Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Acevedo Ochoa, Ernesto (1) Adami, Eleonora Dr. (19) Ahmad, Ata Ul Wakeel (1) Aigner, Denise (1) Akalin, Altuna Dr. (73) Akmeric, Emir Bora (2) Albrecht, Jan Philipp (5) Alenina, Natalia Dr. (174) Ali, Mohammed Ahmed Khallaf Dr. (1) Alp, Keziban Merve (3) Altmueller, Janine Dr.med. (308) Anandakumar, Harithaa (2) Annibale, Paolo Dr. (25) Apaydin, Onur (2) Arnau Soler, Aleix Dr. (5) Bachtler, Barbara (1) Bader, Michael Prof. Dr. (687) Badillo Lisakowski, Victor Christian Dr. (3) Bahr, Lina Samira Dr. (2) Bähring, Sylvia Dr. (51) Bahry, Ella Dr. (3) Barke, Niclas (1) Bartels-Klein, Eireen (9) Bartolomaeus, Hendrik (22) Bartolomaeus, Theda (15) Bauersachs, Daniel (1) Baumann, Elisabeth (4) Bayram, Safak (4) Begay-Müller, Valerie Dr. (23) Beier, Christin (1) Bemmann, Franziska (1) Benlasfer, Nouhad (2) Bernert, Carola (4) Berruezo Llacuna, Maria (2) Beule, Dieter Dr. (90) Birchmeier, Walter Prof. Dr. (206) Birchmeier-Kohler, Carmen Prof. Dr. (173) Birkner, Till (10) Birol, Melissa Dr. (12) Blachut, Susanne (6) Blankenstein, Thomas Prof. Dr. (179) Blume, Alexander Dr. (8) Blüthgen, Nils (21) Bock-Bierbaum, Tobias Dr. (5) Bonsor, Megan (1) Born, Gabriele (1) Borodina, Tatiana Dr. (10) Bosco, Bartolomeo Dr. (1) Bouman, Brigitte Joanne (2) Braeuning, Caroline (6) Brouwer-Lehmitz, Antje Susan (1) Brüning, Ulrike Dr. (4) Bunina, Daria Dr. (11) Bunse, Mario Dr. (16) Burkert, Christian Martin (3) Cakmak-Görür, Nese Dr. (2) Cano Rincon, Elena Dr. (8) Carneiro Raimundo, Sandra Cristina Dr. (1) Carvalho, Silvia Filipa (2) Castilho de Barros, Carlos Prof. Dr. (6) Cerda Esteban, Nuria Dr. (3) Cerda Jara, Cledi Alicia (3) Cetin, Ali Osman (1) Chakrabarti, Sampurna Dr. (3) Chekulaeva, Marina Dr. (21) Chen, Chia-Yu (5) Chen, Wei Prof. Dr. (146) Chu, Van Trung Dr. (22) Chu, Xiaofeng (1) Cibin, Penelope (1) Clauß, Julian (2) Cöl Arslan, Seda Dr. (7) Collins, Russell Thomas Dr. (8) Conrad, Thomas Dr. (16) Coralluzzo, Violeta (1) Coscia, Fabian Dr. (26) Costanza, Mariantonia Dr. (5) Crocini, Claudia Dr. (3) Dahlmann, Mathias Dr. (29) Dang Ngoc, Tu Dr. (2) Daniel, Peter Prof. Dr. (100) Dartsch, Josephine (7) Daumke, Oliver Prof. Dr. (92) Dechend, Ralf Priv. 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(299) de la Rosa, Kathrin Prof. Dr. (22) Del Giudice, Simone (2) del Rey Mateos, Sara Adelaida (1) Deter, Aylina (1) Diebolder, Christoph Dr. (16) Diecke, Sebastian Dr. (75) Dietrich, Carola (1) Di Virgilio, Michela Prof. Dr. (28) Dörr, Jan Rafael (8) Dräger, Alexander (5) Dramaretska, Yuliia (5) Driesner, Madlen (2) Dube, Giuliana Marie (1) Dyck, Lydia Dr. (1) Edes, Inan Dr. (4) Eisenberger, Alina (3) Emmenegger, Lisa (1) Endemann, Beate Dr. (3) Escobar Fernandez, Helena Dr. (14) Espejo Oltra, Jose Andres (1) Essex, Morgan (4) Estebanez, Luc Dr. (4) Ezquerra Romano, Ivan Dr. (1) Fälber, Katja Dr. (14) Falcke, Martin Prof. Dr. (114) Falk, Kirsten Dr. (27) Farre i Diaz, Carlota (2) Faxel, Miriam (1) Feinkohl, Insa Prof. Dr. (36) Fentker, Kerstin Johanna (3) Fernández Ochoa, Álvaro Dr. (12) Ferri Blazquez, Alba Maria (1) Fielitz, Jens Dr. (60) Filosa, Alessandro Dr. (11) Fischer, Christian (7) Fischer, Cornelius Dr. (21) Forbes, Martin Dr. (6) Forslund, Sofia Dr. (121) Frahm-Barske, Silke Dr. (13) Franke, Vedran Dr. (22) Franz, Kristina Dr.rer.medic. 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(44) Haase, Nadine Dr. (37) Haghverdi, Laleh Dr. (14) Hammes-Lewin, Annette Dr. (30) Hänig, Christian (12) Harabula, Izabela-Cezara (10) Hartl, Kimberly (4) Haseleu, Julia Dr. (5) Haucke, Volker Professor (30) Hedtrich, Sarah Prof. Dr. (86) Heinemann, Udo Prof. Dr. (135) Henssen, Anton Prof. Dr. med. (64) Herse, Florian PD Dr. (93) Herzog, Margareta (6) Herzog, Sergej (2) Heuser, Arnd Dr. (48) Hinz, Michael Dr. (17) Hinze, Christian Dr. med. Dipl.