187 related articles for article (PubMed ID: 31826912)
1. Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
Musolf AM; Moiz BA; Sun H; Pikielny CW; Bossé Y; Mandal D; de Andrade M; Gaba C; Yang P; Li Y; You M; Govindan R; Wilson RK; Kupert EY; Anderson MW; Schwartz AG; Pinney SM; Amos CI; Bailey-Wilson JE
Cancer Epidemiol Biomarkers Prev; 2020 Feb; 29(2):434-442. PubMed ID: 31826912
[TBL] [Abstract][Full Text] [Related]
2. Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study.
Wojciechowski R; Stambolian D; Ciner E; Ibay G; Holmes TN; Bailey-Wilson JE
Invest Ophthalmol Vis Sci; 2009 May; 50(5):2024-32. PubMed ID: 19151385
[TBL] [Abstract][Full Text] [Related]
3. Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q.
Fang S; Pinney SM; Bailey-Wilson JE; de Andrade MA; Li Y; Kupert E; You M; Schwartz AG; Yang P; Anderson MW; Amos CI
Cancer Epidemiol Biomarkers Prev; 2010 Dec; 19(12):3157-66. PubMed ID: 21030603
[TBL] [Abstract][Full Text] [Related]
4. Autosomal linkage analysis of a Japanese single multiplex schizophrenia pedigree reveals two candidate loci on chromosomes 4q and 3q.
Kaneko N; Muratake T; Kuwabara H; Kurosaki T; Takei M; Ohtsuki T; Arinami T; Tsuji S; Someya T
Am J Med Genet B Neuropsychiatr Genet; 2007 Sep; 144B(6):735-42. PubMed ID: 17671967
[TBL] [Abstract][Full Text] [Related]
5. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
Simpson CL; Musolf AM; Li Q; Portas L; Murgia F; Cordero RY; Cordero JB; Moiz BA; Holzinger ER; Middlebrooks CD; Lewis DD; Bailey-Wilson JE; Stambolian D
BMC Med Genet; 2019 Jan; 20(1):27. PubMed ID: 30704416
[TBL] [Abstract][Full Text] [Related]
6. Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.
Musolf AM; Simpson CL; Moiz BA; Pikielny CW; Middlebrooks CD; Mandal D; de Andrade M; Cole MD; Gaba C; Yang P; You M; Li Y; Kupert EY; Anderson MW; Schwartz AG; Pinney SM; Amos CI; Bailey-Wilson JE
Cancer Res; 2021 Jun; 81(12):3162-3173. PubMed ID: 33853833
[TBL] [Abstract][Full Text] [Related]
7. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area.
Shih WL; Yu MW; Chen PJ; Yeh SH; Lo MT; Chang HC; Liaw YF; Lin SM; Liu CJ; Lee SD; Lin CL; Hsiao CK; Yang SY; Chen CJ
Oncogene; 2006 May; 25(22):3219-24. PubMed ID: 16407824
[TBL] [Abstract][Full Text] [Related]
8. Multivariate analysis of anxiety disorders yields further evidence of linkage to chromosomes 4q21 and 7p in panic disorder families.
Logue MW; Bauver SR; Knowles JA; Gameroff MJ; Weissman MM; Crowe RR; Fyer AJ; Hamilton SP
Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):274-80. PubMed ID: 22253211
[TBL] [Abstract][Full Text] [Related]
9. Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.
Musolf AM; Simpson CL; Moiz BA; Long KA; Portas L; Murgia F; Ciner EB; Stambolian D; Bailey-Wilson JE
Invest Ophthalmol Vis Sci; 2017 Jul; 58(9):3547-3554. PubMed ID: 28715588
[TBL] [Abstract][Full Text] [Related]
10. Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Musolf AM; Ho WSC; Long KA; Zhuang Z; Argersinger DP; Sun H; Moiz BA; Simpson CL; Mendelevich EG; Bogdanov EI; Bailey-Wilson JE; Heiss JD
Eur J Hum Genet; 2019 Oct; 27(10):1599-1610. PubMed ID: 31227808
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.
