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Jörg Epplen

Research Profile

Physiology

Genes & Molecular Sequences

Geographic Areas

Germany

Procedures

Concepts & Ideas

Chemicals & Drugs

Phenomena

Polymorphism, Single-Stranded Conformational

Disorders

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Publications

TOP 3
Moritz Lebe; Kirsten Schmieder; Jörg T Epplen; Albrecht Harders; Monika Hasenbring; Sabine Hoffjan; Kathleen Jetschke; Judith Kötting
Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6months after lumbar disc surgery.
Larissa Arning; Jörg T Epplen; Corinna Hendrich; Albert C Ludolph; Elisa Rahikkala; Anne-Dorte Sperfeld
The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.
Sebastian Ocklenburg; Larissa Arning; Jörg T Epplen; Wanda M Gerding; Onur Güntürkün; Christian Beste
Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization.

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2013: Moritz Lebe; Kirsten Schmieder; Jörg T Epplen; Albrecht Harders; Monika Hasenbring; Sabine Hoffjan; Kathleen Jetschke; Judith Kötting
Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6months after lumbar disc surgery.
Pain 2013;154(3):377-84.
2013: Larissa Arning; Jörg T Epplen; Corinna Hendrich; Albert C Ludolph; Elisa Rahikkala; Anne-Dorte Sperfeld
The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.
Neurogenetics 2013;14(1):53-61.
2013: Sebastian Ocklenburg; Larissa Arning; Jörg T Epplen; Wanda M Gerding; Onur Güntürkün; Christian Beste
Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization.
PloS one 2013;8(1):e53643.
2012: Stefanie Schulz; Larissa Arning; Jörg T Epplen; Marlies Pinnow; Christian Beste
N-methyl-D-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test.
Neuropharmacology 2012;63(2):259-65.
2012: Christian Beste; Jörg T Epplen; Vanessa Ness; Ann-Kathrin Stock; Larissa Arning
Differential effects of ADORA2A gene variations in pre-attentive visual sensory memory subprocesses.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2012;22(8):555-61.
2012: Sabine Rudnik-Schöneborn; Larissa Arning; Jörg T Epplen; Klaus Zerres
SETX gene mutation in a family diagnosed autosomal dominant proximal spinal muscular atrophy.
Neuromuscular disorders : NMD 2012;22(3):258-62.
2012: Stefanie Schulz; Edmund Wascher; Larissa Arning; Jörg T Epplen; Marlies Pinnow; Christian Beste
When control fails: influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task.
Neuropharmacology 2012;62(2):1028-33.
2011: Sebastian Ocklenburg; Larissa Arning; Jörg T Epplen; Wanda M Gerding; Onur Güntürkün; Constanze Hahn; Christian Beste
Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization.
Behavioural brain research 2011;225(1):284-9.
2011: Vanessa Ness; Hanna E Niesert; Maik C Stüttgen; Larissa Arning; Jörg T Epplen; Christian Beste
Variations in the GRIN2B gene are associated with risky decision-making.
Neuropharmacology 2011;61(5-6):950-6.
2011: Mine Arslan-Kirchner; Anne De Paepe; Jörg T Epplen; Laurence Faivre; Guillaume Jondeau; Jörg Schmidtke; Bart Loeys
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes.
European journal of human genetics : EJHG 2011;19(10):.
2011: Wanda M Gerding; Saleh Ibrahim; Jan Kremers; Denis A Akkad; Jenny Atorf; Andreia de Castro Marques; Gabriele Dekomien; Rolf Dermietzel; Jörg T Epplen; Andreas Gal; Thomas Rülicke; Sabrina Schreiber; Tobias Schulte-Middelmann; Elisabeth Petrasch-Parwez
Ccdc66 null mutation causes retinal degeneration and dysfunction.
Human molecular genetics 2011;20(18):3620-31.
2011: Andreas M Stadelmann; Georg Juckel; Larissa Arning; Jürgen Gallinat; Jörg T Epplen; Patrik Roser
Association between a cannabinoid receptor gene (CNR1) polymorphism and cannabinoid-induced alterations of the auditory event-related P300 potential.
Neuroscience letters 2011;496(1):60-4.
2011: W M Gerding; S Schreiber; Gabriele Dekomien; Jörg T Epplen
Tracing the origin of 'blue Weimaraner' dogs by molecular genetics.
Journal of animal breeding and genetics = Zeitschrift für Tierzüchtung und Züchtungsbiologie 2011;128(2):153-60.
2011: R Kropatsch; Konrad Streitberger; T Schulte-Middelmann; Gabriele Dekomien; Jörg T Epplen
On ancestors of dog breeds with focus on Weimaraner hunting dogs.
Journal of animal breeding and genetics = Zeitschrift für Tierzüchtung und Züchtungsbiologie 2011;128(1):64-72.
2011: Christian Beste; Daniel Schneider; Jörg T Epplen; Larissa Arning
The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processes.
Neuropharmacology 2011;60(2-3):467-71.
2011: Carsten Saft; Sarah J Tabrizi; Stefan Wieczorek; Justo Garcia de Yebenes; David Craufurd; Matthias Dose; Jörg T Epplen; G Bernhard Landwehrmeyer; Raymund A C Roos; Larissa Arning
NMDA receptor gene variations as modifiers in Huntington disease: a replication study.
PLoS currents 2011;3():RRN1247.
2011: Dunja K Lamatsch; Michael Schmid; S Schories; V Trifonov; Jörg T Epplen; Manfred Schartl
Isolation of a cancer-associated microchromosome in the sperm-dependent parthenogen Poecilia formosa.
Cytogenetic and genome research 2011;135(2):135-42.
2011: Elahe Taherzadeh-Fard; Stefan Wieczorek; Denis A Akkad; Andrew Chan; Jörg T Epplen; Aiden Haghikia; Carsten Saft; Larissa Arning
PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease.
Molecular neurodegeneration 2011;6(1):32.
2010: A Gäckler; A K Eickelmann; Dominik Brors; Stefan Dazert; Jörg T Epplen; Erdmute Kunstmann
Positive family history of idiopathic sudden sensorineural hearing loss.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2010;267(12):1843-8.
2010: Elahe Taherzadeh-Fard; Carsten Saft; Stefan Wieczorek; Jörg T Epplen; Larissa Arning
Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1.
Neurogenetics 2010;11(4):435-9.
2010: Kathrin Wessels; Bettina Bohnhorst; Ingrid Luhmer; Susanne Morlot; Axel Bohring; Jon Jonasson; Jörg T Epplen; Dorothea Gadzicki; Stefanie Glaser; Gudrun Göhring; Madeleine Mälzer; Anke Hein; Mine Arslan-Kirchner; Manfred Stuhrmann; Jörg Schmidtke; Brigitte Pabst
Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome.
European journal of medical genetics 2010;53(5):280-5.
2010: Gabriele Dekomien; Conni Vollrath; Elisabeth Petrasch-Parwez; Michael H Boevé; Denis A Akkad; Wanda M Gerding; Jörg T Epplen
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.
