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Ilse Wieland

Mutations of the Ephrin-B1 Gene Cause Craniofrontonasal Syndrome
2004 · Ilse Wieland, Sibylle Jakubiczka, et al. · The American Journal of Human Genetics · 243
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Cloning and characterization of CAP, the S. cerevisiae gene encoding the 70 kd adenylyl cyclase-associated protein
1990 · J. Field, A. Vojtek, et al. · Cell · 243
A novel member of the NF2/ERM/4.1 superfamily with growth suppressing properties in lung cancer.
1999 · Y K Tran, O Bögler, et al. · PubMed · 147
Microbeam MOMeNT: non-contact laser microdissection of membrane-mounted native tissue.
1997 · M Böhm, I Wieland, et al. · Europe PMC (PubMed Central) · 114
A method for difference cloning: gene amplification following subtractive hybridization.
1990 · I Wieland, G Bolger, et al. · Proceedings of the National Academy of Sciences · 93
Differences of E-cadherin expression levels and patterns in primary and metastatic human lung cancer
1994 · Malte Böhm, Baldur Totzeck, et al. · Clinical & Experimental Metastasis · 77
Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis
2016 · S. Boppudi, N. Bögershausen, et al. · Clinical Genetics · 74
Clinical and genetic aspects of craniofrontonasal syndrome: Towards resolving a genetic paradox
2005 · Peter Wieacker, Ilse Wieland · Molecular Genetics and Metabolism · 69
Isolation of DICE1: A gene frequently affected by LOH and downregulated in lung carcinomas
1999 · I Wieland, K C Arden, et al. · Oncogene · 66
NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly
2018 · Ina Schanze, Jens Bunt, et al. · The American Journal of Human Genetics · 63
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Twenty-six novelEFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)
2005 · Ilse Wieland, William Reardon, et al. · Human Mutation · 63
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Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies
2019 · Oscar F. Chacon‐Camacho, Daniel Lopez‐Moreno, et al. · Molecular Genetics & Genomic Medicine · 59
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High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)
2006 · Ilse Wieland, Petra Muschke, et al. · Genes Chromosomes and Cancer · 49
Clinical and Genetic Evaluation of Patients with KATP Channel Mutations from the German Registry for Congenital Hyperinsulinism
2014 · Klaus Mohnike, Ilse Wieland, et al. · Hormone Research in Paediatrics · 45
Frequent allelic deletion at a novel locus on chromosome 5 in human lung cancer
1994 · I Wieland, M Böhm · Lung Cancer · 45
INTS6/DICE1 inhibits growth of human androgen-independent prostate cancer cells by altering the cell cycle profile and Wnt signaling
2009 · Stephanie Filleur, Jennifer Hirsch, et al. · Cancer Cell International · 42
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Genetic alterations of the tumor suppressor gene PTEN/MMAC1 in human brain metastases.
1999 · M Hahn, I Wieland, et al. · PubMed · 42
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome
2007 · I Wieland, C Weidner, et al. · Clinical Genetics · 41
Allelic deletion mapping on chromosome 5 in human carcinomas.
1996 · I Wieland, M Böhm, et al. · PubMed · 39
Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia
2004 · I Wieland, P Muschke, et al. · Journal of Medical Genetics · 38
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Monoclonal antibodies NORM-1 and NORM-2 induce more normal behavior of tumor cells in vitro and reduce tumor growth in vivo
1985 · H.Peter Vollmers, Beat A. Imhof, et al. · Cell · 37
Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer
2005 · Albrecht Röpke, Peter Buhtz, et al. · Oncogene · 36
Deletion analysis at the DEL‐27, APC and MTS1 loci in bladder cancer: LOH at the DEL‐27 locus on 5p13‐12 is a prognostic marker of tumor progression
1997 · Malte Böhm, Heide Kirch, et al. · International Journal of Cancer · 34
Infrequent genetic alterations of the tumor suppressor gene PTEN/MMAC1 in squamous cell carcinoma of the oral cavity
2002 · A. Mavros, M. Hahn, et al. · Journal of Oral Pathology and Medicine · 33
Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic
2007 · Ilse Wieland, Roman Makarov, et al. · European Journal of Human Genetics · 30
Works count: 112
Citation count: 2,448
H-index: 27
I10-index: 53
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