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Items: 1 to 20 of 175

1.

Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

Holberg CJ, Erickson RP, Bernas MJ, Witte MH, Fultz KE, Andrade M, Witte CL.

Am J Med Genet. 2001 Feb 1;98(4):303-12.

PMID:
11170072
2.

Linkage genome scan for loci predisposing to panic disorder or agoraphobia.

Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.

Am J Med Genet. 2001 Aug 8;105(6):548-57.

PMID:
11496373
3.

Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.

Malik S, Grzeschik KH.

Hum Genet. 2008 Mar;123(2):197-205. doi: 10.1007/s00439-007-0458-4. Epub 2008 Jan 10.

PMID:
18193458
4.

Genome-wide linkage analysis for celiac disease in North American families.

Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ.

Am J Med Genet. 2002 Jul 22;111(1):1-9.

PMID:
12124726
5.

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14.

Guo D, Hasham S, Kuang SQ, Vaughan CJ, Boerwinkle E, Chen H, Abuelo D, Dietz HC, Basson CT, Shete SS, Milewicz DM.

Circulation. 2001 May 22;103(20):2461-8.

6.

Genome wide scan using homozygosity mapping and linkage analyses of a single pedigree with affective disorder suggests oligogenic inheritance.

Ewald H, Kruse TA, Mors O.

Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):63-71.

PMID:
12815742
7.

Mapping of primary congenital lymphedema to the 5q35.3 region.

Evans AL, Brice G, Sotirova V, Mortimer P, Beninson J, Burnand K, Rosbotham J, Child A, Sarfarazi M.

Am J Hum Genet. 1999 Feb;64(2):547-55.

8.

Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

Ferrell RE, Levinson KL, Esman JH, Kimak MA, Lawrence EC, Barmada MM, Finegold DN.

Hum Mol Genet. 1998 Dec;7(13):2073-8.

9.

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. doi: 10.1016/j.ajhg.2009.03.005. Epub 2009 Mar 26.

10.

An autosomal genome-wide screen for celiac disease in Bedouin families.

Ding YC, Weizman Z, Yerushalmi B, Elbedour K, Garner CP, Neuhausen SL.

Genes Immun. 2008 Jan;9(1):81-6. Epub 2007 Oct 18.

PMID:
17943142
11.

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.

Hum Mol Genet. 2001 Nov 15;10(24):2751-65.

12.

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. Epub 2006 Dec 19.

PMID:
17179998
13.

Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.

Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.

Arch Neurol. 2006 Nov;63(11):1591-8.

PMID:
17101828
14.

Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4.

Goddard KA, Witte JS, Suarez BK, Catalona WJ, Olson JM.

Am J Hum Genet. 2001 May;68(5):1197-206. Epub 2001 Apr 13.

15.

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.

Hocking LJ, Herbert CA, Nicholls RK, Williams F, Bennett ST, Cundy T, Nicholson GC, Wuyts W, Van Hul W, Ralston SH.

Am J Hum Genet. 2001 Nov;69(5):1055-61. Epub 2001 Sep 5.

16.

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.

Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.

Mov Disord. 2006 Jan;21(1):28-33.

PMID:
16124010
17.

Genetic analysis of familial connective tissue alterations associated with cervical artery dissections suggests locus heterogeneity.

Wiest T, Hyrenbach S, Bambul P, Erker B, Pezzini A, Hausser I, Arnold ML, Martin JJ, Engelter S, Lyrer P, Busse O, Brandt T, Grond-Ginsbach C.

Stroke. 2006 Jul;37(7):1697-702. Epub 2006 May 25.

18.

Expanded genome scan in extended families with age-related macular degeneration.

Barral S, Francis PJ, Schultz DW, Schain MB, Haynes C, Majewski J, Ott J, Acott T, Weleber RG, Klein ML.

Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5453-9.

PMID:
17122136
19.

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.

PMID:
15656797
20.

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. Epub 2002 Feb 8.

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