Neurogenetics 2010;11(2):163-74.
2010: Stefan Wieczorek; Julia U Holle; Stephanie Müller; Harald Fricke; Wolfgang L Gross; Jörg T Epplen
A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener's granulomatosis.
Journal of molecular medicine (Berlin, Germany) 2010;88(4):413-21.
2010: Christiane Schneider-Gold; Judith Kötting; Jörg T Epplen; Ralf Gold; Wanda M Gerding
Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero.
Muscle & nerve 2010;41(4):550-4.
2010: Jürgen Glas; Julia Seiderer; Melinda Nagy; Christoph Fries; Florian Beigel; Maria Weidinger; Simone Pfennig; Wolfram Klein; Jörg T Epplen; Peter Lohse; Matthias Folwaczny; Burkhard Göke; Thomas Ochsenkühn; Julia Diegelmann; Bertram Müller-Myhsok; Darina Roeske; Stephan Brand
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
PloS one 2010;5(4):e10373.
2010: Stefan Wieczorek; Julia U Holle; Jörg T Epplen
Recent progress in the genetics of Wegener's granulomatosis and Churg-Strauss syndrome.
Current opinion in rheumatology 2010;22(1):8-14.
2009: Stefan Wieczorek; Sabine Hoffjan; A Chan; L Rey; L Harper; Harald Fricke; J U Holle; Wolfgang L Gross; Jörg T Epplen; Peter Lamprecht
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: Xinhua Yu; S Wieczorek; Andre Franke; H Yin; M Pierer; C Sina; T H Karlsen; K M Boberg; A Bergquist; M Kunz; T Witte; W L Gross; Jörg T Epplen; M E Alarcón-Riquelme; Stefan Schreiber; Saleh M Ibrahim
Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases.
Genes and immunity 2009;10(6):601-5.
2009: Susanne Stemmler; Michael Nothnagel; Qumar Parwez; Elisabeth Petrasch-Parwez; Jörg T Epplen; Sabine Hoffjan
Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.
International journal of immunogenetics 2009;36(4):217-22.
2009: Jürgen Glas; Johannes Stallhofer; Stephan Ripke; Martin Wetzke; Simone Pfennig; Wolfram Klein; Jörg T Epplen; Thomas Griga; Uwe Schiemann; Martin Lacher; Sibylle Koletzko; Matthias Folwaczny; Peter Lohse; Burkhard Göke; Thomas Ochsenkühn; Bertram Müller-Myhsok; Stephan Brand
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: Peter Lamprecht; Stefan Wieczorek; Jörg T Epplen; Petra Ambrosch; Cees G M Kallenberg
Granuloma formation in ANCA-associated vasculitides.
APMIS. Supplementum 2009;(127):32-6.
2009: Jürgen Glas; Julia Seiderer; Giulia Pasciuto; Cornelia Tillack; Julia Diegelmann; Simone Pfennig; Astrid Konrad; Silke Schmechel; Martin Wetzke; Helga-Paula Török; Johannes Stallhofer; Matthias Jürgens; Thomas Griga; Wolfram Klein; Jörg T Epplen; Uwe Schiemann; Thomas Mussack; Peter Lohse; Burkhard Göke; Thomas Ochsenkühn; Matthias Folwaczny; Bertram Müller-Myhsok; Stephan Brand
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: Denis A Akkad; Sabine Hoffjan; Elisabeth Petrasch-Parwez; J Beygo; Ralf Gold; Jörg T Epplen
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients.
Journal of autoimmunity 2009;32(2):110-5.
2009: Jasmin Beygo; Qumar Parwez; Elisabeth Petrasch-Parwez; Jörg T Epplen; Sabine Hoffjan
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: Stefan Wieczorek; Silvia Knaup; Wolfgang L Gross; Jörg T Epplen
Genetic variability of RXRB, PPARA, and PPARG in Wegener's granulomatosis.
PPAR research 2009;2009():786781.
2009: Umut Arinir; Sabine Hoffjan; H Knoop; Gerhard Schultze-Werninghaus; Jörg T Epplen; Gernot Rohde
[The genetics of chronic obstructive pulmonary disease].
Pneumologie (Stuttgart, Germany) 2009;63(1):41-8.
2008: Lars Klinge; Gabriele Dekomien; Ahmed Aboumousa; Richard Charlton; Jörg T Epplen; Rita Barresi; Kate Bushby; Volker Straub
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?
Neuromuscular disorders : NMD 2008;18(12):934-41.
2008: Larissa Arning; Ludger Schöls; Huriye Cin; Manfred Souquet; Jörg T Epplen; Dagmar Timmann
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: M Heckmann; J U Holle; Larissa Arning; S Knaup; Bernhard Hellmich; Michael Nothnagel; Peter Jagiello; Wolfgang L Gross; Jörg T Epplen; Stefan Wieczorek
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: Stefan Wieczorek; Bernhard Hellmich; Larissa Arning; Frank Moosig; Peter Lamprecht; Wolfgang L Gross; Jörg T Epplen
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: Ludger Schöls; Larissa Arning; Rebecca Schüle; Jörg T Epplen; Dagmar Timmann
"Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2).
Journal of neurology 2008;255(4):495-501.
2008: Larissa Arning; didier monte; Wiebke Hansen; Stefan Wieczorek; Peter Jagiello; Denis A Akkad; Jürgen Andrich; Peter H Kraus; Carsten Saft; Jörg T Epplen
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: Oliver Adrian; Sylvia Kaiser; Norbert Sachser; Pia Jandewerth; Petra Löttker; Jörg T Epplen; Michael B Hennessy
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: Jürgen Glas; Astrid Konrad; Silke Schmechel; Julia Dambacher; Julia Seiderer; Frieder Schroff; Martin Wetzke; Darina Roeske; Helga-Paula Török; Laurian Tonenchi; Simone Pfennig; Dirk Haller; Thomas Griga; Wolfram Klein; Jörg T Epplen; Christian Folwaczny; Peter Lohse; Burkhard Göke; Thomas Ochsenkühn; Thomas Mussack; Matthias Folwaczny; Bertram Müller-Myhsok; Stephan Brand
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: Christoph Münch; Jörg T Epplen; Moritz Meins; Robert Meyer; Jörg R Weber; Thomas Meyer
Severe Guillain-Barré syndrome associated with chromosome 17p11.2-12 duplication.
Muscle & nerve 2008;37(2):256-8.
2008: Jan Börgel; Daniel Bulut; Christoph Hanefeld; Horst Neubauer; Andreas Mügge; Jörg T Epplen; Tim Holland-Letz; Martin Spiecker
The CYP2J2 G-50T polymorphism and myocardial infarction in patients with cardiovascular risk profile.
BMC cardiovascular disorders 2008;8():41.
2008: Denis A Akkad; Niels Kruse; Larissa Arning; Ralf Gold; Jörg T Epplen
Genomic NGFB variation and multiple sclerosis in a case control study.
BMC medical genetics 2008;9():107.
