Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Altmueller, Janine Dr.med. 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Tauer S. Lorenz K.P. Lenzen A. Heils H. Muhle M. Gresch B.A. Neubauer S. Waltz G. Rudolf M. Mattheisen K. Strauch B. Schmitz U. Stephani T. Sander June 01, 2005 / Epilepsy Res Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy K.P. Lenzen A. Heils S. Lorenz A. Hempelmann T. Sander August 18, 2005 / Epilepsy Res A new EF-hand containing gene EFHC2 on Xp11.4: Tentative evidence for association with juvenile myoclonic epilepsy W. Gu T. Sander A. Heils K.P. Lenzen O.K. Steinlein July 01, 2005 / Epilepsy Res Neonatal seizures with tonic clonic sequences and poor developmental outcome B. Schmitt G. Wohlrab T. Sander O.K. Steinlein B.L. Hajnal September 09, 2005 / Cell Role of endocytosis in cellular uptake of sex steroids A. Hammes T.K. Andreassen R. Spoelgen J. Raila N. Huebner H. Schulz J. Metzger F.J. Schweigert P.B. Luppa A. Nykjaer T.E. Willnow October 01, 2005 / Epilepsia Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy K.P. Lenzen A. Heils S. Lorenz A. Hempelmann T. Sander January 01, 2005 / Nat Genet Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 L.A. Metherell J.P. Chapple S. Cooray A. David C. Becker F. Rueschendorf D. Naville M. Begeot B. Khoo P. Nuernberg A. Huebner M.E. Cheetham A.J.L. Clark January 01, 2005 / Bioinformatics ALOHOMORA: a tool for linkage analysis using 10K SNP array data F. Rueschendorf P. Nuernberg January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann Pagination Current page 1 Page 2 Page 3 Next page Next › Last page Last »
January 01, 2005 / Ann Neurol Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy U. Tauer S. Lorenz K.P. Lenzen A. Heils H. Muhle M. Gresch B.A. Neubauer S. Waltz G. Rudolf M. Mattheisen K. Strauch B. Schmitz U. Stephani T. Sander
June 01, 2005 / Epilepsy Res Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy K.P. Lenzen A. Heils S. Lorenz A. Hempelmann T. Sander
August 18, 2005 / Epilepsy Res A new EF-hand containing gene EFHC2 on Xp11.4: Tentative evidence for association with juvenile myoclonic epilepsy W. Gu T. Sander A. Heils K.P. Lenzen O.K. Steinlein
July 01, 2005 / Epilepsy Res Neonatal seizures with tonic clonic sequences and poor developmental outcome B. Schmitt G. Wohlrab T. Sander O.K. Steinlein B.L. Hajnal
September 09, 2005 / Cell Role of endocytosis in cellular uptake of sex steroids A. Hammes T.K. Andreassen R. Spoelgen J. Raila N. Huebner H. Schulz J. Metzger F.J. Schweigert P.B. Luppa A. Nykjaer T.E. Willnow
October 01, 2005 / Epilepsia Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy K.P. Lenzen A. Heils S. Lorenz A. Hempelmann T. Sander
January 01, 2005 / Nat Genet Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 L.A. Metherell J.P. Chapple S. Cooray A. David C. Becker F. Rueschendorf D. Naville M. Begeot B. Khoo P. Nuernberg A. Huebner M.E. Cheetham A.J.L. Clark
January 01, 2005 / Bioinformatics ALOHOMORA: a tool for linkage analysis using 10K SNP array data F. Rueschendorf P. Nuernberg
January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst
January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann