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Jörg Epplen

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Physiology

Geographic Areas

Germany

Genes & Molecular Sequences

Procedures

Concepts & Ideas

Chemicals & Drugs

Phenomena

Single-Stranded Conformational Polymorphism

Disorders

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Publications

TOP 3
Wieczorek S; Hoffjan S; Chan A; Rey L; Harper L; Fricke H; Holle J U; Gross W L; Epplen J T; Lamprecht P
Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients.
Yu X; Wieczorek S; Franke A; Yin H; Pierer M; Sina C; Karlsen T H; Boberg K M; Bergquist A; Kunz M; Witte T; Gross W L; Epplen J T; Alarcón-Riquelme M E; Schreiber S; Ibrahim S M
Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases.
Stemmler S; Nothnagel M; Parwez Q; Petrasch-Parwez E; Epplen J T; Hoffjan S
Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.

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All Publications

2009: Wieczorek S; Hoffjan S; Chan A; Rey L; Harper L; Fricke H; Holle J U; Gross W L; Epplen J T; Lamprecht P
Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients.
Genes and immunity 2009;10(6):591-5.
2009: Yu X; Wieczorek S; Franke A; Yin H; Pierer M; Sina C; Karlsen T H; Boberg K M; Bergquist A; Kunz M; Witte T; Gross W L; Epplen J T; Alarcón-Riquelme M E; Schreiber S; Ibrahim S M
Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases.
Genes and immunity 2009;10(6):601-5.
2009: Stemmler S; Nothnagel M; Parwez Q; Petrasch-Parwez E; Epplen J T; Hoffjan S
Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.
International journal of immunogenetics 2009;36(4):217-22.
2009: Glas Jürgen; Stallhofer Johannes; Ripke Stephan; Wetzke Martin; Pfennig Simone; Klein Wolfram; Epplen Jörg T; Griga Thomas; Schiemann Uwe; Lacher Martin; Koletzko Sibylle; Folwaczny Matthias; Lohse Peter; Göke Burkhard; Ochsenkühn Thomas; Müller-Myhsok Bertram; Brand Stephan
Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.
The American journal of gastroenterology 2009;104(7):1737-44.
2009: Lamprecht Peter; Wieczorek Stefan; Epplen Jörg T; Ambrosch Petra; Kallenberg Cees G M
Granuloma formation in ANCA-associated vasculitides.
APMIS. Supplementum 2009;(127):32-6.
2009: Glas Jürgen; Seiderer Julia; Pasciuto Giulia; Tillack Cornelia; Diegelmann Julia; Pfennig Simone; Konrad Astrid; Schmechel Silke; Wetzke Martin; Török Helga-Paula; Stallhofer Johannes; Jürgens Matthias; Griga Thomas; Klein Wolfram; Epplen Jörg T; Schiemann Uwe; Mussack Thomas; Lohse Peter; Göke Burkhard; Ochsenkühn Thomas; Folwaczny Matthias; Müller-Myhsok Bertram; Brand Stephan
rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
The American journal of gastroenterology 2009;104(3):665-72.
2009: Akkad D A; Hoffjan S; Petrasch-Parwez E; Beygo J; Gold R; Epplen J T
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients.
Journal of autoimmunity 2009;32(2):110-5.
2009: Beygo Jasmin; Parwez Qumar; Petrasch-Parwez Elisabeth; Epplen Jörg T; Hoffjan Sabine
No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohort.
Molecular and cellular probes 2009;23(1):16-9.
2009: Arinir U; Hoffjan S; Knoop H; Schultze-Werninghaus G; Epplen J T; Rohde G
[The genetics of chronic obstructive pulmonary disease]
Pneumologie (Stuttgart, Germany) 2009;63(1):41-8.
2009: Wieczorek Stefan; Knaup Silvia; Gross Wolfgang L; Epplen Jörg T
Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis.
PPAR research 2009;2009():786781.
2008: Klinge Lars; Dekomien Gabriele; Aboumousa Ahmed; Charlton Richard; Epplen Jörg T; Barresi Rita; Bushby Kate; Straub Volker
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?
Neuromuscular disorders : NMD 2008;18(12):934-41.
2008: Arning Larissa; Schöls Ludger; Cin Huriye; Souquet Manfred; Epplen Jörg T; Timmann Dagmar
Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).
Neurogenetics 2008;9(4):295-9.
2008: Heckmann M; Holle J U; Arning L; Knaup S; Hellmich B; Nothnagel M; Jagiello P; Gross W L; Epplen J T; Wieczorek S
The Wegener's granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping.
Annals of the rheumatic diseases 2008;67(7):972-9.
2008: Wieczorek S; Hellmich B; Arning L; Moosig F; Lamprecht P; Gross W L; Epplen J T
Functionally relevant variations of the interleukin-10 gene associated with antineutrophil cytoplasmic antibody-negative Churg-Strauss syndrome, but not with Wegener's granulomatosis.
Arthritis and rheumatism 2008;58(6):1839-48.
2008: Schöls Ludger; Arning Larissa; Schüle Rebecca; Epplen Jörg T; Timmann Dagmar
"Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2).
Journal of neurology 2008;255(4):495-501.
2008: Arning Larissa; Monté Didier; Hansen Wiebke; Wieczorek Stefan; Jagiello Peter; Akkad Denis A; Andrich Jürgen; Kraus Peter H; Saft Carsten; Epplen Jörg T
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease.
Journal of molecular medicine (Berlin, Germany) 2008;86(4):485-90.
2008: Adrian Oliver; Kaiser Sylvia; Sachser Norbert; Jandewerth Pia; Löttker Petra; Epplen Jörg T; Hennessy Michael B
Female influences on pair formation, reproduction and male stress responses in a monogamous cavy (Galea monasteriensis).
Hormones and behavior 2008;53(3):403-12.
2008: Glas Jürgen; Konrad Astrid; Schmechel Silke; Dambacher Julia; Seiderer Julia; Schroff Frieder; Wetzke Martin; Roeske Darina; Török Helga-Paula; Tonenchi Laurian; Pfennig Simone; Haller Dirk; Griga Thomas; Klein Wolfram; Epplen Jörg T; Folwaczny Christian; Lohse Peter; Göke Burkhard; Ochsenkühn Thomas; Mussack Thomas; Folwaczny Matthias; Müller-Myhsok Bertram; Brand Stephan
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
The American journal of gastroenterology 2008;103(3):682-91.
2008: Münch Christoph; Epplen Jörg T; Meins Moritz; Meyer Robert; Weber Jörg R; Meyer Thomas
Severe Guillain-Barré syndrome associated with chromosome 17p11.2-12 duplication.
Muscle & nerve 2008;37(2):256-8.
2008: Börgel Jan; Bulut Daniel; Hanefeld Christoph; Neubauer Horst; Mügge Andreas; Epplen Jörg T; Holland-Letz Tim; Spiecker Martin