2008: Qumar Parwez; Susanne Stemmler; Jörg T Epplen; Sabine Hoffjan
Variation in genes encoding eosinophil granule proteins in atopic dermatitis patients from Germany.
Journal of negative results in biomedicine 2008;7():9.
2008: Katharina J Schlang; Larissa Arning; Jörg T Epplen; Susanne Stemmler
Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).
BMC medical genetics 2008;9():71.
2007: Denis A Akkad; Larissa Arning; S M Ibrahim; Jörg T Epplen
Sex specifically associated promoter polymorphism in multiple sclerosis affects interleukin 4 expression levels.
Genes and immunity 2007;8(8):703-6.
2007: Kathrin P Lampert; Dunja K Lamatsch; Petra Fischer; Jörg T Epplen; Indrajit Nanda; Michael Schmid; Manfred Schartl
Automictic reproduction in interspecific hybrids of poeciliid fish.
Current biology : CB 2007;17(22):1948-53.
2007: Karel Janko; Jörg Bohlen; Dunja Lamatsch; Martin Flajshans; Jörg T Epplen; Petr Ráb; Petr Kotlík; Vendula Slechtová
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: Larissa Arning; Carsten Saft; Stefan Wieczorek; Jürgen Andrich; Peter H Kraus; Jörg T Epplen
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: Wanda M Blaszczyk; Claudia Distler; Gabriele Dekomien; Larissa Arning; Klaus-Peter Hoffmann; Jörg T Epplen
Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo).
Animal genetics 2007;38(4):421-3.
2007: Filippina Macaluso; Michael Nothnagel; Qumar Parwez; Elisabeth Petrasch-Parwez; Falk G Bechara; Jörg T Epplen; Sabine Hoffjan
Polymorphisms in NACHT-LRR (NLR) genes in atopic dermatitis.
Experimental dermatology 2007;16(8):692-8.
2007: Tim Schmoll; F M Schurr; Wolfgang Winkel; Jörg T Epplen; Thomas Lubjuhn
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: Jürgen Glas; Helga-Paula Török; Laurian Tonenchi; Martin Wetzke; Vanessa Beynon; Molla Y Teshome; Sebastian Cotofana; Uwe Schiemann; Thomas Griga; Wolfram Klein; Jörg T Epplen; Christian Folwaczny; Matthias Folwaczny; Thomas Mussack; Elisabeth H Weiss
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: Oliver Vonend; Christian Altenhenne; Nikolaus Büchner; Gabriele Dekomien; Christiane Maser-Gluth; Stefan M Weiner; Lorenz Sellin; Stefan Hofebauer; Jörg T Epplen; Lars Christian Rump
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: Susanne Stemmler; Qumar Parwez; Elisabeth Petrasch-Parwez; Jörg T Epplen; Sabine Hoffjan
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: Jürgen Glas; Julia Seiderer; Martin Wetzke; Astrid Konrad; Helga-Paula Török; Silke Schmechel; Laurian Tonenchi; Christine Grassl; Julia Dambacher; Simone Pfennig; Kerstin Maier; Thomas Griga; Wolfram Klein; Jörg T Epplen; Uwe Schiemann; Christian Folwaczny; Peter Lohse; Burkhard Göke; Thomas Ochsenkühn; Bertram Müller-Myhsok; Matthias Folwaczny; Thomas Mussack; Stephan Brand
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: Tobias T Schimming; Qumar Parwez; Elisabeth Petrasch-Parwez; Michael Nothnagel; Jörg T Epplen; Sabine Hoffjan
Association of toll-interacting protein gene polymorphisms with atopic dermatitis.
BMC dermatology 2007;7():3.
2007: Nina K Bartels; Jan Börgel; Stefan Wieczorek; Nikolaus Büchner; Christoph Hanefeld; Daniel Bulut; Andreas Mügge; Lars Christian Rump; Bernd M Sanner; Jörg T Epplen
Risk factors and myocardial infarction in patients with obstructive sleep apnea: impact of beta2-adrenergic receptor polymorphisms.
BMC medicine 2007;5():1.
2006: Sabine Hoffjan; Qumar Parwez; Elisabeth Petrasch-Parwez; D Falkenstein; Michael Nothnagel; Jörg T Epplen
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: Sabine Hoffjan; Charlotte Thiels; Matthias Vorgerd; Eva Neuen-Jacob; Jörg T Epplen; Wolfram Kress
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: Denis A Akkad; René Gödde; Jörg T Epplen
No association between synapsin III gene promoter polymorphisms and multiple sclerosis in German patients.
Journal of neurology 2006;253(10):1365-6.
2006: Oliver Rommel; Rudolf A Kley; Gabriele Dekomien; Jörg T Epplen; Matthias Vorgerd; Monika Hasenbring
Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related coping.
Pain 2006;124(3):295-304.
2006: K Bach; J Preyer; A Jensen; Jörg T Epplen; Erdmute Kunstmann
[Gynecological outpatient management in HNPCC].
Zentralblatt für Gynäkologie 2006;128(4):207-12.
2006: Jürgen Glas; Helga-Paula Török; Laurian Tonenchi; Bertram Müller-Myhsok; Thomas Mussack; Martin Wetzke; Wolfram Klein; Jörg T Epplen; Thomas Griga; Uwe Schiemann; Peter Lohse; Julia Seiderer; Fabian Schnitzler; Stephan Brand; Thomas Ochsenkühn; Matthias Folwaczny; Christian Folwaczny
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: Anna Melissa Schlitter; D Woitalla; T Mueller; Jörg T Epplen; Gabriele Dekomien
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: Katrin Zunker; Jörg T Epplen; Manfred Schartl
Genomic stability in malignant melanoma of Xiphophorus.
Melanoma research 2006;16(2):105-13.
2006: Peter Felderbauer; Wolfram Klein; Kerem Bulut; Nikolaus Ansorge; Gabriele Dekomien; I Werner; Jörg T Epplen; Frank Schmitz; Wolfgang E Schmidt
Mutations in the calcium-sensing receptor: a new genetic risk factor for chronic pancreatitis?
Scandinavian journal of gastroenterology 2006;41(3):343-8.
2006: René Gödde; Denis A Akkad; Larissa Arning; Gabriele Dekomien; Julia Herchenbach; Erdmute Kunstmann; Moritz Meins; Stefan Wieczorek; Jörg T Epplen; Sabine Hoffjan
Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.
Electrophoresis 2006;27(5-6):939-46.
2006: Denis A Akkad; Peter Jagiello; P Szyld; R Goedde; Stefan Wieczorek; Wolfgang L Gross; Jörg T Epplen
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: Annegret Müller; Hans K Schackert; Bettina Lange; Josef Rüschoff; Laslow Füzesi; Joerg Willert; Peter Burfeind; Parantu Shah; Heinz Becker; Jörg T Epplen; Susanne Stemmler
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: Maren Mai; Amer D Akkad; Stefan Wieczorek; Carsten Saft; Jürgen Andrich; Peter H Kraus; Jörg T Epplen; Larissa Arning
No association between polymorphisms in the BDNF gene and age at onset in Huntington disease.