Musolf AM; Simpson CL; Alexander TA; Portas L; Murgia F; Ciner EB; Stambolian D; Bailey-Wilson JE
Hum Genet; 2019 Apr; 138(4):339-354. PubMed ID: 30826882
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group.
Malhotra A; Igo RP; Thameem F; Kao WH; Abboud HE; Adler SG; Arar NH; Bowden DW; Duggirala R; Freedman BI; Goddard KA; Ipp E; Iyengar SK; Kimmel PL; Knowler WC; Kohn O; Leehey D; Meoni LA; Nelson RG; Nicholas SB; Parekh RS; Rich SS; Chen YD; Saad MF; Scavini M; Schelling JR; Sedor JR; Shah VO; Taylor KD; Thornley-Brown D; Zager PG; Horvath A; Hanson RL;
Diabetes Metab Res Rev; 2009 Nov; 25(8):740-7. PubMed ID: 19795399
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
Arason A; Gunnarsson H; Johannesdottir G; Jonasson K; Bendahl PO; Gillanders EM; Agnarsson BA; Jönsson G; Pylkäs K; Mustonen A; Heikkinen T; Aittomäki K; Blomqvist C; Melin B; Johannsson OT; Møller P; Winqvist R; Nevanlinna H; Borg A; Barkardottir RB
Breast Cancer Res; 2010; 12(4):R50. PubMed ID: 20637093
[TBL] [Abstract][Full Text] [Related]
14. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide scan for hypertension linkage to chromosome 12q23.1 - q23.3 in a Chinese family.
Dong Y; Yang L; Fang F; Zhang J; Jiang G; Xu S
Indian J Med Res; 2013 May; 137(5):935-41. PubMed ID: 23760380
[TBL] [Abstract][Full Text] [Related]
16. Identification of novel suggestive loci for high-grade myopia in Polish families.
Rydzanicz M; Nath SK; Sun C; Podfigurna-Musielak M; Frajdenberg A; Mrugacz M; Winters D; Ratnamala U; Radhakrishna U; Bejjani BA; Gajecka M
Mol Vis; 2011; 17():2028-39. PubMed ID: 21850178
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide scan of bipolar disorder and investigation of population stratification effects on linkage: support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13.
Cassidy F; Zhao C; Badger J; Claffey E; Dobrin S; Roche S; McKeon P
Am J Med Genet B Neuropsychiatr Genet; 2007 Sep; 144B(6):791-801. PubMed ID: 17455214
[TBL] [Abstract][Full Text] [Related]
18. A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
Grimm T; Garshasbi M; Puettmann L; Chen W; Ullmann R; Müller-Myhsok B; Klopocki E; Herbst L; Haug J; Jensen LR; Fischer C; Nöthen M; Ludwig K; Warnke A; Ott J; Schulte-Körne G; Ropers HH; Kuss AW
Z Kinder Jugendpsychiatr Psychother; 2020 Nov; 48(6):478-489. PubMed ID: 33172359
[No Abstract] [Full Text] [Related]
19. Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.
Camp NJ; Lowry MR; Richards RL; Plenk AM; Carter C; Hensel CH; Abkevich V; Skolnick MH; Shattuck D; Rowe KG; Hughes DC; Cannon-Albright LA
Am J Med Genet B Neuropsychiatr Genet; 2005 May; 135B(1):85-93. PubMed ID: 15806581
[TBL] [Abstract][Full Text] [Related]
20. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.
Toma C; Díaz-Gay M; Franch-Expósito S; Arnau-Collell C; Overs B; Muñoz J; Bonjoch L; Soares de Lima Y; Ocaña T; Cuatrecasas M; Castells A; Bujanda L; Balaguer F; Cubiella J; Caldés T; Fullerton JM; Castellví-Bel S
Int J Cancer; 2020 Mar; 146(6):1568-1577. PubMed ID: 31525256
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
