Daniela Steinberger

bio.logis digital health gmbh, frankfurt am main, germany

29H指数

234论文数

3.2K被引数

收录论文 25

发表时间

Clinical Implementation of Pharmacogenomics and Drug–Drug Interaction Screening in a German Academic Teaching Hospital and Outpatient Follow-Up 德国教学医院中药物基因组学与药物-药物相互作用筛查的临床实施及门诊随访

Clinical Pharmacology & Therapeutics

IF5.5

2025-10-11

OAAI

Roman Tremmel; Filippa Schreeck; Simon Jaeger; Severin Schricker; Elke Schaeffeler; Svitlana Igel; Daniela Steinberger; Manuel Pagitz; Jörg Latus; Markus Ketteler; Kerstin Bühl; Marc-H. Dahlke; Hans-Georg Kopp; Matthias Schwab

Pharmacogenetic Implementation Studies—Lessons Learned From the PREPARE Study 药物基因组学实施研究——来自PREPARE研究的经验教训

Clinical Pharmacology & Therapeutics

IF5.5

2025-06-24

OAAI

Henk-Jan Guchelaar; Cathelijne H. van der Wouden; Lisanne E. N. Manson; Heshu Abdullah-Koolmees; Kathrin Blagec; Tanja Blagus; Stefan Böhringer; Erika Cecchin; Ka-Chun Cheung; Vera H. M. Deneer; Siv Jonsson; Candace Joefield-Roka; Katja S. Just; Mats O. Karlsson; Lidija Konta; Rudolf Koopmann; Marjolein Kriek; Thorsten Lehr; Christina Mitropoulou; Victoria Rollinson; Rossana Roncato; Matthias Samwald; Elke Schaeffeler; Maria Skokou; Matthias Schwab; Daniela Steinberger; Julia C. Stingl; Roman Tremmel; Richard M. Turner; Mandy H. van Rhenen; Cristina L. Dávila-Fajardo; Vita Dolžan; George P. Patrinos; Munir Pirmohamed; Gere Sunder-Plassmann; Giuseppe Toffoli; Jesse J. Swen; Ubiquitous Pharmacogenomics Consortium

Joint analysis of germline genetic data from over 29,000 cases with suspected hereditary breast and ovarian cancer (HBOC) as part of the NASGE initiative

BREAST

IF7.9

2025-04-01

OAAI

Henkel, Jan; Laner, Andreas; Locher, Melanie; Wohlfrom, Tobias; Neitzel, Birgit; Becker, Kerstin; Neuhann, Teresa; Abicht, Angela; Steinke-Lange, Verena; Klink, Barbara; Eichhorn, Birgit; Schmidt, Winfried; Berner, Daniel; Teubert, Anna; Holtorf, Anne; Heinrich, Sarah; Wildhardt, Gabriele; Schulze, Martin; von der Heyden, Laura; Hoertnagel, Konstanze; Steinberger, Daniela; Kleier, Saskia; Lorenz, Peter; Glaubitz, Ralf; Biskup, Saskia; Holinski-Feder, Elke

A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study 预防药物不良反应的12基因药物遗传学小组: 一项开放标签，多中心，对照，集群随机交叉实施研究

LANCET

IF88.5

2023-02-01

221

PREAI

Swen, Jesse J.; van der Wouden, Cathelijne H.; Manson, Lisanne E. N.; Abdullah-Koolmees, Heshu; Blagec, Kathrin; Blagus, Tanja; Boehringer, Stefan; Cambon-Thomsen, Anne; Cecchin, Erika; Cheung, Ka-Chun; Deneer, Vera H. M.; Dupui, Mathilde; Ingelman-Sundberg, Magnus; Jonsson, Siv; Joefield-Roka, Candace; Just, Katja S.; Karlsson, Mats O.; Konta, Lidija; Koopmann, Rudolf; Kriek, Marjolein; Lehr, Thorsten; Mitropoulou, Christina; Rial-Sebbag, Emmanuelle; Rollinson, Victoria; Roncato, Rossana; Samwald, Matthias; Schaeffeler, Elke; Skokou, Maria; Schwab, Matthias; Steinberger, Daniela; Stingl, Julia C.; Tremmel, Roman; Turner, Richard M.; van Rhenen, Mandy H.; Fajardo, Cristina L. Davila; Dolzan, Vita; Patrinos, George P.; Pirmohamed, Munir; Sunder-Plassmann, Gere; Toffoli, Giuseppe; Guchelaar, Henk-Jan

Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium

CLINICAL PHARMACOLOGY & THERAPEUTICS

IF5.5

2017-02-13

227

PREAI

van der Wouden, C. H.; Cambon-Thomsen, A.; Cecchin, E.; Cheung, K. C.; Davila-Fajardo, C. L.; Deneer, V. H.; Dolzan, V.; Ingelman-Sundberg, M.; Jonsson, S.; Karlsson, M. O.; Kriek, M.; Mitropoulou, C.; Patrinos, G. P.; Pirmohamed, M.; Samwald, M.; Schaeffeler, E.; Schwab, M.; Steinberger, D.; Stingl, J.; Sunder-Plassmann, G.; Toffoli, G.; Turner, R. M.; Van Rhenen, Mh; Swen, J. J.; Guchelaar, H-J

EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO

HUMAN MUTATION

IF3.7

2017-01-23

OAAI

Skopkova, Martina; Hennig, Friederike; Shin, Byung-Sik; Turner, Clesson E.; Stanikova, Daniela; Brennerova, Katarina; Stanik, Juraj; Fischer, Ute; Henden, Lyndal; Mueller, Ulrich; Steinberger, Daniela; Leshinsky-Silver, Esther; Bottani, Armand; Kurdiova, Timea; Ukropec, Jozef; Nyitrayova, Olga; Kolnikova, Miriam; Klimes, Iwar; Borck, Guntram; Bahlo, Melanie; Haas, Stefan A.; Kim, Joo-Ran; Lotspeich-Cole, Leda E.; Gasperikova, Daniela; Dever, Thomas E.; Kalscheuer, Vera M.

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

MOLECULAR PSYCHIATRY

IF10.1

2015-02-03

245

OAAI

Hu, H.; Haas, S. A.; Chelly, J.; Van Esch, H.; Raynaud, M.; de Brouwer, A. P. M.; Weinert, S.; Froyen, G.; Frints, S. G. M.; Laumonnier, F.; Zemojtel, T.; Love, M. I.; Richard, H.; Emde, A-K; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; Wissink-Lindhout, W.; Lebrun, N.; Castelnau, L.; Rucci, J.; Montjean, R.; Dorseuil, O.; Billuart, P.; Stuhlmann, T.; Shaw, M.; Corbett, M. A.; Gardner, A.; Willis-Owen, S.; Tan, C.; Friend, K. L.; Belet, S.; van Roozendaal, K. E. P.; Jimenez-Pocquet, M.; Moizard, M-P; Ronce, N.; Sun, R.; O'Keeffe, S.; Chenna, R.; Van Boemmel, A.; Goeke, J.; Hackett, A.; Field, M.; Christie, L.; Boyle, J.; Haan, E.; Nelson, J.; Turner, G.; Baynam, G.; Gillessen-Kaesbach, G.; Mueller, U.; Steinberger, D.; Budny, B.; Badura-Stronka, M.; Latos-Bielenska, A.; Ousager, L. B.; Wieacker, P.; Criado, G. Rodriguez; Bondeson, M-L; Anneren, G.; Dufke, A.; Cohen, M.; Van Maldergem, L.; Vincent-Delorme, C.; Echenne, B.; Simon-Bouy, B.; Kleefstra, T.; Willemsen, M.; Fryns, J-P; Devriendt, K.; Ullmann, R.; Vingron, M.; Wrogemann, K.; Wienker, T. F.; Tzschach, A.; van Bokhoven, H.; Gecz, J.; Jentsch, T. J.; Chen, W.; Ropers, H-H; Kalscheuer, V. M.

Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection 通过长期人类巨细胞病毒感染选择高度侵入性的神经母细胞瘤细胞群

ONCOGENESIS

IF6.4

2012-04-30

OAAI

Michaelis, M.; Barth, S.; Breitling, R.; Bruch, J.; Steinberger, D.; Rothweiler, F.; Hackmann, K.; Schroeck, E.; Doerr, H. W.; Griffin, D. K.; Cinatl, J.; Cinatl, J., Jr.

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain

JOURNAL OF MEDICAL GENETICS

IF3.7

2009-07-02

103

OAAI

Chen, J.; Wildhardt, G.; Zhong, Z.; Roeth, R.; Weiss, B.; Steinberger, D.; Decker, J.; Blum, W. F.; Rappold, G.

A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome 单等位基因双突变导致TNF受体相关的周期性发热综合征

RHEUMATOLOGY INTERNATIONAL

IF2.9

2009-06-23

OAAI