BMC medical genetics 2006;7():79.
2006: Kathrin Engelfried; Matthias Vorgerd; Michaela Hagedorn; Gerhard Haas; Jürgen Gilles; Jörg T Epplen; Moritz Meins
Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).
BMC medical genetics 2006;7():53.
2006: Paweł Szyld; Peter Jagiello; Elena Csernok; Wolfgang L Gross; Jörg T Epplen
On the Wegener granulomatosis associated region on chromosome 6p21.3.
BMC medical genetics 2006;7():21.
2006: Stefan Wieczorek; Larissa Arning; Ingrid Alheite; Jörg T Epplen
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: Anna Melissa Schlitter; M Kurz; Jan Petter Larsen; Dirk Woitalla; Thomas Müller; Jörg T Epplen; Gabriele Dekomien
Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts.
Acta neurologica Scandinavica 2006;113(1):9-13.
2006: Jan Börgel; Tino Schulz; Nina K Bartels; Jörg T Epplen; Nikolaus Büchner; Lars Christian Rump; Anika Huesing; Bernd M Sanner; Andreas Mügge
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: Reiner Sprengelmeyer; Ulrike Schroeder; Andy Young; Jörg T Epplen
Disgust in pre-clinical Huntington's disease: a longitudinal study.
Neuropsychologia 2006;44(4):518-33.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):543.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):543.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):542.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):541-2.
2005: Gabriele Dekomien; Martin Gencik; Alexandra Gencikova; Yvonne Klenk; Jörg T Epplen
Gene symbol: RYR1. Disease: malignant hyperthermia.
Human genetics 2005;118(3-4):541.
2005: Peter Jagiello; Peer M Aries; Larissa Arning; Sonja E N Wagenleiter; Elena Csernok; Bernhard Hellmich; Wolfgang L Gross; Jörg T Epplen
The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.
Arthritis and rheumatism 2005;52(12):4039-43.
2005: Elisabeth Petrasch-Parwez; Carsten Saft; Annegrit Schlichting; Jürgen Andrich; Markus Napirei; Larissa Arning; Stefan Wieczorek; Rolf Dermietzel; Jörg T Epplen
Is the retina affected in Huntington disease?
Acta neuropathologica 2005;110(5):523-5.
2005: Larissa Arning; Peter H Kraus; Carsten Saft; Jürgen Andrich; Jörg T Epplen
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: Sonja E N Wagenleiter; Wolfram Klein; Thomas Griga; W Schmiegel; Jörg T Epplen; Peter Jagiello
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: Susanne Vogler; René Goedde; Bianca Miterski; Ralf Gold; Antje Kroner; Dirk Koczan; Uwe K Zettl; Peter Rieckmann; Jörg T Epplen; Saleh M Ibrahim
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: Helga-Paula Török; Jürgen Glas; Laurian Tonenchi; Peter Lohse; Bertram Müller-Myhsok; Olga Limbersky; C Neugebauer; Fabian Schnitzler; Julia Seiderer; Cornelia Tillack; Stephan Brand; Günter Brünnler; Peter Jagiello; Jörg T Epplen; Thomas Griga; Wolfram Klein; Uwe Schiemann; Matthias Folwaczny; Thomas Ochsenkühn; Christian Folwaczny
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.
Gut 2005;54(10):1421-7.
2005: Sabine Hoffjan; Susanne Stemmler; Qumar Parwez; Elisabeth Petrasch-Parwez; Umut Arinir; Gernot Rohde; Karin Reinitz-Rademacher; Gerhard Schultze-Werninghaus; Albrecht Bufe; Jörg T Epplen
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: Burkhard Alber; Magdalena Pernauer; Annemarie Schwan; Gabriele Rothmund; Karl T Hoffmann; Dagmar Brummer; Anne-Dorte Sperfeld; Ingo Uttner; Heinrich Binder; Jörg T Epplen; Jörn Dullinger; Albert C Ludolph; Thomas Meyer
Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.
Journal of the neurological sciences 2005;236(1-2):9-12.
2005: Sabine Hoffjan; Jörg T Epplen
The genetics of atopic dermatitis: recent findings and future options.
Journal of molecular medicine (Berlin, Germany) 2005;83(9):682-92.
2005: Erdmute Kunstmann; A Hildmann; Jürgen Lautermann; Christoph Aletsee; Jörg T Epplen; Holger Sudhoff
[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].
HNO 2005;53(9):773-8.
2005: Umut Arinir; Wolfram Klein; Gernot Rohde; Susanne Stemmler; Jörg T Epplen; Gerhard Schultze-Werninghaus
Polymorphisms in the interleukin-8 gene in patients with chronic obstructive pulmonary disease.
Electrophoresis 2005;26(15):2888-91.
2005: K Bach; D Hüppe; Wolff Schmiegel; Jörg T Epplen; Erdmute Kunstmann
[Evaluation of outpatient management in HNPCC].
Zeitschrift für Gastroenterologie 2005;43(7):647-51.
2005: René Gödde; Klaus Rohde; Christian Becker; Mahammad R Toliat; Patricia Entz; Anita Suk; Norbert Müller; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Peter Nürnberg; Jörg T Epplen
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: Thomas Griga; C Wilkens; Wolff Schmiegel; Christian Folwaczny; M Hagedorn; Natascha Duerig; Jörg T Epplen; Wolfram Klein
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: Stefan Wieczorek; Jörg T Epplen
Gene symbol: PANK2. Disease: Pantothenate kinase associated neurodegeneration (PKAN).
Human genetics 2005;116(6):545.
2005: Stefan Wieczorek; Jörg T Epplen
Gene symbol: PANK2. Disease: Pantothenate kinase associated neurodegeneration (PKAN).
Human genetics 2005;116(6):535.
2005: Tanja Schrameyer; Gabriele Dekomien; Sandra M Pasternack; Benedikt S Reinartz; Eduardo J M Santos; Jörg T Epplen
Long- and short-haired Weimaraner dogs represent two populations of one breed.
Electrophoresis 2005;26(9):1668-72.
2005: Susanne Stemmler; Umut Arinir; Wolfram Klein; Gernot Rohde; Sabine Hoffjan; N Wirkus; Karin Reinitz-Rademacher; Albrecht Bufe; Gerhard Schultze-Werninghaus; Jörg T Epplen
Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.
Genes and immunity 2005;6(3):225-30.
2005: Kathrin P Lampert; Dunja K Lamatsch; Jörg T Epplen; Manfred Schartl
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: Wanda M Blaszczyk; Larissa Arning; Klaus-Peter Hoffmann; Jörg T Epplen
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: Wolfram Klein; Andreas Tromm; Christian Folwaczny; Michaela Hagedorn; Natascha Duerig; Jörg T Epplen; Wolff Schmiegel; Thomas Griga
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: Tim Schmoll; Verena Dietrich; Wolfgang Winkel; Jörg T Epplen; Frank Schurr; Thomas Lubjuhn
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: Larissa Arning; Peter H Kraus; Sandra Valentin; Carsten Saft; Jürgen Andrich; Jörg T Epplen
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease.