The CYP2J2 G-50T polymorphism and myocardial infarction in patients with cardiovascular risk profile.
BMC cardiovascular disorders 2008;8():41.
2008: Akkad Denis A; Kruse Niels; Arning Larissa; Gold Ralf; Epplen Jörg T
Genomic NGFB variation and multiple sclerosis in a case control study.
BMC medical genetics 2008;9():107.
2008: Parwez Qumar; Stemmler Susanne; Epplen Jörg T; Hoffjan Sabine
Variation in genes encoding eosinophil granule proteins in atopic dermatitis patients from Germany.
Journal of negative results in biomedicine 2008;7():9.
2008: Schlang Katharina J; Arning Larissa; Epplen Joerg T; Stemmler Susanne
Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).
BMC medical genetics 2008;9():71.
2007: Akkad D A; Arning L; Ibrahim S M; Epplen J T
Sex specifically associated promoter polymorphism in multiple sclerosis affects interleukin 4 expression levels.
Genes and immunity 2007;8(8):703-6.
2007: Lampert Kathrin P; Lamatsch Dunja K; Fischer Petra; Epplen Jörg T; Nanda Indrajit; Schmid Michael; Schartl Manfred
Automictic reproduction in interspecific hybrids of poeciliid fish.
Current biology : CB 2007;17(22):1948-53.
2007: Janko Karel; Bohlen Jörg; Lamatsch Dunja; Flajshans Martin; Epplen Jörg T; Ráb Petr; Kotlík Petr; Slechtová Vera
The gynogenetic reproduction of diploid and triploid hybrid spined loaches (Cobitis: Teleostei), and their ability to establish successful clonal lineages--on the evolution of polyploidy in asexual vertebrates.
Genetica 2007;131(2):185-94.
2007: Arning Larissa; Saft Carsten; Wieczorek Stefan; Andrich Jürgen; Kraus Peter H; Epplen Jörg T
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.
Human genetics 2007;122(2):175-82.
2007: Blaszczyk W M; Distler C; Dekomien G; Arning L; Hoffmann K-P; Epplen J T
Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo).
Animal genetics 2007;38(4):421-3.
2007: Macaluso Filippina; Nothnagel Michael; Parwez Qumar; Petrasch-Parwez Elisabeth; Bechara Falk Georges; Epplen Joerg Thomas; Hoffjan Sabine
Polymorphisms in NACHT-LRR (NLR) genes in atopic dermatitis.
Experimental dermatology 2007;16(8):692-8.
2007: Schmoll T; Schurr F M; Winkel W; Epplen J T; Lubjuhn T
Polyandry in coal tits Parus ater: fitness consequences of putting eggs into multiple genetic baskets.
Journal of evolutionary biology 2007;20(3):1115-25.
2007: Glas Jürgen; Török Helga-Paula; Tonenchi Laurian; Wetzke Martin; Beynon Vanessa; Teshome Molla Y; Cotofana Sebastian; Schiemann Uwe; Griga Thomas; Klein Wolfram; Epplen Joerg T; Folwaczny Christian; Folwaczny Matthias; Mussack Thomas; Weiss Elisabeth H
The 14-bp deletion polymorphism in the HLA-G gene displays significant differences between ulcerative colitis and Crohn's disease and is associated with ileocecal resection in Crohn's disease.
International immunology 2007;19(5):621-6.
2007: Vonend Oliver; Altenhenne Christian; Büchner Nicolaus J; Dekomien Gabriele; Maser-Gluth Christiane; Weiner Stefan M; Sellin Lorenz; Hofebauer Stefan; Epplen Jörg T; Rump Lars C
A German family with glucocorticoid-remediable aldosteronism.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007;22(4):1123-30.
2007: Stemmler Susanne; Parwez Qumar; Petrasch-Parwez Elisabeth; Epplen Joerg T; Hoffjan Sabine
Two common loss-of-function mutations within the filaggrin gene predispose for early onset of atopic dermatitis.
The Journal of investigative dermatology 2007;127(3):722-4.
2007: Glas Jürgen; Seiderer Julia; Wetzke Martin; Konrad Astrid; Török Helga-Paula; Schmechel Silke; Tonenchi Laurian; Grassl Christine; Dambacher Julia; Pfennig Simone; Maier Kerstin; Griga Thomas; Klein Wolfram; Epplen Jörg T; Schiemann Uwe; Folwaczny Christian; Lohse Peter; Göke Burkhard; Ochsenkühn Thomas; Müller-Myhsok Bertram; Folwaczny Matthias; Mussack Thomas; Brand Stephan
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
PloS one 2007;2(9):e819.
2007: Schimming Tobias T; Parwez Qumar; Petrasch-Parwez Elisabeth; Nothnagel Michael; Epplen Joerg T; Hoffjan Sabine
Association of toll-interacting protein gene polymorphisms with atopic dermatitis.
BMC dermatology 2007;7():3.
2007: Bartels Nina K; Börgel Jan; Wieczorek Stefan; Büchner Nikolaus; Hanefeld Christoph; Bulut Daniel; Mügge Andreas; Rump Lars C; Sanner Bernd M; Epplen Jörg T
Risk factors and myocardial infarction in patients with obstructive sleep apnea: impact of beta2-adrenergic receptor polymorphisms.
BMC medicine 2007;5():1.
2006: Hoffjan S; Parwez Q; Petrasch-Parwez E; Falkenstein D; Nothnagel M; Epplen J T
Association screen for atopic dermatitis candidate gene regions using microsatellite markers in pooled DNA samples.
International journal of immunogenetics 2006;33(6):401-9.
2006: Hoffjan Sabine; Thiels Charlotte; Vorgerd Matthias; Neuen-Jacob Eva; Epplen Jörg T; Kress Wolfram
Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1.
Neuromuscular disorders : NMD 2006;16(11):749-53.
2006: Akkad Denis A; Gödde René; Epplen Jörg T
No association between synapsin III gene promoter polymorphisms and multiple sclerosis in German patients.
Journal of neurology 2006;253(10):1365-6.
2006: Rommel Oliver; Kley Rudolf A; Dekomien Gabriele; Epplen Jörg T; Vorgerd Matthias; Hasenbring Monika
Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related coping.
Pain 2006;124(3):295-304.
2006: Bach K; Preyer J; Jensen A; Epplen J T; Kunstmann E
[Gynecological outpatient management in HNPCC]
Zentralblatt für Gynäkologie 2006;128(4):207-12.
2006: Glas Jürgen; Török Helga-Paula; Tonenchi Laurian; Müller-Myhsok Bertram; Mussack Thomas; Wetzke Martin; Klein Wolfram; Epplen Joerg T; Griga Thomas; Schiemann Uwe; Lohse Peter; Seiderer Julia; Schnitzler Fabian; Brand Stephan; Ochsenkühn Thomas; Folwaczny Matthias; Folwaczny Christian
Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes.
Inflammatory bowel diseases 2006;12(7):606-11.
2006: Schlitter A M; Woitalla D; Mueller T; Epplen J T; Dekomien G
The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany.
Journal of neurology, neurosurgery, and psychiatry 2006;77(7):891-2.
