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Page 1
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
Arrington CB, Bleyl SB, Matsunami N, Bowles NE, Leppert TI, Demarest BL, Osborne K, Yoder BA, Byrne JL, Schiffman JD, Null DM, DiGeronimo R, Rollins M, Faix R, Comstock J, Camp NJ, Leppert MF, Yost HJ, Brunelli L. Arrington CB, et al. Among authors: camp nj. Am J Med Genet A. 2012 Dec;158A(12):3137-47. doi: 10.1002/ajmg.a.35664. Epub 2012 Nov 19. Am J Med Genet A. 2012. PMID: 23165927 Free PMC article.
A candidate prostate cancer susceptibility gene at chromosome 17p.
Tavtigian SV, Simard J, Teng DH, Abtin V, Baumgard M, Beck A, Camp NJ, Carillo AR, Chen Y, Dayananth P, Desrochers M, Dumont M, Farnham JM, Frank D, Frye C, Ghaffari S, Gupte JS, Hu R, Iliev D, Janecki T, Kort EN, Laity KE, Leavitt A, Leblanc G, McArthur-Morrison J, Pederson A, Penn B, Peterson KT, Reid JE, Richards S, Schroeder M, Smith R, Snyder SC, Swedlund B, Swensen J, Thomas A, Tranchant M, Woodland AM, Labrie F, Skolnick MH, Neuhausen S, Rommens J, Cannon-Albright LA. Tavtigian SV, et al. Among authors: camp nj. Nat Genet. 2001 Feb;27(2):172-80. doi: 10.1038/84808. Nat Genet. 2001. PMID: 11175785
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. Camp NJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):85-93. doi: 10.1002/ajmg.b.30177. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15806581
Linkage analysis of Tourette syndrome in a large Utah pedigree.
Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM; Tourette Syndrome Association International Consortium for Genetics. Knight S, et al. Among authors: camp nj. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):656-662. doi: 10.1002/ajmg.b.31035. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19777563 Free PMC article.
Shared genomic segment analysis: the power to find rare disease variants.
Knight S, Abo RP, Abel HJ, Neklason DW, Tuohy TM, Burt RW, Thomas A, Camp NJ. Knight S, et al. Among authors: camp nj. Ann Hum Genet. 2012 Nov;76(6):500-9. doi: 10.1111/j.1469-1809.2012.00728.x. Epub 2012 Sep 19. Ann Hum Genet. 2012. PMID: 22989048 Free PMC article.
211 results