Neurogenetics 2005;6(1):25-8.
2005: Moritz Meins; J Lehmann; F Gerresheim; Julia Herchenbach; M Hagedorn; K Hameister; Jörg T Epplen
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: Peter Jagiello; Wolfram Klein; H Schultz; Elena Csernok; Wolfgang L Gross; Jörg T Epplen
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: Wiebke Hansen; Carsten Saft; Jürgen Andrich; Thomas Müller; Stefan Wieczorek; Jörg T Epplen; Larissa Arning
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: Anna Melissa Schlitter; Martin Kurz; Jan Petter Larsen; Dirk Woitalla; Thomas Mueller; Jörg T Epplen; Gabriele Dekomien
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: Sonja E N Wagenleiter; Peter Jagiello; Denis A Akkad; Larissa Arning; Thomas Griga; Wolfram Klein; Jörg T Epplen
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: René Gödde; Stefanie Brune; Peter Jagiello; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Norbert Müller; Jörg T Epplen
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: Peter Jagiello; Stefan Wieczorek; Philipp Yu; Elena Csernok; Wolfgang L Gross; Jörg T Epplen
Association study with Wegener granulomatosis of the human phospholipase Cgamma2 gene.
Journal of negative results in biomedicine 2005;4():1.
2005: Peter Felderbauer; Peter Hoffmann; Wolfram Klein; Kerem Bulut; Nikolaus Ansorge; Jörg T Epplen; Frank Schmitz; Wolfgang E Schmidt
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: Peter Jagiello; Wolfgang L Gross; Jörg T Epplen
Complex genetics of Wegener granulomatosis.
Autoimmunity reviews 2005;4(1):42-7.
2005: Moritz Meins; Javad Karimzad Hagh; Fritz Gerresheim; Elisabeth Einhoff; Heidi Olschewski; Henning Strehl; Jörg T Epplen
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.
2004: Pablo Serrano-Fernández; Saleh M Ibrahim; Uwe K Zettl; Hans-Jürgen Thiesen; R Gödde; Jörg T Epplen; Steffen Möller
Intergenomic consensus in multifactorial inheritance loci: the case of multiple sclerosis.
Genes and immunity 2004;5(8):615-20.
2004: Carsten Saft; Jürgen Andrich; Nils Brune; Martin Gencik; Peter H Kraus; Horst Przuntek; Jörg T Epplen
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: Elisabeth Petrasch-Parwez; Hans-Werner Habbes; Svenja Weickert; Marlen Löbbecke-Schumacher; Katharine Striedinger; Stefan Wieczorek; Rolf Dermietzel; Jörg T Epplen
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: Stefan Wieczorek; Peter Jagiello; Larissa Arning; Norbert Dahmen; Jörg T Epplen
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: René Gödde; Viktoria Nigmatova; Peter Jagiello; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Jörg T Epplen
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: Erdmute Kunstmann; Judith Vieland; Frank Brasch; Stephan Hahn; Jörg T Epplen; Karsten Schulmann; Wolff Schmiegel
HNPCC: six new pathogenic mutations.
BMC medical genetics 2004;5():16.
2004: Maggie C Walter; G Dekomien; Beate Schlotter-Weigel; Peter Reilich; Dieter Pongratz; Wolfgang Müller-Felber; Jörg T Epplen; Angela Huebner; Hanns Lochmüller
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: Peter Jagiello; Martin Gencik; Larissa Arning; Stefan Wieczorek; Erdmute Kunstmann; Elena Csernok; Wolfgang L Gross; Jörg T Epplen
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: Larissa Arning; Peter Jagiello; Stefan Wieczorek; Carsten Saft; Jürgen Andrich; Jörg T Epplen
Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease.
BMC medical genetics 2004;5():7.
2004: Stefan Wieczorek; Norbert Dahmen; Meike Kasten; Jörg T Epplen; Martin Gencik
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: Wolfram Klein; Gernot Rohde; Umut Arinir; Michaela Hagedorn; Natascha Dürig; Gerhard Schultze-Werninghaus; Jörg T Epplen
A promotor polymorphism in the Interleukin 11 gene is associated with chronic obstructive pulmonary disease.
Electrophoresis 2004;25(6):804-8.
2004: Wolfram Klein; Andreas Tromm; Christian Folwaczny; Michaela Hagedorn; Natascha Duerig; Jörg T Epplen; Wolff Schmiegel; Thomas Griga
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: Bianca Miterski; Susanne Drynda; Gundula Böschow; Wolfram Klein; Joachim Oppermann; Jörn Kekow; Jörg T Epplen
Complex genetic predisposition in adult and juvenile rheumatoid arthritis.
BMC genetics 2004;5():2.
2004: Nils Brune; Jürgen Andrich; Martin Gencik; Carsten Saft; Thomas Müller; S Valentin; Horst Przuntek; Jörg T Epplen
Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's disease.
Journal of neural transmission. Supplementum 2004;(68):105-10.
2004: Dunja K Lamatsch; Indrajit Nanda; Ingo Schlupp; Jörg T Epplen; Michael Schmid; Manfred Schartl
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.
2004: Larissa Arning; Peter Jagiello; Ulrike Schara; Matthias Vorgerd; Norbert Dahmen; Alexandra Gencikova; Wilhelm Mortier; Jörg T Epplen; Martin Gencik
Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.
Journal of neurology 2004;251(1):72-8.
2003: Rejko Krüger; Christian Fischer; Thorsten Schulte; Karsten M Strauss; Thomas Müller; Dirk Woitalla; Daniela Berg; Marcel Hungs; René Gobbele; Klaus Berger; Jörg T Epplen; Olaf Riess; Ludger Schöls
Mutation analysis of the neurofilament M gene in Parkinson's disease.
Neuroscience letters 2003;351(2):125-9.
2003: Gabriele Dekomien; Jörg T Epplen
Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy.
Molecular vision 2003;9():601-5.
2003: Wolfram Klein; Andreas Tromm; Thomas Griga; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; Natascha Duerig; Jörg T Epplen
Interaction of polymorphisms in the CARD15 and CD14 genes in patients with Crohn disease.
Scandinavian journal of gastroenterology 2003;38(8):834-6.
2003: Tim Schmoll; Volker Janzon; Jörg T Epplen; Thomas Lubjuhn
Extra-pair sires as identified by means of standardized across-gel comparisons of multilocus DNA fingerprints.
Electrophoresis 2003;24(16):2758-63.
2003: Stefan Boehringer; Cornelia Hardt; Bianca Miterski; Ansgar Steland; Jörg T Epplen
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: Frank Rutsch; Nico Ruf; Sucheta M Vaingankar; Mohammad R Toliat; Anita Suk; Wolfgang Höhne; Galen Schauer; Mandy Lehmann; Tony Roscioli; Dirk Schnabel; Jörg T Epplen; Alex Knisely; andrea superti-furga; James McGill; Marco Filippone; Alan R Sinaiko; Hillary Vallance; Bernd Hinrichs; Wendy Smith; Merry Ferre; Robert Terkeltaub; Peter Nürnberg
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification.