2006: Zunker Katrin; Epplen Jörg T; Schartl Manfred
Genomic stability in malignant melanoma of Xiphophorus.
Melanoma research 2006;16(2):105-13.
2006: Felderbauer P; Klein W; Bulut K; Ansorge N; Dekomien G; Werner I; Epplen J T; Schmitz F; Schmidt W E
Mutations in the calcium-sensing receptor: a new genetic risk factor for chronic pancreatitis?
Scandinavian journal of gastroenterology 2006;41(3):343-8.
2006: Gödde René; Akkad Denis-Amer; Arning Larissa; Dekomien Gabriele; Herchenbach Julia; Kunstmann Erdmute; Meins Moritz; Wieczorek Stefan; Epplen Jörg T; Hoffjan Sabine
Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.
Electrophoresis 2006;27(5-6):939-46.
2006: Akkad D A; Jagiello P; Szyld P; Goedde R; Wieczorek S; Gross W L; Epplen J T
Promoter polymorphism rs3087456 in the MHC class II transactivator gene is not associated with susceptibility for selected autoimmune diseases in German patient groups.
International journal of immunogenetics 2006;33(1):59-61.
2006: Müller Annegret; Schackert Hans K; Lange Bettina; Rüschoff Josef; Füzesi Laslow; Willert Joerg; Burfeind Peter; Shah Parantu; Becker Heinz; Epplen Joerg Thomas; Stemmler Susanne
A novel MSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years.
American journal of medical genetics. Part A 2006;140(3):195-9.
2006: Schlitter A M; Kurz M; Larsen J P; Woitalla D; Müller T; Epplen J T; Dekomien G
Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts.
Acta neurologica Scandinavica 2006;113(1):9-13.
2006: Börgel Jan; Schulz Tino; Bartels Nina K; Epplen Jörg T; Büchner Nikolaus; Rump Lars Christian; Huesing Anika; Sanner Bernd M; Mügge Andreas
Modifying effects of the R389G beta1-adrenoceptor polymorphism on resting heart rate and blood pressure in patients with obstructive sleep apnoea.
Clinical science (London, England : 1979) 2006;110(1):117-23.
2006: Mai Maren; Akkad Amer D; Wieczorek Stefan; Saft Carsten; Andrich Jürgen; Kraus Peter H; Epplen Jörg T; Arning Larissa
No association between polymorphisms in the BDNF gene and age at onset in Huntington disease.
BMC medical genetics 2006;7():79.
2006: Engelfried Kathrin; Vorgerd Matthias; Hagedorn Michaela; Haas Gerhard; Gilles Jürgen; Epplen Jörg T; Meins Moritz
Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).
BMC medical genetics 2006;7():53.
2006: Szyld Pawel; Jagiello Peter; Csernok Elena; Gross Wolfgang L; Epplen Joerg T
On the Wegener granulomatosis associated region on chromosome 6p21.3.
BMC medical genetics 2006;7():21.
2006: Wieczorek Stefan; Arning Larissa; Alheite Ingrid; Epplen Jörg T
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.
Journal of human genetics 2006;51(4):363-7.
2006: Sprengelmeyer R; Schroeder U; Young A W; Epplen J T
Disgust in pre-clinical Huntington's disease: a longitudinal study.
Neuropsychologia 2006;44(4):518-33.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):543.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):543.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):541-2.
2005: Dekomien G; Gencik M; Gencikova A; Klenk Y; Epplen J T
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):541.
2005: Jagiello Peter; Aries Peer; Arning Larissa; Wagenleiter Sonja E N; Csernok Elena; Hellmich Bernhard; Gross Wolfgang L; Epplen Joerg T
The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.
Arthritis and rheumatism 2005;52(12):4039-43.
2005: Petrasch-Parwez Elisabeth; Saft Carsten; Schlichting Annegrit; Andrich Jürgen; Napirei Markus; Arning Larissa; Wieczorek Stefan; Dermietzel Rolf; Epplen Jörg Thomas
Is the retina affected in Huntington disease?
Acta neuropathologica 2005;110(5):523-5.
2005: Arning Larissa; Kraus Peter H; Saft Carsten; Andrich Jürgen; Epplen Jörg T
Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD).
BMC medical genetics 2005;6():35.
2005: Wagenleiter S E N; Klein W; Griga T; Schmiegel W; Epplen J T; Jagiello P
A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease.
International journal of immunogenetics 2005;32(5):323-4.
2005: Vogler Susanne; Goedde René; Miterski Bianca; Gold Ralf; Kroner Antje; Koczan Dirk; Zettl Uwe-Klaus; Rieckmann Peter; Epplen Joerg T; Ibrahim Saleh M
Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis.
Journal of molecular medicine (Berlin, Germany) 2005;83(10):806-11.
2005: Török H-P; Glas J; Tonenchi L; Lohse P; Müller-Myhsok B; Limbersky O; Neugebauer C; Schnitzler F; Seiderer J; Tillack C; Brand S; Brünnler G; Jagiello P; Epplen J T; Griga T; Klein W; Schiemann U; Folwaczny M; Ochsenkühn T; Folwaczny C
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.
Gut 2005;54(10):1421-7.
2005: Hoffjan Sabine; Stemmler Susanne; Parwez Qumar; Petrasch-Parwez Elisabeth; Arinir Umut; Rohde Gernot; Reinitz-Rademacher Karin; Schultze-Werninghaus Gerhard; Bufe Albrecht; Epplen Jörg T
Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.
BMC medical genetics 2005;6():34.
2005: Alber Burkhard; Pernauer Magdalena; Schwan Annemarie; Rothmund Gabriele; Hoffmann Karl T; Brummer Dagmar; Sperfeld Anne D; Uttner Ingo; Binder Heinrich; Epplen Joerg T; Dullinger Jörn; Ludolph Albert C; Meyer Thomas
Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.
Journal of the neurological sciences 2005;236(1-2):9-12.
2005: Hoffjan Sabine; Epplen Jörg T
The genetics of atopic dermatitis: recent findings and future options.
Journal of molecular medicine (Berlin, Germany) 2005;83(9):682-92.
2005: Kunstmann E; Hildmann A; Lautermann J; Aletsee C; Epplen J T; Sudhoff H
[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling]
HNO 2005;53(9):773-8.
2005: Arinir Umut; Klein Wolfram; Rohde Gernot; Stemmler Susanne; Epplen Joerg T; Schultze-Werninghaus Gerhard
Polymorphisms in the interleukin-8 gene in patients with chronic obstructive pulmonary disease.
Electrophoresis 2005;26(15):2888-91.
2005: Bach K; Hüppe D; Schmiegel W; Epplen J T; Kunstmann E
[Evaluation of outpatient management in HNPCC]
Zeitschrift für Gastroenterologie 2005;43(7):647-51.
