H Donis-Keller
Overview
Explore the profile of H Donis-Keller including associated specialties, affiliations and a list of published articles.
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115
Citations
3103
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Recent Articles
1.
Oriola J, Halperin I, Rivera-Fillat F, Donis-Keller H
J Endocrinol Invest
. 2002 Mar;
25(1):25-31.
PMID: 11883863
Medullary thyroid carcinoma (MTC) occurs both sporadically and in the autosomal dominantly inherited multiple endocrine neoplasia (MEN) type 2 syndromes. The distinction between both is important for future clinical management....
2.
Glass A, Donis-Keller H, Mies C, Russo J, Zehnbauer B, Taube S, et al.
Clin Cancer Res
. 2001 Jul;
7(7):1843-9.
PMID: 11448894
Investigators continue to search for reliable markers of prognosis of breast cancer. For many analyses, laboratory techniques permit the use of archival paraffin-embedded tissue collected years previously and readily linked...
3.
Ghiasvand N, Fleming T, Helms C, Avisa A, Donis-Keller H
Am J Med Genet
. 2000 May;
92(3):220-3.
PMID: 10817658
Autosomal recessive nonsyndromic congenital retinal nonattachment (NCRNA) comprises congenital insensitivity to light, massive retrolental mass, shallow anterior chamber, microphthalmia, and nystagmus in otherwise normal individuals. Polymerase chain reaction-based linkage analyses...
4.
Ghiasvand N, Kanis A, Helms C, Sheffield V, Stone E, Donis-Keller H
Am J Med Genet
. 1999 Dec;
90(2):165-8.
PMID: 10607958
Nonsyndromic congenital retinal nonattachment (NCRNA) comprises congenital insensitivity to light, massive retrolental mass, shallow anterior chamber, microphthalmia, and nystagmus. We searched for the location of the gene responsible for an...
5.
Doll J, Zhu X, Furman J, Kaleem Z, Torres C, Humphrey P, et al.
Am J Pathol
. 1999 Sep;
155(3):967-71.
PMID: 10487854
Atypical adenomatous hyperplasia (AAH) of the prostate, a small glandular proliferation, is a putative precursor lesion to prostate cancer, in particular to the subset of well-differentiated carcinomas that arise in...
6.
Wang J, Radford D, Holt M, Helms C, Goate A, Brandt W, et al.
Genomics
. 1999 Aug;
60(1):1-11.
PMID: 10458905
We report the construction of an approximately 1.7-Mb sequence-ready YAC/BAC clone contig of 8p22-p23. This chromosomal region has been associated with frequent loss of heterozygosity (LOH) in breast, ovarian, prostate,...
7.
Urban Z, Michels V, Thibodeau S, Donis-Keller H, Csiszar K, Boyd C
Hum Genet
. 1999 Apr;
104(2):135-42.
PMID: 10190324
We have screened the elastin gene for mutations responsible for supravalvular aortic stenosis (SVAS) in two large, independently collected families with isolated (nonsyndromic) SVAS. By single-strand conformation polymorphism and heteroduplex...
8.
Inoue H, Tanizawa Y, Wasson J, BEHN P, Kalidas K, Bernal-Mizrachi E, et al.
Nat Genet
. 1998 Oct;
20(2):143-8.
PMID: 9771706
Wolfram syndrome (WFS; OMIM 222300) is an autosomal recessive neurodegenerative disorder defined by young-onset non-immune insulin-dependent diabetes mellitus and progressive optic atrophy. Linkage to markers on chromosome 4p was confirmed...
9.
Iannotti C, Inoue H, Bernal E, Aoki M, Liu L, Donis-Keller H, et al.
Genomics
. 1998 Jan;
46(3):520-4.
PMID: 9441763
LMX1 is a LIM-homeodomain (LIM-HD)-containing protein expressed selectively in insulin-producing beta-cell lines, and it it has been shown to activate insulin gene transcription. The human LMX1 gene was mapped by...
10.
Morton S, Veile R, Helms C, Lee M, Kuo W, Gray J, et al.
Genomics
. 1998 Jan;
46(3):491-4.
PMID: 9441757
Twenty-one putative chromosome 7-derived expressed sequence tags (ESTs) identified 33 yeast artificial chromosomes (YACs) or P1 clones, which were then used as reagents for physical mapping. FISH mapping established that...