Nature genetics 2003;34(4):379-81.
2003: Gabriele Dekomien; Jörg T Epplen
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: T Schulte; Stefan Boehringer; Ludger Schöls; Thomas Müller; C Fischer; Olaf Riess; Horst Przuntek; K Berger; Jörg T Epplen; Rejko Krüger
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: Stefan Wieczorek; Martin Gencik; Dan Rujescu; Peter Tonn; Ina Giegling; Jörg T Epplen; Norbert Dahmen
TNFA promoter polymorphisms and narcolepsy.
Tissue antigens 2003;61(6):437-42.
2003: Peter Jagiello; C Hammans; Stefan Wieczorek; Larissa Arning; A Stefanski; Henning Strehl; Jörg T Epplen; Martin Gencik
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: T Schulte; Bianca Miterski; Christian Börnke; Horst Przuntek; Jörg T Epplen; Ludger Schöls
Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia.
Neurology 2003;60(9):1529-32.
2003: Tim Schmoll; Verena Dietrich; Wolfgang Winkel; Jörg T Epplen; Thomas Lubjuhn
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: Erdmute Kunstmann; Cornelia Hardt; Jean E Crabtree; Sebastian Suerbaum; Jörg T Epplen
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: Stefan Wieczorek; Norbert Dahmen; Peter Jagiello; Jörg T Epplen; Martin Gencik
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: Norbert Dahmen; Meike Kasten; Stefan Wieczorek; Martin Gencik; Jörg T Epplen; B Ullrich
Increased frequency of migraine in narcoleptic patients: a confirmatory study.
Cephalalgia : an international journal of headache 2003;23(1):14-9.
2002: Wolfram Klein; Andreas Tromm; Thomas Griga; Harald Fricke; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; Natascha Duerig; Jörg T Epplen
A polymorphism in the IL11 gene is associated with ulcerative colitis.
Genes and immunity 2002;3(8):494-6.
2002: Gabriele Dekomien; Jörg T Epplen
The canine Recoverin (RCV1) gene: a candidate gene for generalized progressive retinal atrophy.
Molecular vision 2002;8():436-41.
2002: Carsten Hohoff; Katrin Solmsdorff; Petra Löttker; Kristina Kemme; Jörg T Epplen; Trevor G Cooper; Norbert Sachser
Monogamy in a new species of wild guinea pigs (Galea sp.).
Die Naturwissenschaften 2002;89(10):462-5.
2002: Rene Goedde; Stephen Sawcer; Stefan Boehringer; Bianca Miterski; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Alastair Compston; Jörg T Epplen
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: P Wintermeyer; Olaf Riess; Ludger Schöls; Horst Przuntek; Bianca Miterski; Jörg T Epplen; Rejko Krüger
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: Simone M Sauter; Bianca Miterski; Sven Klimpe; D Bönsch; Ludger Schöls; A Visbeck; T Papke; H C Hopf; Wolfgang Engel; Thomas Deufel; Jörg T Epplen; Juergen Neesen
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: Gabriele Dekomien; Jörg T Epplen
Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy.
BMC genetics 2002;3():12.
2002: Gabriele Dekomien; Jörg T Epplen
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: Bianca Miterski; Stefan Boehringer; Wolfram Klein; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Jörg T Epplen
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: Jürgen Andrich; T Schmitz; Carsten Saft; Thomas Postert; Peter H Kraus; Jörg T Epplen; Horst Przuntek; Marcus W Agelink
Autonomic nervous system function in Huntington's disease.
Journal of neurology, neurosurgery, and psychiatry 2002;72(6):726-31.
2002: Bianca Miterski; Eckhart Sindern; Michael Haupts; Sebastian Schimrigk; Jörg T Epplen
PTPRC (CD45) is not associated with multiple sclerosis in a large cohort of German patients.
BMC medical genetics 2002;3():3.
2002: Ingrid Bauer; Martin Gencik; Franco Laccone; Hartmut Peters; Bernhard H F Weber; Elke Holinski Feder; Helga Weirich; Deborah J Morris-Rosendahl; Arndt Rolfs; Alexandra Gencikova; Peter Bauer; Gregor Wenning; Jörg T Epplen; Susan E Holmes; Russell L Margolis; Christopher A Ross; Olaf Riess
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: Bianca Miterski; Jörg T Epplen; Martin Gencik
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: Martin Gencik; C Hammans; Henning Strehl; N Wagner; Jörg T Epplen
Chorea Huntington: a rare case with childhood onset.
Neuropediatrics 2002;33(2):90-2.
2002: Matthias Stöck; Dunja K Lamatsch; Claus Steinlein; Jörg T Epplen; Wolf-Rüdiger Grosse; Robert Hock; Thomas Klapperstück; Kathrin P Lampert; Ulrich Scheer; Michael Schmid; Manfred Schartl
A bisexually reproducing all-triploid vertebrate.
Nature genetics 2002;30(3):325-8.
2002: Thomas Lubjuhn; Anna Sramkova; Juan F Masello; Petra Quillfeldt; Jörg T Epplen
Truly hypervariable DNA fingerprints due to exceptionally high mutation rates.
Electrophoresis 2002;23(4):517-9.
2002: Volker Hoffmann; Dieter Pöhlau; Horst Przuntek; Jörg T Epplen; Cornelia Hardt
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: Wolfram Klein; Andreas Tromm; Thomas Griga; Harald Fricke; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; Natascha Duerig; Jörg T Epplen
A polymorphism in the CD14 gene is associated with Crohn disease.
Scandinavian journal of gastroenterology 2002;37(2):189-91.
2002: Erdmute Kunstmann; Cornelia Hardt; Hartmut Treitz; Sebastian Suerbaum; Gerhard Faller; Ulrich Peitz; Wolff Schmiegel; Jörg T Epplen
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: Rejko Krüger; Ludger Schöls; Thomas Müller; Wilfried Kuhn; Dirk Woitalla; Horst Przuntek; Jörg T Epplen; Olaf Riess
Evaluation of the gamma-synuclein gene in German Parkinson's disease patients.
Neuroscience letters 2001;310(2-3):191-3.
2001: Carsten Holzmann; Thorsten Schmidt; G Thiel; Jörg T Epplen; Olaf Riess
Functional characterization of the human Huntington's disease gene promoter.
Brain research. Molecular brain research 2001;92(1-2):85-97.
2001: Wolfram Klein; Andreas Tromm; Thomas Griga; Harald Fricke; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; Natascha Duerig; Jörg T Epplen
Interleukin-4 and interleukin-4 receptor gene polymorphisms in inflammatory bowel diseases.
Genes and immunity 2001;2(5):287-9.
2001: S Meller; Peter Jagiello; Stefan Borgmann; Harald Fricke; Jörg T Epplen; Martin Gencik
Novel SNPs in the CD18 gene validate the association with MPO-ANCA+ vasculitis.
Genes and immunity 2001;2(5):269-72.
