S. Jenisch

发表

Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C.

James T. Elder, N. Schork, J. Voorhees, 2000, American journal of human genetics.

The genetics of psoriasis 2001: the odyssey continues.

James T. Elder, J. Voorhees, P. Stuart, 2001, Archives of dermatology.

Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene.

Stefan Jenisch, Michael Weichenthal, Gonçalo R Abecasis, 2006, American journal of human genetics.

The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs.

Stefan Jenisch, Mark J. Daly, Colin D. Veal, 2003, American journal of human genetics.

Linkage analysis of human leukocyte antigen (HLA) markers in familial psoriasis: strong disequilibrium effects provide evidence for a major determinant in the HLA-B/-C region.

James T. Elder, S. W. Guo, J. Voorhees, 1998, American journal of human genetics.

WOFIE Stimulates Regulatory T Cells: A 2-Year Follow-up of Renal Transplant Recipients1

N. E. Mokhtari, N. Zavazava, S. Jenisch, 2006, Transplantation.

Filaggrin R501X and 2282del4 mutations are not associated with chronic plaque-type psoriasis in a German cohort.

James T. Elder, M. Weichenthal, S. Schreiber, 2007, The Journal of investigative dermatology.

HLA-DRB1 and Anti-Cyclic Citrullinated Peptide Antibody Production in Rheumatoid Arthritis

S. Jenisch, J. Steinmann, M. Marget, 2005, International Archives of Allergy and Immunology.

Peripheral multifocal chorioretinitis with panuveitis: clinical and immunogenetic characterization in older patients

S. Jenisch, E. Westphal, B. Nölle, 1998, Graefe's Archive for Clinical and Experimental Ophthalmology.

Scanning chromosome 17 for psoriasis susceptibility: lack of evidence for a distal 17q locus.

James T. Elder, E. Lange, J. Voorhees, 1995, Human heredity.

Extramedullary manifestation of a donor-derived acute myeloid leukemia in a liver transplant patient

R. Siebert, B. Dörken, C. Schoch, 2004, Leukemia.

Integration of amplified BCR/ABL fusion genes into the short arm of chromosome 17 as a novel mechanism of disease progression in chronic myeloid leukemia

R. Siebert, L. Harder, S. Gesk, 2001, Genes, chromosomes & cancer.

Nonelectrophoretic method for high-throughput HLA-DRB1 group genotyping.

J. Hampe, Carl Manaster, M. Nagy, 2004, BioTechniques.

Bypassing hybridoma technology: HLA-C reactive human single-chain antibody fragments (scFv) derived from a synthetic phage display library (HuCAL) and their potential to discriminate HLA class I specificities.

M. Tesar, D. Kabelitz, M. Krönke, 2000, Tissue antigens.

Protein-Truncation Mutations in the RP 2 Gene in a North American Cohort of Families with X-Linked Retinitis Pigmentosa

James T. Elder, J. Voorhees, P. Stuart, 1999 .

Semiquantitative reverse transcription polymerase chain reaction analysis for detection of bcr/abl rearrangement using RNA extracts from bone marrow aspirates compared with glass slide smears after 0, 2 and 4 d of storage

T. Haferlach, M. Kneba, S. Jenisch, 2001, British journal of haematology.

Routinely Prepared Cells for Cytogenetic Analysis Stored at −20 °C for Several Years can be Used for RT-PCR-Based Detection of Chromosomal Aberrations in Leukemias

T. Haferlach, M. Krönke, B. Schlegelberger, 1998 .

Detection of Minimal Residual Disease on Bone Marrow Smears by Reverse Transcriptase Polymerase Chain Reaction

T. Haferlach, S. Jenisch, H. Löffler, 1997 .

Variations in the HCR (Pg8) gene are unlikely to be causal for familial psoriasis.

James T. Elder, J. Voorhees, P. Stuart, 2001, The Journal of investigative dermatology.