-Math. 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(22) León Perinán, Daniel (1) Leutz, Achim Prof. Dr. (100) Lewin, Gary Prof. Dr. (154) Li, Rui (1) Li, Xinqi (1) Liang, Ning Dr. (1) Lindberg, Eric Lars-Helge (10) Lisek, Kamil Dr. (2) Lisewski, Ulrike Dr. (9) Lisowski, Pawel Dr. (22) Liu, Tiannan (2) Löber, Ulrike Dr. (31) Lohse, Martin Prof. Dr. (45) Lopez Carballo, Jacobo (3) Lorenz, Felix Dr. (6) Ludwig, Leif S. Dr. med. Dr. rer. nat. 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Januar 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 01. Januar 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark 07. Januar 2005 / Am J Respir Crit Care Med Genomewide linkage analysis identifies novel genetic loci for lung function in mice C. Reinhard B. Meyer H. Fuchs T. Stoeger G. Eder F. Rueschendorf J. Heyder P. Nuernberg M. Hrabe de Angelis H. Schulz 30. Dezember 2005 / BMC Genet Linkage analysis of alcohol dependence using MOD scores K. Strauch R. Fuerst F. Rueschendorf C. Windemuth J. Dietter A. Flaquer M.P. Baur T.F. Wienker 01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann 01. November 2005 / Am J Hum Genet Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator C.T. Thiel D. Horn B. Zabel A.B. Ekici K. Salinas E. Gebhart F. Rueschendorf H. Sticht J. Spranger D. Mueller C. Zweier M.E. Schmitt A. Reis A. Rauch 01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi 30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman 01. Juni 2019 / Front Neurol Linkage evidence for a two-locus inheritance of LQT-associated seizures in a multigenerational LQT family with a novel KCNQ1 loss-of-function mutation H. Prüss G. Gessner S.H. Heinemann F. Rüschendorf A.K. Ruppert H. Schulz T. Sander W. Rimpau 01. Juni 2018 / J Invest Dermatol SMARCAD1 haploinsufficiency underlies Huriez syndrome and associated skin cancer susceptibility C. Günther M.A. Lee-Kirsch J. Eckhard A. Matanovic T. Kerscher F. Rüschendorf B. Klein N. Berndt N. Zimmermann C. Flachmeier T. Thuß N. Lucas I. Marenholz J. Esparza-Gordillo N. Hübner H. Traupe E. Delaporte Y.A. Lee Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous Seite 1 Aktuelle Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
01. Januar 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
01. Januar 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark
07. Januar 2005 / Am J Respir Crit Care Med Genomewide linkage analysis identifies novel genetic loci for lung function in mice C. Reinhard B. Meyer H. Fuchs T. Stoeger G. Eder F. Rueschendorf J. Heyder P. Nuernberg M. Hrabe de Angelis H. Schulz
30. Dezember 2005 / BMC Genet Linkage analysis of alcohol dependence using MOD scores K. Strauch R. Fuerst F. Rueschendorf C. Windemuth J. Dietter A. Flaquer M.P. Baur T.F. Wienker
01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann
01. November 2005 / Am J Hum Genet Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator C.T. Thiel D. Horn B. Zabel A.B. Ekici K. Salinas E. Gebhart F. Rueschendorf H. Sticht J. Spranger D. Mueller C. Zweier M.E. Schmitt A. Reis A. Rauch
01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi
30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman
01. Juni 2019 / Front Neurol Linkage evidence for a two-locus inheritance of LQT-associated seizures in a multigenerational LQT family with a novel KCNQ1 loss-of-function mutation H. Prüss G. Gessner S.H. Heinemann F. Rüschendorf A.K. Ruppert H. Schulz T. Sander W. Rimpau
01. Juni 2018 / J Invest Dermatol SMARCAD1 haploinsufficiency underlies Huriez syndrome and associated skin cancer susceptibility C. Günther M.A. Lee-Kirsch J. Eckhard A. Matanovic T. Kerscher F. Rüschendorf B. Klein N. Berndt N. Zimmermann C. Flachmeier T. Thuß N. Lucas I. Marenholz J. Esparza-Gordillo N. Hübner H. Traupe E. Delaporte Y.A. Lee