2005: Gödde René; Rohde Klaus; Becker Christian; Toliat Mahammad R; Entz Patricia; Suk Anita; Müller Norbert; Sindern Eckhart; Haupts Michael; Schimrigk Sebastian; Nürnberg Peter; Epplen Jörg T
Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips.
Journal of molecular medicine (Berlin, Germany) 2005;83(6):486-94.
2005: Wieczorek S W; Epplen J T
Gene symbol: PANK2. Disease: Pantothenate kinase associated neurodegeneration (PKAN).
Human genetics 2005;116(6):545.
2005: Wieczorek S; Epplen J T
Gene symbol: PANK2. Disease: Pantothenate kinase associated neurodegeneration (PKAN).
Human genetics 2005;116(6):535.
2005: Griga T; Wilkens C; Schmiegel W; Folwaczny C; Hagedorn M; Duerig N; Epplen J; Klein W
Association between the promoter polymorphism T/C at position -159 of the CD14 gene and anti-inflammatory therapy in patients with inflammatory bowel disease.
European journal of medical research 2005;10(5):183-6.
2005: Schrameyer Tanja; Dekomien Gabriele; Pasternack Sandra M; Reinartz Benedikt S; Santos Eduardo J M; Epplen Jörg T
Long- and short-haired Weimaraner dogs represent two populations of one breed.
Electrophoresis 2005;26(9):1668-72.
2005: Stemmler S; Arinir U; Klein W; Rohde G; Hoffjan S; Wirkus N; Reinitz-Rademacher K; Bufe A; Schultze-Werninghaus G; Epplen J T
Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.
Genes and immunity 2005;6(3):225-30.
2005: Lampert Kathrin P; Lamatsch Dunja K; Epplen Jörg T; Schartl Manfred
Evidence for a monophyletic origin of triploid clones of the Amazon molly, Poecilia formosa.
Evolution; international journal of organic evolution 2005;59(4):881-9.
2005: Blaszczyk Wanda M; Arning Larissa; Hoffmann Klaus-Peter; Epplen Joerg T
A Tyrosinase missense mutation causes albinism in the Wistar rat.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2005;18(2):144-5.
2005: Klein W; Tromm A; Folwaczny C; Hagedorn M; Duerig N; Epplen J; Schmiegel W; Griga T
The G2964A polymorphism of the STAT6 gene in inflammatory bowel disease.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2005;37(3):159-61.
2005: Schmoll Tim; Dietrich Verena; Winkel Wolfgang; Epplen Jörg T; Schurr Frank; Lubjuhn Thomas
Paternal genetic effects on offspring fitness are context dependent within the extrapair mating system of a socially monogamous passerine.
Evolution; international journal of organic evolution 2005;59(3):645-57.
2005: Arning Larissa; Kraus Peter H; Valentin Sandra; Saft Carsten; Andrich Jürgen; Epplen Jörg T
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease.
Neurogenetics 2005;6(1):25-8.
2005: Meins M; Lehmann J; Gerresheim F; Herchenbach J; Hagedorn M; Hameister K; Epplen J T
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome.
Journal of medical genetics 2005;42(2):e12.
2005: Jagiello P; Klein W; Schultz H; Csernok E; Gross W L; Epplen J T
Association study of Wegener granulomatosis and the functionally relevant A645G polymorphism in the bactericidal/permeability increasing protein (BPI) gene.
International journal of immunogenetics 2005;32(1):3-6.
2005: Felderbauer P; Hoffmann P; Klein W; Bulut K; Ansorge N; Epplen J T; Schmitz F; Schmidt W E
Identification of a novel calcium-sensing receptor gene mutation causing familial hypocalciuric hypercalcemia by single-strand conformation polymorphism analysis.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2005;113(1):31-4.
2005: Jagiello Peter; Gross Wolfgang L; Epplen Jörg T
Complex genetics of Wegener granulomatosis.
Autoimmunity reviews 2005;4(1):42-7.
2005: Meins Moritz; Hagh Javad Karimzad; Gerresheim Fritz; Einhoff Elisabeth; Olschewski Heidi; Strehl Henning; Epplen Jörg T
Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
American journal of medical genetics. Part A 2005;132A(1):84-9.
2005: Hansen Wiebke; Saft Carsten; Andrich Jürgen; Müller Thomas; Wieczorek Stefan; Epplen Jörg T; Arning Larissa
Failure to confirm influence of methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease.
Journal of negative results in biomedicine 2005;4():12.
2005: Schlitter Anna Melissa; Kurz Martin; Larsen Jan P; Woitalla Dirk; Mueller Thomas; Epplen Joerg T; Dekomien Gabriele
Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations.
Journal of negative results in biomedicine 2005;4():10.
2005: Wagenleiter Sonja E N; Jagiello Peter; Akkad Denis A; Arning Larissa; Griga Thomas; Klein Wolfram; Epplen Jörg T
On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors.
Journal of negative results in biomedicine 2005;4():8.
2005: Gödde René; Brune Stefanie; Jagiello Peter; Sindern Eckhart; Haupts Michael; Schimrigk Sebastian; Müller Norbert; Epplen Jörg T
An extended association screen in multiple sclerosis using 202 microsatellite markers targeting apoptosis-related genes does not reveal new predisposing factors.
Journal of negative results in biomedicine 2005;4():7.
2005: Jagiello Peter; Wieczorek Stefan; Yu Philipp; Csernok Elena; Gross Wolfgang L; Epplen Joerg T
Association study with Wegener granulomatosis of the human phospholipase Cgamma2 gene.
Journal of negative results in biomedicine 2005;4():1.
2004: Serrano-Fernández P; Ibrahim S M; Zettl U K; Thiesen H-J; Gödde R; Epplen J T; Möller S
Intergenomic consensus in multifactorial inheritance loci: the case of multiple sclerosis.
Genes and immunity 2004;5(8):615-20.
2004: Saft C; Andrich J E; Brune N; Gencik M; Kraus P H; Przuntek H; Epplen J T
Apolipoprotein E genotypes do not influence the age of onset in Huntington's disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(12):1692-6.
2004: Petrasch-Parwez Elisabeth; Habbes Hans-Werner; Weickert Svenja; Löbbecke-Schumacher Marlen; Striedinger Katherine; Wieczorek Stefan; Dermietzel Rolf; Epplen Joerg Thomas
Fine-structural analysis and connexin expression in the retina of a transgenic model of Huntington's disease.
The Journal of comparative neurology 2004;479(2):181-97.
2004: Wieczorek Stefan; Jagiello Peter; Arning Larissa; Dahmen Norbert; Epplen Joerg T
Screening for candidate gene regions in narcolepsy using a microsatellite based approach and pooled DNA.
