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Werner Syndrome
Known as:
syndromes werner's
, PROGERIA, OF ADULT
, Adult Progeria
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An inherited disorder marked by rapid aging that begins in early adolescence. Patients may be shorter than average, and have health problems such as…
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National Institutes of Health
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Related topics
Related topics
33 relations
Autosomal recessive inheritance
Cataract
Chromosomes, Human, Pair 8
Diabetes Mellitus
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Broader (3)
Hereditary Diseases
Premature aging syndrome
Syndrome
Narrower (2)
Lipomatosis, Multiple Symmetrical
Peptide growth factors deficiency
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
THE DIRECT COLLAPSE OF A MASSIVE BLACK HOLE SEED UNDER THE INFLUENCE OF AN ANISOTROPIC LYMAN–WERNER SOURCE
J. Regan
,
P. Johansson
,
J. Wise
2014
Corpus ID: 119119172
The direct collapse model of supermassive black hole seed formation requires that the gas cools predominantly via atomic hydrogen…
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2007
2007
An association of Hutchinson–Gilford progeria and malignancy
S. Shalev
,
Annachiara De Sandre-Giovannoli
,
A. Shani
,
N. Lévy
American Journal of Medical Genetics. Part A
2007
Corpus ID: 11588430
Mutations in the LMNA gene encoding lamins A/C are responsible for a variety of disorders, commonly referred to as “laminopathies…
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Highly Cited
2006
Highly Cited
2006
Quality of life and psychosocial situation before and after a lung, liver or an allogeneic bone marrow transplant.
L. Goetzmann
,
R. Klaghofer
,
+5 authors
C. Buddeberg
Swiss medical weekly
2006
Corpus ID: 21457503
BACKGROUND AND OBJECTIVES Only few comparative prospective studies have been published on psychosocial issues of organ transplant…
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2001
2001
HIRSCHBIEGEL, Jan, PARAVICINI, Werner, Das Frauenzimmer. Die Frau bei Hofe in Spätmittelalter und Früher Neuzeit
Naïma Ghermani
2001
Corpus ID: 193006266
Sans doute davantage qu’en France, le courant historiographique anglo-saxon des gender studies a trouve un grand echo parmi les…
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2000
2000
Spectral karyotyping of Werner syndrome fibroblast cultures
Ralph E. Melcher
,
R. V. Golitschek
,
+5 authors
H. Hoehn
Cytogenetic and Genome Research
2000
Corpus ID: 32955295
Fibroblast cultures from two Werner syndrome patients were analyzed by spectral karyotyping. There were multiple, pseudodiploid…
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1996
1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
K. Goddard
,
Chang-En Yu
,
+6 authors
E. Wijsman
American Journal of Human Genetics
1996
Corpus ID: 20787806
Werner syndrome (WS) is an autosomal recessive disorder characterized by premature onset of a number of age-related diseases. The…
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1992
1992
Der historische Horizont der Götterbild-Amulette aus der Übergangsepoche von der Spätantike zum Frühmittelalter : Bericht über das Colloquium vom 28. 11.-1. 12. 1988 in der Werner-Reimers-Stiftung…
Karl Hauck
1992
Corpus ID: 177309438
Highly Cited
1985
Highly Cited
1985
Cytogenetic aspects of Werner syndrome.
Darrell Salk
,
K. Au
,
Holger Hoehn
,
George M. Martin
Advances in Experimental Medicine and Biology
1985
Corpus ID: 39470819
Cultured skin fibroblast-like (FL) cells from patients with Werner syndrome display frequent pseudodiploidy involving multiple…
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Review
1982
Review
1982
Syndromes of accelerated aging.
G. Martin
National Cancer Institute monograph
1982
Corpus ID: 33555963
A systematic review of the more than 2,000 genetic loci of man cataloged by McKusick indicated that approximately 7% may play a…
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Highly Cited
1976
Highly Cited
1976
Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderrna pigmentosum
C. Bartram
,
T. Koske‐Westphal
,
E. Passarge
Annals of Human Genetics
1976
Corpus ID: 6938834
The frequency of BrdU-induced sister chromatid exchanges (SCE) in cultured lymphocytes from patients with ataxia telangiectasia…
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