Tracing antigen signatures in the human IgE repertoire

R. Valenta, D. Kabelitz, M. Novatchkova, 2010, Molecular Immunology.

WOFIE synergizes with calcineurin-inhibitor treatment and early steroid withdrawal in kidney transplantation1

B. Kremer, N. E. El Mokhtari, N. Zavazava, 2003, Transplantation.

DNA-based HLA class II postmortem typing: evaluation of different techniques for prospective corneal allografting

G. Duncker, B. Nölle, S. Jenisch, 1995, Graefe's Archive for Clinical and Experimental Ophthalmology.

Simultaneous Onset of Psoriasis Vulgaris in Monozygotic Twins

U. Mrowietz, E. Christophers, S. Jenisch, 2001, American journal of clinical dermatology.

Analysis of phenotypic variation in psoriasis as a function of age at onset and family history

James T. Elder, J. Voorhees, P. Stuart, 2002, Archives of Dermatological Research.

Evidence for two psoriasis susceptibility loci (HLA and 17q) and two novel candidate regions (16q and 20p) by genome-wide scan.

James T. Elder, J. Voorhees, P. Stuart, 1997, Human molecular genetics.

Corneodesmosin gene polymorphism demonstrates strong linkage disequilibrium with HLA and association with psoriasis vulgaris.

James T. Elder, J. Voorhees, R. Nair, 1999, Tissue antigens.

Polymorphisms of the IL12B and IL23R genes are associated with psoriasis.

Stefan Jenisch, Stefan Schreiber, Michael Weichenthal, 2008, The Journal of investigative dermatology.

Analysis of RUNX1 binding site and RAPTOR polymorphisms in psoriasis: no evidence for association despite adequate power and evidence for linkage

James T. Elder, Z. Qin, M. Weichenthal, 2005, Journal of Medical Genetics.

HLA DPA1/DPB1 genotype and haplotype frequencies, and linkage disequilibria in Nigeria, Liberia, and Gabon.

P. Kremsner, C. Meyer, F. Mockenhaupt, 1998, Tissue antigens.

Increased prevalence of the metabolic syndrome in patients with moderate to severe psoriasis

M. Weichenthal, E. Christophers, S. Jenisch, 2006, Archives of Dermatological Research.

Experience with Allogeneic Leukocyte Immunization (Ai) for Implantation Failure in the In‐Vitro Fertilization Program

S. Jenisch, D. Kabelitz, C. Kling, 2002 .

New strategies for efficient typing of HLA class-II loci DQB1 and DRB1 by using Pyrosequencing.

J. Hampe, P. Nürnberg, M. Toliat, 2005, Tissue antigens.

Linkage disequilibrium analysis of familial psoriasis: identification of multiple disease-associated MHC haplotypes.

James T. Elder, J. Voorhees, P. Stuart, 1999, Tissue antigens.

Lack of association between NOD2 3020InsC frameshift mutation and psoriasis.

James T. Elder, J. Voorhees, Y. Ogura, 2001, The Journal of investigative dermatology.

Protein tyrosine phosphatase gene PTPN22 polymorphism in psoriasis: lack of evidence for association.

Zhaohui S. Qin, James T. Elder, G. Abecasis, 2005, The Journal of investigative dermatology.

Glass slide smears are a suitable source for RT‐PCR‐based analysis of chromosomal aberrations in leukaemias

T. Haferlach, S. Jenisch, H. Löffler, 1996, British journal of haematology.

S100A2 coding sequence polymorphism: characterization and lack of association with psoriasis

James T. Elder, J. Voorhees, P. Stuart, 2001, Clincal and Experimental Dermatology.

CARD15 mutations in patients with plaque-type psoriasis and psoriatic arthritis: lack of association

James T. Elder, M. Weichenthal, J. Hampe, 2006, Archives of Dermatological Research.

Linkage disequilibrium analysis of familial

P. Stuart, E. Christophers, T. Henseler, 1999 .

Combined segregation and linkage analysis of HLA markers in familial psoriasis

James T. Elder, E. Lange, J. Voorhees, 2002, European Journal of Human Genetics.

The MHC genes in psoriasis

James T. Elder, M. Weichenthal, J. Voorhees, 2005 .

Reply to Leder and Hodge

James T. Elder, J. Voorhees, P. Stuart, 1999 .

Sequence and Haplotype Analysis Supports Hla-c as the Psoriasis Susceptibility 1 Gene Dermatology And

P. Stuart, R. Nair, S. Jenisch, 2022 .