Journal of molecular medicine (Berlin, Germany) 2004;82(10):696-705.
2004: Gödde René; Nigmatova Viktoria; Jagiello Peter; Sindern Eckhart; Haupts Michael; Schimrigk Sebastian; Epplen Jörg T
Refining the results of a whole-genome screen based on 4666 microsatellite markers for defining predisposition factors for multiple sclerosis.
Electrophoresis 2004;25(14):2212-8.
2004: Kunstmann Erdmute; Vieland Judith; Brasch Frank E; Hahn Stephan A; Epplen Joerg T; Schulmann Karsten; Schmiegel Wolff
HNPCC: six new pathogenic mutations.
BMC medical genetics 2004;5():16.
2004: Walter M C; Dekomien G; Schlotter-Weigel B; Reilich P; Pongratz D; Müller-Felber W; Epplen J T; Huebner A; Lochmüller H
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2004;23(1):1-5.
2004: Jagiello Peter; Gencik Martin; Arning Larissa; Wieczorek Stefan; Kunstmann Erdmute; Csernok Elena; Gross Wolfgang L; Epplen Joerg T
New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes.
Human genetics 2004;114(5):468-77.
2004: Wieczorek S; Dahmen N; Kasten M; Epplen J T; Gencik M
A rare form of narcolepsy (HLA-DR2-) shows possible association with (functionally relevant) alpha-interferon gene polymorphisms.
Psychiatric genetics 2004;14(1):47-51.
2004: Arning Larissa; Jagiello Peter; Wieczorek Stefan; Saft Carsten; Andrich Jürgen; Epplen Jörg T
Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease.
BMC medical genetics 2004;5():7.
2004: Klein Wolfram; Rohde Gernot; Arinir Umut; Hagedorn Michaela; Dürig Natascha; Schultze-Werninghaus Gerhard; Epplen Jörg T
A promotor polymorphism in the Interleukin 11 gene is associated with chronic obstructive pulmonary disease.
Electrophoresis 2004;25(6):804-8.
2004: Klein Wolfram; Tromm Andreas; Folwaczny Christian; Hagedorn Michaela; Duerig Natascha; Epplen Joerg T; Schmiegel Wolff H; Griga Thomas
A polymorphism of the NFKBIA gene is associated with Crohn's disease patients lacking a predisposing allele of the CARD15 gene.
International journal of colorectal disease 2004;19(2):153-6.
2004: Miterski Bianca; Drynda Susanne; Böschow Gundula; Klein Wolfram; Oppermann Joachim; Kekow Jörn; Epplen Jörg Thomas
Complex genetic predisposition in adult and juvenile rheumatoid arthritis.
BMC genetics 2004;5():2.
2004: Arning Larissa; Jagiello Peter; Schara Ulrike; Vorgerd Matthias; Dahmen Norbert; Gencikova Alexandra; Mortier Wilhelm; Epplen Jörg T; Gencik Martin
Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.
Journal of neurology 2004;251(1):72-8.
2004: Brune N; Andrich J; Gencik M; Saft C; Müller Th; Valentin S; Przuntek H; Epplen J T
Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's disease.
Journal of neural transmission. Supplementum 2004;(68):105-10.
2004: Lamatsch D K; Nanda I; Schlupp I; Epplen J T; Schmid M; Schartl M
Distribution and stability of supernumerary microchromosomes in natural populations of the Amazon molly, Poecilia formosa.
Cytogenetic and genome research 2004;106(2-4):189-94.
2003: Dekomien Gabriele; Epplen Jörg Thomas
Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy.
Molecular vision 2003;9():601-5.
2003: Krüger Rejko; Fischer Christian; Schulte Thorsten; Strauss Karsten M; Müller Thomas; Woitalla Dirk; Berg Daniela; Hungs Marcel; Gobbele Rene; Berger Klaus; Epplen Jörg T; Riess Olaf; Schöls Ludger
Mutation analysis of the neurofilament M gene in Parkinson's disease.
Neuroscience letters 2003;351(2):125-9.
2003: Klein W; Tromm A; Griga T; Folwaczny C; Hocke M; Eitner K; Marx M; Duerig N; Epplen J T
Interaction of polymorphisms in the CARD15 and CD14 genes in patients with Crohn disease.
Scandinavian journal of gastroenterology 2003;38(8):834-6.
2003: Schmoll Tim; Janzon Volker; Epplen Jörg T; Lubjuhn Thomas
Extra-pair sires as identified by means of standardized across-gel comparisons of multilocus DNA fingerprints.
Electrophoresis 2003;24(16):2758-63.
2003: Böhringer Stefan; Hardt Cornelia; Miterski Bianca; Steland Ansgar; Epplen Jörg T
Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data.
European journal of human genetics : EJHG 2003;11(8):573-84.
2003: Rutsch Frank; Ruf Nico; Vaingankar Sucheta; Toliat Mohammad R; Suk Anita; Höhne Wolfgang; Schauer Galen; Lehmann Mandy; Roscioli Tony; Schnabel Dirk; Epplen Jörg T; Knisely Alex; Superti-Furga Andrea; McGill James; Filippone Marco; Sinaiko Alan R; Vallance Hillary; Hinrichs Bernd; Smith Wendy; Ferre Merry; Terkeltaub Robert; Nürnberg Peter
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification.
Nature genetics 2003;34(4):379-81.
2003: Dekomien Gabriele; Epplen Joerg T
Analysis of PDE6D and PDE6G genes for generalised progressive retinal atrophy (gPRA) mutations in dogs.
Genetics, selection, evolution : GSE 2003;35(4):445-56.
2003: Schulte T; Böhringer S; Schöls L; Müller T; Fischer C; Riess O; Przuntek H; Berger K; Epplen J T; Krüger R
Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2003;110(7):749-55.
2003: Wieczorek S; Gencik M; Rujescu D; Tonn P; Giegling I; Epplen J T; Dahmen N
TNFA promoter polymorphisms and narcolepsy.
Tissue antigens 2003;61(6):437-42.
2003: Jagiello P; Hammans C; Wieczorek S; Arning L; Stefanski A; Strehl H; Epplen J T; Gencik M
A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneity.
Human mutation 2003;21(6):630-5.
2003: Schulte T; Miterski B; Börnke C; Przuntek H; Epplen J T; Schöls L
Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia.
Neurology 2003;60(9):1529-32.
2003: Kunstmann Erdmute; Hardt Cornelia; Crabtree Jean E; Suerbaum Sebastian; Epplen Jörg T
Helicobacter pylori infection: CagA-specific antibodies are associated with clinical outcome, but not with HLA-class II polymorphisms of the host.
International journal of medical microbiology : IJMM 2003;292(7-8):537-40.
2003: Schmoll Tim; Dietrich Verena; Winkel Wolfgang; Epplen Jörg T; Lubjuhn Thomas
Long-term fitness consequences of female extra-pair matings in a socially monogamous passerine.
Proceedings. Biological sciences / The Royal Society 2003;270(1512):259-64.
2003: Wieczorek Stefan; Dahmen Norbert; Jagiello Peter; Epplen Joerg T; Gencik Martin