2001: Ulrike Schara; Martin Gencik; J Mortier; M Langen; Alexandra Gencikova; Jörg T Epplen; Wilhelm Mortier
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: C Walter; Jeannette Gootjes; Petra A W Mooijer; H Portsteffen; C Klein; Hans R Waterham; Peter G Barth; Jörg T Epplen; Wolf-H Kunau; Ronald J A Wanders; Gabriele Dodt
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: W Mäueler; Gergis Bassili; Cornelia Hardt; HG Keyl; Jörg T Epplen
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: Rejko Krüger; Wilfried Kuhn; Klaus L Leenders; Reiner Sprengelmeyer; Thomas Müller; Dirk Woitalla; Axel T Portman; R P Maguire; L Veenma; U Schröder; Ludger Schöls; Jörg T Epplen; Olaf Riess; Horst Przuntek
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.
Neurology 2001;56(10):1355-62.
2001: Matthias Vorgerd; Martin Gencik; J Mortier; Jörg T Epplen; Jean-Pierre Malin; Wilhelm Mortier
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies.
Muscle & nerve 2001;24(3):421-4.
2001: Martin Gencik; Norbert Dahmen; Stefan Wieczorek; Meike Kasten; J Bierbrauer; Ion Anghelescu; Armin Szegedi; AM Menezes Saecker; Jörg T Epplen
A prepro-orexin gene polymorphism is associated with narcolepsy.
Neurology 2001;56(1):115-7.
2001: Martin Gencik; Norbert Dahmen; Stefan Wieczorek; Meike Kasten; Alexandra Gencikova; Jörg T Epplen
ApoE polymorphisms in narcolepsy.
BMC medical genetics 2001;2():9.
2001: Wolfram Klein; Andreas Tromm; Thomas Griga; Harald Fricke; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; Jörg T Epplen
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.
2000: Wolfram Klein; Andreas Tromm; Thomas Griga; Harald Fricke; Christian Folwaczny; Michael Hocke; Klaus Eitner; M Marx; M Runte; Jörg T Epplen
The IL-10 gene is not involved in the predisposition to inflammatory bowel disease.
Electrophoresis 2000;21(17):3578-82.
2000: Erdmute Kunstmann; Cornelia Hardt; E Elitok; M Harder; Sebastian Suerbaum; Ulrich Peitz; Wolff Schmiegel; Jörg T Epplen
The nonfunctional allele TCRBV6S1B is strongly associated with Helicobacter pylori infection.
Infection and immunity 2000;68(11):6493-5.
2000: Rejko Krüger; AM Menezes Saecker; Ludger Schöls; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Daniela Berg; K Berger; Horst Przuntek; Jörg T Epplen; Olaf Riess
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.
Neuroreport 2000;11(11):2439-42.
2000: Matthias Vorgerd; Ludger Schöls; Cornelia Hardt; Michael Ristow; Jörg T Epplen; Jochen Zange
Mitochondrial impairment of human muscle in Friedreich ataxia in vivo.
Neuromuscular disorders : NMD 2000;10(6):430-5.
2000: P Wintermeyer; Rejko Krüger; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Daniela Berg; G Becker; E Leroy; Mihael H Polymeropoulos; K Berger; Horst Przuntek; Ludger Schöls; Jörg T Epplen; Olaf Riess
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Neuroreport 2000;11(10):2079-82.
2000: Bianca Miterski; Rejko Krüger; P Wintermeyer; Jörg T Epplen
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: M Runte; Gabriele Dekomien; Jörg T Epplen
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: Gabriele Dekomien; Jörg T Epplen
Exclusion of the PDE6A gene for generalised progressive retinal atrophy in 11 breeds of dog.
Animal genetics 2000;31(2):135-9.
2000: Thomas Gerken; Thomas Lubjuhn; Jörg T Epplen
Low probe concentration can cause problems in multilocus DNA fingerprinting (cautionary notes III).
Electrophoresis 2000;21(3):554-5.
2000: F Tschentscher; A Kalt; Volker Hoffmann; Jörg T Epplen; Cornelia Hardt
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: Koen Vandenbroeck; Cornelia Hardt; J Louage; Pierre Fiten; S Jäckel; Isabelle Ronsse; Jörg T Epplen; Luigi M E Grimaldi; Tomas Olsson; Maria Giovanna Marrosu; An D Billiau; Ghislain Opdenakker
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: Dunja K Lamatsch; Indrajit Nanda; Jörg T Epplen; Michael Schmid; Manfred Schartl
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: Jörg T Epplen; Martin Gencik; A Epplen; Jürgen Andrich; Carsten Saft; Horst Przuntek
Morbus Huntington - a human genetic model disease.
Cytogenetics and cell genetics 2000;91(1-4):90-6.
2000: Gabriele Dekomien; M Runte; René Gödde; Jörg T Epplen
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: Rejko Krüger; Cornelia Hardt; F Tschentscher; S Jäckel; W Kuhn; Thomas Müller; J Werner; Dirk Woitalla; Daniela Berg; N Kühnl; G A Fuchs; Eduardo J M Santos; Horst Przuntek; Jörg T Epplen; Ludger Schöls; Olaf Riess
Genetic analysis of immunomodulating factors in sporadic Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2000;107(5):553-62.
2000: Martin Gencik; A Gencik; Wilhelm Mortier; Jörg T Epplen
Novel mutation in the RYR1 gene (R2454C) in a patient with malignant hyperthermia.
Human mutation 2000;15(1):122.
2000: Martin Gencik; S Meller; Stefan Borgmann; Thomas Sitter; AM Menezes Saecker; Harald Fricke; Jörg T Epplen
The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitides.
Clinical immunology (Orlando, Fla.) 2000;94(1):9-12.
1999: Bianca Miterski; S Jaeckel; Jörg T Epplen; Dieter Pöhlau; Cornelia Hardt
The interferon gene cluster: a candidate region for MS predisposition? Multiple Sclerosis Study Group.
Genes and immunity 1999;1(1):37-44.
1999: An Goris; C Epplen; Pierre Fiten; M Andersson; Raffaele Murru; Francesca L Sciacca; Isabelle Ronsse; S Jäckel; Jörg T Epplen; Maria Giovanna Marrosu; Tomas Olsson; Luigi M E Grimaldi; Ghislain Opdenakker; An D Billiau; Koen Vandenbroeck
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: Martin Gencik; Stefan Borgmann; R Zahn; E Albert; Thomas Sitter; Jörg T Epplen; Harald Fricke
Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis.
Clinical and experimental immunology 1999;117(2):412-7.
1999: Erdmute Kunstmann; C Epplen; E Elitok; M Harder; Sebastian Suerbaum; Ulrich Peitz; Wolff Schmiegel; Jörg T Epplen
Helicobacter pylori infection and polymorphisms in the tumor necrosis factor region.
Electrophoresis 1999;20(8):1756-61.
1999: Carola Borries; Kristin Launhardt; C Epplen; Jörg T Epplen; P Winkler
DNA analyses support the hypothesis that infanticide is adaptive in langur monkeys.
