoft T; Kruse TA; Børglum AD; Mors O
    Am J Med Genet B Neuropsychiatr Genet; 2006 Dec; 141B(8):833-43. PubMed ID: 16917938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26.
    Schleutker J; Baffoe-Bonnie AB; Gillanders E; Kainu T; Jones MP; Freas-Lutz D; Markey C; Gildea D; Riedesel E; Albertus J; Gibbs KD; Matikainen M; Koivisto PA; Tammela T; Bailey-Wilson JE; Trent JM; Kallioniemi OP
    Prostate; 2003 Dec; 57(4):280-9. PubMed ID: 14601024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage and association mapping of a chromosome 1q21-q24 type 2 diabetes susceptibility locus in northern European Caucasians.
    Das SK; Hasstedt SJ; Zhang Z; Elbein SC
    Diabetes; 2004 Feb; 53(2):492-9. PubMed ID: 14747303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of two novel quantitative trait loci for pre-eclampsia susceptibility on chromosomes 5q and 13q using a variance components-based linkage approach.
    Johnson MP; Fitzpatrick E; Dyer TD; Jowett JB; Brennecke SP; Blangero J; Moses EK
    Mol Hum Reprod; 2007 Jan; 13(1):61-7. PubMed ID: 17085769
    [TBL] [Abstract][Full Text] [Related]  

  • 15. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
    Sander T; Windemuth C; Schulz H; Saar K; Gennaro E; Bianchi A; Zara F; Bulteau C; Kaminska A; Ville D; Cieuta C; Prud'homme JF; Dulac O; Bate L; Gardiner RM; de Haan GJ; Janssen GA; Witte J; Halley DJ; Lindhout D; Wienker TF; Janz D;
    Am J Med Genet; 2002 Aug; 114(6):673-8. PubMed ID: 12210286
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.
    Gao X; Martin ER; Liu Y; Mayhew G; Vance JM; Scott WK
    Am J Hum Genet; 2009 Apr; 84(4):499-504. PubMed ID: 19327735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A susceptibility locus for migraine with aura, on chromosome 4q24.
    Wessman M; Kallela M; Kaunisto MA; Marttila P; Sobel E; Hartiala J; Oswell G; Leal SM; Papp JC; Hämäläinen E; Broas P; Joslyn G; Hovatta I; Hiekkalinna T; Kaprio J; Ott J; Cantor RM; Zwart JA; Ilmavirta M; Havanka H; Färkkilä M; Peltonen L; Palotie A
    Am J Hum Genet; 2002 Mar; 70(3):652-62. PubMed ID: 11836652
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes.
    Wessman M; Forsblom C; Kaunisto MA; Söderlund J; Ilonen J; Sallinen R; Hiekkalinna T; Parkkonen M; Maxwell AP; Tarnow L; Parving HH; Hadjadj S; Marre M; Peltonen L; Groop PH;
    PLoS One; 2011; 6(9):e24053. PubMed ID: 21909410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.
    Moses EK; Fitzpatrick E; Freed KA; Dyer TD; Forrest S; Elliott K; Johnson MP; Blangero J; Brennecke SP
    Mol Hum Reprod; 2006 Aug; 12(8):505-12. PubMed ID: 16809377
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
    Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
    Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.