Polymorphisms of the tumor necrosis factor receptors: no association with narcolepsy in German patients.
Journal of molecular medicine (Berlin, Germany) 2003;81(2):87-90.
2003: Dahmen N; Kasten M; Wieczorek S; Gencik M; Epplen J T; Ullrich B
Increased frequency of migraine in narcoleptic patients: a confirmatory study.
Cephalalgia : an international journal of headache 2003;23(1):14-9.
2002: Klein W; Tromm A; Griga T; Fricke H; Folwaczny C; Hocke M; Eitner K; Marx M; Duerig N; Epplen J T
A polymorphism in the IL11 gene is associated with ulcerative colitis.
Genes and immunity 2002;3(8):494-6.
2002: Dekomien Gabriele; Epplen Jörg Thomas
The canine Recoverin (RCV1) gene: a candidate gene for generalized progressive retinal atrophy.
Molecular vision 2002;8():436-41.
2002: Hohoff Christa; Solmsdorff Katrin; Löttker Petra; Kemme Kristina; Epplen Jörg T; Cooper Trevor G; Sachser Norbert
Monogamy in a new species of wild guinea pigs (Galea sp.).
Die Naturwissenschaften 2002;89(10):462-5.
2002: Goedde Rene; Sawcer Stephen; Boehringer Stefan; Miterski Bianca; Sindern Eckhart; Haupts Michael; Schimrigk Sebastian; Compston Alastair; Epplen Joerg T
A genome screen for linkage disequilibrium in HLA-DRB1*15-positive Germans with multiple sclerosis based on 4666 microsatellite markers.
Human genetics 2002;111(3):270-7.
2002: Wintermeyer P; Riess O; Schöls L; Przuntek H; Miterski B; Epplen J T; Krüger R
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patients.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(9):1181-8.
2002: Sauter S; Miterski B; Klimpe S; Bönsch D; Schöls L; Visbeck A; Papke T; Hopf H C; Engel W; Deufel T; Epplen J T; Neesen J
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
Human mutation 2002;20(2):127-32.
2002: Dekomien Gabriele; Epplen Jörg Thomas
Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy.
BMC genetics 2002;3():12.
2002: Dekomien Gabriele; Epplen Jörg Thomas
The canine Phosducin gene: characterization of the exon-intron structure and exclusion as a candidate gene for generalized progressive retinal atrophy in 11 dog breeds.
Molecular vision 2002;8():138-42.
2002: Miterski B; Böhringer S; Klein W; Sindern E; Haupts M; Schimrigk S; Epplen J T
Inhibitors in the NFkappaB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations.
Genes and immunity 2002;3(4):211-9.
2002: Andrich J; Schmitz T; Saft C; Postert T; Kraus P; Epplen J T; Przuntek H; Agelink M W
Autonomic nervous system function in Huntington's disease.
Journal of neurology, neurosurgery, and psychiatry 2002;72(6):726-31.
2002: Bauer Ingrid; Gencik Martin; Laccone Franco; Peters Hartmut; Weber Bernhard H F; Feder Elke Holinski; Weirich Helga; Morris-Rosendahl Deborah J; Rolfs Arndt; Gencikova Alexandra; Bauer Peter; Wenning Gregor K; Epplen Jörg T; Holmes Susan E; Margolis Russell L; Ross Christopher A; Riess Olaf
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.
Annals of neurology 2002;51(5):662.
2002: Miterski Bianca; Epplen Jörg T; Gencik Martin
On the genetic contribution to selected multifactorial diseases with autoimmune characteristics.
Cellular and molecular biology (Noisy-le-Grand, France) 2002;48(3):331-41.
2002: Miterski Bianca; Sindern Eckhart; Haupts Michael; Schimrigk Sebastian; Epplen Joerg T
PTPRC (CD45) is not associated with multiple sclerosis in a large cohort of German patients.
BMC medical genetics 2002;3():3.
2002: Gencik M; Hammans C; Strehl H; Wagner N; Epplen J T
Chorea Huntington: a rare case with childhood onset.
Neuropediatrics 2002;33(2):90-2.
2002: Stöck Matthias; Lamatsch Dunja K; Steinlein Claus; Epplen Jörg T; Grosse Wolf-Rüdiger; Hock Robert; Klapperstück Thomas; Lampert Kathrin P; Scheer Ulrich; Schmid Michael; Schartl Manfred
A bisexually reproducing all-triploid vertebrate.
Nature genetics 2002;30(3):325-8.
2002: Lubjuhn Thomas; Sramkova Anna; Masello Juan F; Quillfeldt Petra; Epplen Jörg Thomas
Truly hypervariable DNA fingerprints due to exceptionally high mutation rates.
Electrophoresis 2002;23(4):517-9.
2002: Hoffmann V; Pöhlau D; Przuntek H; Epplen J T; Hardt C
A null mutation within the ciliary neurotrophic factor (CNTF)-gene: implications for susceptibility and disease severity in patients with multiple sclerosis.
Genes and immunity 2002;3(1):53-5.
2002: Klein W; Tromm A; Griga T; Fricke H; Folwaczny C; Hocke M; Eitner K; Marx M; Duerig N; Epplen J T
A polymorphism in the CD14 gene is associated with Crohn disease.
Scandinavian journal of gastroenterology 2002;37(2):189-91.
2002: Kunstmann Erdmute; Hardt Cornelia; Treitz Hartmut; Suerbaum Sebastian; Faller Gerhard; Peitz Ulrich; Schmiegel Wolff; Epplen Jörg T
In the European population HLA-class II genes are not associated with Helicobacter pylori infection.
European journal of gastroenterology & hepatology 2002;14(1):49-53.
2001: Krüger R; Schöls L; Müller T; Kuhn W; Woitalla D; Przuntek H; Epplen J T; Riess O
Evaluation of the gamma-synuclein gene in German Parkinson's disease patients.
Neuroscience letters 2001;310(2-3):191-3.
2001: Klein W; Tromm A; Griga T; Fricke H; Folwaczny C; Hocke M; Eitner K; Marx M; Duerig N; Epplen J T
Interleukin-4 and interleukin-4 receptor gene polymorphisms in inflammatory bowel diseases.
Genes and immunity 2001;2(5):287-9.
2001: Meller S; Jagiello P; Borgmann S; Fricke H; Epplen J T; Gencik M
Novel SNPs in the CD18 gene validate the association with MPO-ANCA+ vasculitis.
Genes and immunity 2001;2(5):269-72.
2001: Holzmann C; Schmidt T; Thiel G; Epplen J T; Riess O
Functional characterization of the human Huntington's disease gene promoter.
Brain research. Molecular brain research 2001;92(1-2):85-97.
2001: Schara U; Gencik M; Mortier J; Langen M; Gencikova A; Epplen J T; Mortier W
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient care.
European journal of pediatrics 2001;160(7):452-3.
2001: Walter C; Gootjes J; Mooijer P A; Portsteffen H; Klein C; Waterham H R; Barth P G; Epplen J T; Kunau W H; Wanders R J; Dodt G
Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.
