Follow
Wolfram Henn
Wolfram Henn
Human Genetics and Medical Ethics, Saarland University
Verified email at uks.eu
Title
Cited by
Cited by
Year
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations
JJ Johnston, I Olivos-Glander, C Killoran, E Elson, JT Turner, KF Peters, ...
The American Journal of Human Genetics 76 (4), 609-622, 2005
3022005
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation
Ö Altug Teber, G Gillessen-Kaesbach, S Fischer, S Böhringer, B Albrecht, ...
European Journal of Human Genetics 12 (11), 879-890, 2004
2032004
Psychological benefit of diagnostic certainty for mothers of children with disabilities: lessons from Down syndrome
W Lenhard, E Breitenbach, H Ebert, HJ Schindelhauer‐Deutscher, ...
American Journal of Medical Genetics Part A 133 (2), 170-175, 2005
1642005
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements
H Starke, J Seidel, W Henn, S Reichardt, M Volleth, M Stumm, C Behrend, ...
European Journal of Human Genetics 10 (12), 790-800, 2002
1452002
Predictive value of progression-associated chromosomal aberrations for the prognosis of meningiomas: a retrospective study of 198 cases
R Ketter, W Henn, I Niedermayer, H Steilen-Gimbel, J König, KD Zang, ...
Journal of neurosurgery 95 (4), 601-607, 2001
1432001
Triple approach for diagnosis and grading of meningiomas: histology, morphometry of Ki-67/Feulgen stainings, and cytogenetics
H Kolles, I Niedermayer, CH Schmitt, W Henn, R Feld, WI Steudel, ...
Acta neurochirurgica 137, 174-181, 1995
1421995
Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy
JS Weiss, HS Kruth, H Kuivaniemi, G Tromp, PS White, RS Winters, ...
Investigative ophthalmology & visual science 48 (11), 5007-5012, 2007
1312007
Evidence of focal genetic microheterogeneity in glioblastoma multiforme by area-specific CGH on microdissected tumor cells
V Jung, BFM Romeike, W Henn, W Feiden, JR Moringlane, KD Zang, ...
Journal of neuropathology and experimental neurology 58 (9), 993-999, 1999
1271999
Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas
P Müller, W Henn, I Niedermayer, R Ketter, W Feiden, WI Steudel, ...
Clinical cancer research 5 (11), 3569-3577, 1999
1221999
Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants
C Pagenstecher, M Wehner, W Friedl, N Rahner, S Aretz, N Friedrichs, ...
Human genetics 119, 9-22, 2006
1012006
Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1
S Krüger, M Kinzel, C Walldorf, S Gottschling, A Bier, S Tinschert, ...
European Journal of Human Genetics 16 (1), 62-72, 2008
972008
Histopathologic indicators of recurrence in meningiomas: correlation with clinical and genetic parameters
YJ Kim, R Ketter, W Henn, KD Zang, WI Steudel, W Feiden
Virchows Archiv 449, 529-538, 2006
942006
Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines
W Henn, N Blin, KD Zang
Human genetics 74 (1), 104-106, 1986
891986
Loss of alkaline phosphatase activity in meningiomas: a rapid histochemical technique indicating progression-associated deletion of a putative tumor suppressor gene on the …
I Niedermayer, W Feiden, W Henn, H Steilen-Gimbel, WI Steudel, ...
Journal of Neuropathology & Experimental Neurology 56 (8), 879-886, 1997
831997
Telomeric associations and loss of telomeric DNA repeats in renal tumors
K Holzmann, N Blin, C Welter, KD Zang, G Seitz, W Henn
Genes, Chromosomes and Cancer 6 (3), 178-181, 1993
831993
Correspondence of tumor localization with tumor recurrence and cytogenetic progression in meningiomas
R Ketter, J Rahnenführer, W Henn, YJ Kim, W Feiden, WI Steudel, ...
Neurosurgery 62 (1), 61-70, 2008
792008
An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis
D Schmitz, C Netzer, W Henn
Nature Reviews Genetics 10 (8), 515-515, 2009
772009
Malignant odontogenic myxoma of the maxilla: case with cytogenetic confirmation
S Pahl, W Henn, T Binger, U Stein, K Remberger
The Journal of Laryngology & Otology 114 (7), 533-535, 2000
722000
High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one‐third of probands are minors
S Spiegler, J Najm, J Liu, S Gkalympoudis, W Schröder, G Borck, ...
Molecular genetics & genomic medicine 2 (2), 176-185, 2014
672014
Constitutive expression of c-fos and c-jun, overexpression of ets-2, and reduced expression of metastasis suppressor gene nm23-H1 in rheumatoid arthritis.
S Dooley, I Herlitzka, R Hanselmann, A Ermis, W Henn, K Remberger, ...
Annals of the rheumatic diseases 55 (5), 298-304, 1996
661996
The system can't perform the operation now. Try again later.
Articles 1–20