Rappold, Gudrun Prof. Dr. rer. nat.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Schmitteckert, Stefanie (10)
- Gretz, Norbert (1954-2023) (8)
- Fröhlich, Henning (8)
- Wöginger, Simone (8)
- Decker, Eva (8)
- Bacon, Claire (7)
- Moog, Ute (7)
- Endris, Volker (7)
- Fischer, Christine (7)
- Lasitschka, Felix (7)
- Durand, Claudia (6)
- Paramasivam, Nagarajan (6)
- Blaschke, Rüdiger Jörg (6)
- Rietschel, Marcella (6)
- Glaser, Anne (5)
- Sticht, Carsten (5)
- Sprengel, Rolf (5)
- Wogatzky, Birgit (5)
- Granzow, Martin (5)
- Jauch, Anna (4)
- Kirsch, Stefan (4)
- Bettendorf, Markus (4)
- Martinez, Cristina (4)
- Marchini, Antonio (4)
- Fukami, Maki (4)
- Eckstein, Volker (4)
- Bartsch, Dusan (3)
- Heinrich, Udo (3)
- Montalbano, Antonino (3)
- Rafiullah, Rafiullah (3)
- Sumer, Simon (3)
- Cristian, Flavia-Bianca (3)
- Griesbeck, Anne (3)
- (weitere Einträge vorhanden...)
Co-Autoren (extern)
- Mertz, Annelyse (4)
- Petit, Christine (4)
- Matsuo, Nobutake (4)
- Propping, Peter (1942-2016) (3)
- Vick, Philipp (3)
- Nöthen, Markus Maria (3)
- Kääb, Stefan (3)
- Kutsche, Kerstin (3)
- Palka, Giandomenico (3)
- Toder, Roland (3)
- Winkelmann, Martina (3)
- Wapenaar, Martin C. (3)
- Stuppia, Liborio (3)
- Meder, J. (2)
- Emons, Joyce (2)
- D'Amato, Mauro (2)
- Koenen, Michael (2)
- Albus, Margot (2)
- Rauch, Anita (2)
- Binder, Gerhard (2)
- Prabhakar, Prab (2)
- Klier, Ina (2)
- Lindsay, Susan (2)
- Dobyns, William B. (2)
- Zirn, Birgit (2)
- Lehrach, Hans (2)
- Coubes, Christine (2)
- Oehl-Jaschkowitz, Barbara (2)
- Ciccodicola, Alfredo (2)
- Villard, Laurent (2)
- Pilz, Daniela T. (2)
- Jarvis, Joanna (2)
- Isidor, Bertrand (2)
- (weitere Einträge vorhanden...)
Neueste Publikationen in heiBIB 
(ingesamt sind 194 Publikationen erfasst)
- Werren, Elizabeth A.: Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations / Elizabeth A. Werren, Emily R. Peirent, Henna Jantti, Alba Guxholli, Kinshuk Raj Srivastava, Naama Or… , 2024. - 15 S. : Illustrationen
In: Cell death & disease, ISSN 2041-4889. 15 (2024), Article number 379, Seite [1]-15
DOI: 10.1038/s41419-024-06768-6
- Rappold, Gudrun: 10 years of international albinism awareness : United Nations celebrate an anniversary and a decade of collective progress, but challenges remain / Gudrun A. Rappold, 2024-09-05. - 2 S. : Illustrationen
In: Medizinische Genetik, ISSN 1863-5490. 36(2024), 3, Seite 217-218
DOI: 10.1515/medgen-2024-2032
- Rappold, Gudrun: Celebrating the 100th anniversary of the Japan Endocrine Society and international collaborations / Gudrun A. Rappold, Ph.D., 2024. - 2 S. : Illustrationen
In: Endocrine journal, ISSN 1348-4540. 71(2024), 9, Seite 825-826
DOI: 10.1507/endocrj.EJ20240112
- Weiß, Birgit: Identification of novel genes including NAV2 associated with isolated tall stature / Birgit Weiss, Tim Ott, Philipp Vick, Julian C. Lui, Ralph Roeth, Sebastian Vogel, Stephan Waldmüller… , 12 December 2023. - 11 S.
In: Frontiers in endocrinology, ISSN 1664-2392. 14(2023) vom: Dez., Artikel-ID 1258313, Seite 1-11
DOI: 10.3389/fendo.2023.1258313
- Rädecke, Kristin: Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 / Kristin Rädecke, Ambuj Gore, Karin Burau, Magdalena Laugsch, Katrin Köhler, Gudrun A Rappold, Sandra… , 5 April 2023. - 7 S.
In: Stem cell research, ISSN 1876-7753. 69(2023) vom: Apr., Artikel-ID 103089, Seite 1-7
DOI: 10.1016/j.scr.2023.103089
- Berens, Sabrina: Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome : a multicenter retrospective study / Sabrina Berens, Yuanjun Dong, Nikola Fritz, Jutta Walstab, Mauro D'Amato, Tenghao Zheng, Verena Wahl… , June 7, 2022. - 16 S.
In: World journal of gastroenterology, ISSN 2219-2840. 28(2022), 21, Seite 2334-2349
DOI: 10.3748/wjg.v28.i21.2334
- Wang, Jing: Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome / Jing Wang, Henning Fröhlich, Felipe Bodaleo Torres, Rangel Leal Silva, Gernot Poschet, Amit Agarwal,… , February 14, 2022. - 11 S.
In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 1091-6490. 119(2022), 8, Artikel-ID e2112852119, Seite 1-11
DOI: 10.1073/pnas.2112852119
- Wang, Jing: Disrupted mitochondrial network drives deficits of learning and memory in a mouse model of FOXP1 haploinsufficiency / Jing Wang, Gudrun A. Rappold and Henning Fröhlich, 11 January 2022. - 12 S.
In: Genes, ISSN 2073-4425. 13(2022), 1, Artikel-ID 127, Seite 1-12
DOI: 10.3390/genes13010127
- Eltokhi, Ahmed: Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disorders / Ahmed Eltokhi, Miguel A.Gonzalez-Lozano, Lars-Lennart Oettl, Andrey Rozov, Claudia Pitzer, Ralph Röt… , 21 May 2021. - 23 S.
In: Molecular psychiatry, ISSN 1476-5578. 26(2021), Seite 6482-6504
DOI: 10.1038/s41380-021-01140-y
- Vick, Philipp: Identification of ZBTB26 as a novel risk factor for congenital hypothyroidism / Philipp Vick, Birgit Eberle, Daniela Choukair, Birgit Weiss, Ralph Roeth, Isabelle Schneider, Nagara… , 19 November 2021. - 1 Online-Ressource S. : Ilustrationen, Diagramme
In: Genes, ISSN 2073-4425. 12(2021), 12, Artikel-ID 1862, Seite 1-10
DOI: 10.3390/genes12121862
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