American journal of human genetics 2001;69(1):35-48.
2001: Mäueler W; Bassili G; Hardt C; Keyl H G; Epplen J T
A complex containing at least one zinc dependent HeLa nuclear protein binds to the intronic (gaa)(n) block of the frataxin gene.
Gene 2001;270(1-2):131-43.
2001: Krüger R; Kuhn W; Leenders K L; Sprengelmeyer R; Müller T; Woitalla D; Portman A T; Maguire R P; Veenma L; Schröder U; Schöls L; Epplen J T; Riess O; Przuntek H
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.
Neurology 2001;56(10):1355-62.
2001: Vorgerd M; Gencik M; Mortier J; Epplen J T; Malin J P; Mortier W
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies.
Muscle & nerve 2001;24(3):421-4.
2001: Klein W; Tromm A; Griga T; Fricke H; Folwaczny C; Hocke M; Eitner K; Marx M; Epplen J T
The polymorphism at position -174 of the IL-6 gene is not associated with inflammatory bowel disease.
European journal of gastroenterology & hepatology 2001;13(1):45-7.
2001: Gencik M; Dahmen N; Wieczorek S; Kasten M; Bierbrauer J; Anghelescu I; Szegedi A; Menezes Saecker A M; Epplen J T
A prepro-orexin gene polymorphism is associated with narcolepsy.
Neurology 2001;56(1):115-7.
2001: Gencik M; Dahmen N; Wieczorek S; Kasten M; Gencikova A; Epplen J T
ApoE polymorphisms in narcolepsy.
BMC medical genetics 2001;2():9.
2000: Klein W; Tromm A; Griga T; Fricke H; Folwaczny C; Hocke M; Eitner K; Marx M; Runte M; Epplen J T
The IL-10 gene is not involved in the predisposition to inflammatory bowel disease.
Electrophoresis 2000;21(17):3578-82.
2000: Kunstmann E; Hardt C; Elitok E; Harder M; Suerbaum S; Peitz U; Schmiegel W; Epplen J T
The nonfunctional allele TCRBV6S1B is strongly associated with Helicobacter pylori infection.
Infection and immunity 2000;68(11):6493-5.
2000: Krüger R; Menezes-Saecker A M; Schöls L; Kuhn W; Müller T; Woitalla D; Berg D; Berger K; Przuntek H; Epplen J T; Riess O
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.
Neuroreport 2000;11(11):2439-42.
2000: Vorgerd M; Schöls L; Hardt C; Ristow M; Epplen J T; Zange J
Mitochondrial impairment of human muscle in Friedreich ataxia in vivo.
Neuromuscular disorders : NMD 2000;10(6):430-5.
2000: Wintermeyer P; Krüger R; Kuhn W; Müller T; Woitalla D; Berg D; Becker G; Leroy E; Polymeropoulos M; Berger K; Przuntek H; Schöls L; Epplen J T; Riess O
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Neuroreport 2000;11(10):2079-82.
2000: Miterski B; Krüger R; Wintermeyer P; Epplen J T
PCR/SSCP detects reliably and efficiently DNA sequence variations in large scale screening projects.
Combinatorial chemistry & high throughput screening 2000;3(3):211-8.
2000: Runte M; Dekomien G; Epplen J T
Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance.
Animal genetics 2000;31(3):223-7.
2000: Dekomien G; Epplen J T
Exclusion of the PDE6A gene for generalised progressive retinal atrophy in 11 breeds of dog.
Animal genetics 2000;31(2):135-9.
2000: Gerken T; Lubjuhn T; Epplen J T
Low probe concentration can cause problems in multilocus DNA fingerprinting (cautionary notes III).
Electrophoresis 2000;21(3):554-5.
2000: Tschentscher F; Kalt A; Hoffmann V; Epplen J; Hardt C
Identification and efficient genotyping of an (A)n/(T)m polymorphism within the 5' untranslated region of the human IL6 gene.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 2000;27(1):1-3.
2000: Gencik M; Gencik A; Mortier W; Epplen J T
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermia.
Human mutation 2000;15(1):122.
2000: Gencik M; Meller S; Borgmann S; Sitter T; Menezes Saecker A M; Fricke H; Epplen J T
The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitides.
Clinical immunology (Orlando, Fla.) 2000;94(1):9-12.
2000: Vandenbroeck K; Hardt C; Louage J; Fiten P; Jäckel S; Ronsse I; Epplen J T; Grimaldi L M; Olsson T; Marrosu M G; Billiau A; Opdenakker G
Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, northern Italy, Sardinia and Sweden.
Genes and immunity 2000;1(4):290-2.
2000: Lamatsch D K; Nanda I; Epplen J T; Schmid M; Schartl M
Unusual triploid males in a microchromosome-carrying clone of the Amazon molly, Poecilia formosa.
Cytogenetics and cell genetics 2000;91(1-4):148-56.
2000: Epplen J T; Gencik M; Epplen A; Andrich J; Saft C; Przuntek H
Morbus Huntington - a human genetic model disease.
Cytogenetics and cell genetics 2000;91(1-4):90-6.
2000: Dekomien G; Runte M; Gödde R; Epplen J T
Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene.
Cytogenetics and cell genetics 2000;90(3-4):261-7.
2000: Krüger R; Hardt C; Tschentscher F; Jäckel S; Kuhn W; Müller T; Werner J; Woitalla D; Berg D; Kühnl N; Fuchs G A; Santos E J; Przuntek H; Epplen J T; Schöls L; Riess O
Genetic analysis of immunomodulating factors in sporadic Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2000;107(5):553-62.
1999: Miterski B; Jaeckel S; Epplen J T; Pöhlau D; Hardt C
The interferon gene cluster: a candidate region for MS predisposition? Multiple Sclerosis Study Group.
Genes and immunity 1999;1(1):37-44.
1999: Goris A; Epplen C; Fiten P; Andersson M; Murru R; Sciacca F L; Ronsse I; Jäckel S; Epplen J T; Marrosu M G; Olsson T; Grimaldi L M; Opdenakker G; Billiau A; Vandenbroeck K
Analysis of an IFN-gamma gene (IFNG) polymorphism in multiple sclerosis in Europe: effect of population structure on association with disease.
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research 1999;19(9):1037-46.
1999: Gencik M; Borgmann S; Zahn R; Albert E; Sitter T; Epplen J T; Fricke H
Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis.
Clinical and experimental immunology 1999;117(2):412-7.
1999: Kunstmann E; Epplen C; Elitok E; Harder M; Suerbaum S; Peitz U; Schmiegel W; Epplen J T
Helicobacter pylori infection and polymorphisms in the tumor necrosis factor region.
Electrophoresis 1999;20(8):1756-61.
1999: Borries C; Launhardt K; Epplen C; Epplen J T; Winkler P
DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys.
Proceedings. Biological sciences / The Royal Society 1999;266(1422):901-4.
