J. Genschel

O. Landt, J. Genschel, H. Lochs, 2004, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Quantification of Lipoprotein(a): Comparison of an Automated Latex-Enhanced Nephelometric Assay with an Immunoenzymometric Method

M. Manns, J. Genschel, H. Schmidt, 1996, European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies.

LMNA Mutations in Cardiac Transplant Recipients

P. Flemming, A. Haverich, M. Wilhelmi, 2005, Cardiology.

A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy

R. Hetzer, R. Ewert, J. Genschel, 2001 .

Three novel mutations, c314C>A, C778insC, and c1285+2T>A, in exon 2 of the Wilson disease gene

M. Manns, J. Genschel, B. Bochow, 2000, Human mutation.

A new frameshift mutation at codon 466 (1397delA) within the LMNA gene

R. Hetzer, R. Ewert, J. Genschel, 2000, Human mutation.

A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.

R. Hetzer, R. Ewert, J. Genschel, 2001, Human mutation.

FH clinical phenotype in Greek patients with LDL‐R defective vs. negative mutations

G. Dedoussis, C. Stefanadis, C. Pitsavos, 2004, European journal of clinical investigation.

Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA gene.

J. Genschel, H. Lochs, J. Ockenga, 2001, The Journal of clinical endocrinology and metabolism.

Apolipoprotein A‐I induced amyloidosis

J. Genschel, H. Schmidt, R. Haas, 1998, FEBS letters.

Long‐term treatment experience in a subject with Dunnigan‐type familial partial lipodystrophy: efficacy of rosiglitazone

J. Genschel, H. Worman, H. Mehnert, 2005, Diabetic medicine : a journal of the British Diabetic Association.

Lipid Evaluation in HIV-1-Positive Patients Treated with Protease Inhibitors

M. Manns, R. Schmidt, J. Genschel, 1998, Antiviral therapy.

A Q136Stop mutation in the ARH gene causing autosomal recessive hypercholesterolaemia with severely delayed LDL catabolism

J. Genschel, U. Tietge, H. Schmidt, 2003, Journal of internal medicine.

Molecular characterization of familial hypercholesterolemia in German and Greek patients

P. Toutouzas, G. Dedoussis, C. Pitsavos, 2004 .

LDL‐receptor mutations in Europe

G. Dedoussis, J. Genschel, H. Schmidt, 2004, Human mutation.

Mutations in the LMNA gene encoding lamin A/C

J. Genschel, H. Schmidt, 2000, Human mutation.

The c.1-260C>T Promoter Variant of CD14 but Not the c.896A>G (p.D299G) Variant of Toll-Like Receptor 4 (TLR4) Genes Is Associated with Inflammatory Bowel Disease

F. Nagy, B. Wiedenmann, J. Genschel, 2007, Digestion.

Introducing Genetic Testing for Adult-Type Hypolactasia

M. Worm, J. Genschel, H. Lochs, 2005, Digestion.

Inhibition of Transthyretin-met30 Expression Using Inosine15.1-Hammerhead Ribozymes in Cell Culture

M. Manns, S. Kubicka, J. Genschel, 2000 .

Inhibition of transthyretin-met30 expression using Inosine(15.1)-Hammerhead ribozymes in cell culture.

M. Manns, S. Kubicka, J. Genschel, 2000, Biochemical and biophysical research communications.

Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease

A. Członkowska, J. Genschel, B. Bochow, 2001, Human Mutation.

The interleukin-25 gene located in the inflammatory bowel disease (IBD) 4 region: no association with inflammatory bowel disease.

J. Genschel, H. Lochs, H. Schmidt, 2003, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

The c.1-260C>T Promoter Variant of CD14 but Not the c.896A>G (p.D299G) Variant of Toll-Like Receptor 4 (TLR4) Genes Is Associated with Inflammatory Bowel Disease

F. Nagy, B. Wiedenmann, J. Genschel, 2007, Digestion.

LDL‐receptor mutations in Europe

G. Dedoussis, J. Genschel, H. Schmidt, 2005 .

A new LMNA mutation causing limb girdle muscular dystrophy 1B

M. Gutberlet, S. Zinn-Justin, B. Gilquin, 2005, Journal of Neurology.