Proceedings. Biological sciences / The Royal Society 1999;266(1422):901-4.
1999: Rejko Krüger; AM Vieira-Saecker; Wilfried Kuhn; Daniela Berg; Thomas Müller; N Kühnl; G A Fuchs; A Storch; Marcel Hungs; Dirk Woitalla; Horst Przuntek; Jörg T Epplen; Ludger Schöls; Olaf Riess
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: R Koch; Martin Scholz; M R Nelen; K Schwechheimer; Jörg T Epplen; Albrecht Harders
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: Martin Gencik; Jörg T Epplen; Wilhelm Mortier
[Diagnosis of neuromuscular diseases: progress with molecular genetic techniques].
Deutsche medizinische Wochenschrift (1946) 1999;124(4):85-7.
1999: W Mäueler; Gergis Bassili; R Arnold; Rainer Renkawitz; Jörg T Epplen
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: W Mäueler; Gergis Bassili; C Epplen; HG Keyl; Jörg T Epplen
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: Rejko Krüger; A M Vieira-Säcker; Wilfried Kuhn; Thomas Müller; Dirk Woitalla; Ludger Schöls; Horst Przuntek; Jörg T Epplen; Olaf Riess
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: H C Peters; G Kämmer; A Volz; Klemens Kaupmann; Andreas Ziegler; B Bettler; Jörg T Epplen; T Sander; Olaf Riess
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: S Jaeckel; Jörg T Epplen; Marion Kauth; Bianca Miterski; F Tschentscher; C Epplen
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: Carsten Holzmann; W Mäueler; D Petersohn; T Schmidt; G Thiel; Jörg T Epplen; Olaf Riess
Isolation and characterization of the rat huntingtin promoter.
The Biochemical journal 1998;336 ( Pt 1)():227-34.
1998: T Schmidt; G Bernhard Landwehrmeyer; Iris Schmitt; Yvon Trottier; Georg Auburger; Franco Laccone; Thomas Klockgether; M Völpel; Jörg T Epplen; Ludger Schöls; Olaf Riess
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: C Epplen; I Over; Thomas Lubjuhn; Jörg T Epplen; K P Sauer
Genetic distinction of scorpionflies (Panorpa vulgaris) by microsatellites.
Molecular ecology 1998;7(9):1256-8.
1998: W Klein; Gabriele Dekomien; N Holmes; Jörg T Epplen
Evaluation of ROM1 as a candidate gene in generalised progressive retinal atrophy in dogs.
Animal genetics 1998;29(4):316-8.
1998: W Mäueler; A Kyas; HG Keyl; Jörg T Epplen
A genome-derived (gaa.ttc)24 trinucleotide block binds nuclear protein(s) specifically and forms triple helices.
Gene 1998;215(2):389-403.
1998: Kristin Launhardt; C Epplen; Jörg T Epplen; P Winkler
Amplification of microsatellites adapted from human systems in faecal DNA of wild Hanuman langurs (Presbytis entellus).
Electrophoresis 1998;19(8-9):1356-61.
1998: Ingo Schlupp; Indrajit Nanda; M Döbler; Dunja K Lamatsch; Jörg T Epplen; J Parzefall; Michael Schmid; Manfred Schartl
Dispensable and indispensable genes in an ameiotic fish, the Amazon molly Poecilia formosa.
Cytogenetics and cell genetics 1998;80(1-4):193-8.
1998: Jörg T Epplen; W Mäueler; Eduardo J M Santos
On GATAGATA and other "junk" in the barren stretch of genomic desert.
Cytogenetics and cell genetics 1998;80(1-4):75-82.
1998: Ludger Schöls; R Krüger; Georgios Amoiridis; Horst Przuntek; Jörg T Epplen; Olaf Riess
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
Journal of neurology, neurosurgery, and psychiatry 1998;64(1):67-73.
1997: Ludger Schöls; Georgios Amoiridis; Horst Przuntek; G Frank; Jörg T Epplen; C Epplen
Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
Brain : a journal of neurology 1997;120 ( Pt 12)():2131-40.
1997: Ludger Schöls; Georgios Amoiridis; T h Büttner; Horst Przuntek; Jörg T Epplen; Olaf Riess
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
Annals of neurology 1997;42(6):924-32.
1997: Ludger Schöls; Suzana Gispert; M Vorgerd; A M Menezes Vieira-Saecker; P Blanke; Georg Auburger; Georgios Amoiridis; S Meves; Jörg T Epplen; Horst Przuntek; Stef pulst; Olaf Riess
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.
Archives of neurology 1997;54(9):1073-80.
1997: C Epplen; Eduardo J M Santos; W Mäueler; P van Helden; Jörg T Epplen
On simple repetitive DNA sequences and complex diseases.
Electrophoresis 1997;18(9):1577-85.
1997: C Epplen; Jörg T Epplen; G Frank; Bianca Miterski; Eduardo J M Santos; Ludger Schöls
Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene.
Human genetics 1997;99(6):834-6.
1997: Olaf Riess; Franco Laccone; Suzana Gispert; Ludger Schöls; Christine Zühlke; AM Vieira-Saecker; S Herlt; Karl Wessel; Jörg T Epplen; Bernhard H F Weber; Friedmar R Kreuz; S Chahrokh-Zadeh; A Meindl; A Lunkes; J Aguiar; M Macek; A Krebsová; Milan Macek Jr.; Katrin Bürk; S Tinschert; I Schreyer; Stef pulst; Georg Auburger
SCA2 trinucleotide expansion in German SCA patients.
Neurogenetics 1997;1(1):59-64.
1997: Eduardo J M Santos; Jörg T Epplen; C Epplen
Extensive gene flow in human populations as revealed by protein and microsatellite DNA markers.
Human heredity 1997;47(3):165-72.
1997: A Haupt; Ludger Schöls; Horst Przuntek; Jörg T Epplen
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: Carsten Holzmann; A M Saecker; Jörg T Epplen; Olaf Riess
Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.
Journal of medical genetics 1997;34(3):264.
1997: C Epplen; S Jäckel; Eduardo J M Santos; M D'Souza; D Poehlau; B Dotzauer; Eckhart Sindern; Michael Haupts; K P Rüde; F Weber; J Stöver; S Poser; W Gehler; Jean-Pierre Malin; Horst Przuntek; Jörg T Epplen
Genetic predisposition to multiple sclerosis as revealed by immunoprinting.
Annals of neurology 1997;41(3):341-52.
1997: C Epplen; Eduardo J M Santos; João Farias Guerreiro; P van Helden; Jörg T Epplen
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: Ludger Schöls; Olaf Riess; Georgios Amoiridis; A Riess; Horst Przuntek; Jörg T Epplen
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
Fortschritte der Neurologie-Psychiatrie 1997;65(2):79-89.
1997: Olaf Riess; Jörg T Epplen; Georgios Amoiridis; Horst Przuntek; Ludger Schöls
Transmission distortion of the mutant alleles in spinocerebellar ataxia.
Human genetics 1997;99(2):282-4.