1999: Krüger R; Vieira-Saecker A M; Kuhn W; Berg D; Müller T; Kühnl N; Fuchs G A; Storch A; Hungs M; Woitalla D; Przuntek H; Epplen J T; Schöls L; Riess O
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype.
Annals of neurology 1999;45(5):611-7.
1999: Koch R; Scholz M; Nelen M R; Schwechheimer K; Epplen J T; Harders A G
Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literature.
Journal of neurosurgery 1999;90(4):776-9.
1999: Gencik M; Epplen J T; Mortier W
[Diagnosis of neuromuscular diseases: progress with molecular genetic techniques]
Deutsche medizinische Wochenschrift (1946) 1999;124(4):85-7.
1999: Mäueler W; Bassili G; Arnold R; Renkawitz R; Epplen J T
The (gt)n(ga)m containing intron 2 of HLA-DRB alleles binds a zinc-dependent protein and forms non B-DNA structures.
Gene 1999;226(1):9-23.
1999: Mäueler W; Bassili G; Epplen C; Keyl H G; Epplen J T
Protein binding to simple repetitive sequences depends on DNA secondary structure(s).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1999;7(3):163-6.
1999: Krüger R; Vieira-Säcker A M; Kuhn W; Müller T; Woitalla D; Schöls L; Przuntek H; Epplen J T; Riess O
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication.
Journal of neural transmission (Vienna, Austria : 1996) 1999;106(2):159-63.
1998: Peters H C; Kämmer G; Volz A; Kaupmann K; Ziegler A; Bettler B; Epplen J T; Sander T; Riess O
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy.
Neurogenetics 1998;2(1):47-54.
1998: Jaeckel S; Epplen J T; Kauth M; Miterski B; Tschentscher F; Epplen C
Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes.
Electrophoresis 1998;19(18):3055-61.
1998: Holzmann C; Mäueler W; Petersohn D; Schmidt T; Thiel G; Epplen J T; Riess O
Isolation and characterization of the rat huntingtin promoter.
The Biochemical journal 1998;336 ( Pt 1)():227-34.
1998: Schmidt T; Landwehrmeyer G B; Schmitt I; Trottier Y; Auburger G; Laccone F; Klockgether T; Völpel M; Epplen J T; Schöls L; Riess O
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.
Brain pathology (Zurich, Switzerland) 1998;8(4):669-79.
1998: Epplen C; Over I; Lubjuhn T; Epplen J T; Sauer K P
Genetic distinction of scorpionflies (Panorpa vulgaris) by microsatellites.
Molecular ecology 1998;7(9):1256-8.
1998: Klein W; Dekomien G; Holmes N; Epplen J T
Evaluation of ROM1 as a candidate gene in generalised progressive retinal atrophy in dogs.
Animal genetics 1998;29(4):316-8.
1998: Mäueler W; Kyas A; Keyl H G; Epplen J T
A genome-derived (gaa.ttc)24 trinucleotide block binds nuclear protein(s) specifically and forms triple helices.
Gene 1998;215(2):389-403.
1998: Launhardt K; Epplen C; Epplen J T; Winkler P
Amplification of microsatellites adapted from human systems in faecal DNA of wild Hanuman langurs (Presbytis entellus).
Electrophoresis 1998;19(8-9):1356-61.
1998: Schöls L; Krüger R; Amoiridis G; Przuntek H; Epplen J T; Riess O
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Journal of neurology, neurosurgery, and psychiatry 1998;64(1):67-73.
1998: Schlupp I; Nanda I; Döbler M; Lamatsch D K; Epplen J T; Parzefall J; Schmid M; Schartl M
Dispensable and indispensable genes in an ameiotic fish, the Amazon molly Poecilia formosa.
Cytogenetics and cell genetics 1998;80(1-4):193-8.
1998: Epplen J T; Mäueler W; Santos E J
On GATAGATA and other "junk" in the barren stretch of genomic desert.
Cytogenetics and cell genetics 1998;80(1-4):75-82.
1997: Schöls L; Amoiridis G; Przuntek H; Frank G; Epplen J T; Epplen C
Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
Brain : a journal of neurology 1997;120 ( Pt 12)():2131-40.
1997: Schöls L; Amoiridis G; Büttner T; Przuntek H; Epplen J T; Riess O
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
Annals of neurology 1997;42(6):924-32.
1997: Schöls L; Gispert S; Vorgerd M; Menezes Vieira-Saecker A M; Blanke P; Auburger G; Amoiridis G; Meves S; Epplen J T; Przuntek H; Pulst S M; Riess O
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
Archives of neurology 1997;54(9):1073-80.
1997: Epplen C; Santos E J; Mäueler W; van Helden P; Epplen J T
On simple repetitive DNA sequences and complex diseases.
Electrophoresis 1997;18(9):1577-85.
1997: Epplen C; Epplen J T; Frank G; Miterski B; Santos E J; Schöls L
Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene.
Human genetics 1997;99(6):834-6.
1997: Riess O; Laccone F A; Gispert S; Schöls L; Zühlke C; Vieira-Saecker A M; Herlt S; Wessel K; Epplen J T; Weber B H; Kreuz F; Chahrokh-Zadeh S; Meindl A; Lunkes A; Aguiar J; Macek M; Krebsová A; Macek M; Bürk K; Tinschert S; Schreyer I; Pulst S M; Auburger G
SCA2 trinucleotide expansion in German SCA patients.
Neurogenetics 1997;1(1):59-64.
1997: Santos E J; Epplen J T; Epplen C
Extensive gene flow in human populations as revealed by protein and microsatellite DNA markers.
Human heredity 1997;47(3):165-72.
1997: Haupt A; Schöls L; Przuntek H; Epplen J T
Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletions.
Human genetics 1997;99(5):688-91.
1997: Holzmann C; Saecker A M; Epplen J T; Riess O
Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.
Journal of medical genetics 1997;34(3):264.
1997: Epplen C; Jäckel S; Santos E J; D'Souza M; Poehlau D; Dotzauer B; Sindern E; Haupts M; Rüde K P; Weber F; Stöver J; Poser S; Gehler W; Malin J P; Przuntek H; Epplen J T
Genetic predisposition to multiple sclerosis as revealed by immunoprinting.
Annals of neurology 1997;41(3):341-52.
1997: Epplen C; Santos E J; Guerreiro J F; van Helden P; Epplen J T
Coding versus intron variability: extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations.
Human genetics 1997;99(3):399-406.
1997: Schöls L; Riess O; Amoiridis G; Riess A; Przuntek H; Epplen J T
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]
Fortschritte der Neurologie-Psychiatrie 1997;65(2):79-89.
1997: Riess O; Epplen J T; Amoiridis G; Przuntek H; Schöls L
Transmission distortion of the mutant alleles in spinocerebellar ataxia.
Human genetics 1997;99(2):282-4.

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