Items where Greenwich Author is "Asadollahi, Dr Reza"

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Number of items: 37.

32GM007753 from the National Institute of General Medical Sciences

Harris, Holly K, Nakayama, Tojo, Lai, Jenny, Zhao, Boxun, Argyrou, Nikoleta, Gubbels, Cynthia S, Soucy, Aubrie, Genetti, Casie A, Suslovitch, Victoria, Rodan, Lance H, Tiller, George E, Lesca, Gaetan, Gripp, Karen W, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Hamosh, Ada, Applegate, Carolyn D, Turnpenny, Peter D, Simon, Marleen E H, Volker-Touw, Catharina M L, Van Gassen, Koen L I, Binsbergen, Ellen van, Pfundt, Rolph, Gardeitchik, Thatjana, De Vries, Bert B A, Immken, LaDonna L, Buchanan, Catherine, Willing, Marcia, Toler, Tomi L, Fassi, Emily, Baker, Laura, Vansenne, Fleur, Wang, Xiadong, Ambrus Jr, Julian L, Fannemel, Madeleine, Posey, Jennifer E, Agolini, Emanuele, Novelli, Antonio, Rauch, Anita, Boonsawat, Paranchai, Fagerberg, Christina R, Larsen, Martin J, Kibaek, Maria, Labalme, Audrey, Poisson, Alice, Payne, Katelyn K, Walsh, Laurence E, Aldinger, Kimberly A, Balciuniene, Jorune, Skraban, Cara, Gray, Christopher, Murrell, Jill, Bupp, Caleb P, Pascolini, Giulia, Grammatico, Paola, Broly, Martin, Küry, Sébastien, Nizon, Mathilde, Rasool, Iqra Ghulam, Zahoor, Muhammad Yasir, Kraus, Cornelia, Reis, André, Iqbal, Muhammad, Uguen, Kevin, Audebert-Bellanger, Severine, Ferec, Claude, Redon, Sylvia, Baker, Janice, Wu, Yunhong, Zampino, Guiseppe, Syrbe, Steffan, Brosse, Ines, Abou Jamra, Rami, Dobyns, William B, Cohen, Lilian L, Blomhoff, Anne, Mignot, Cyril, Keren, Boris, Courtin, Thomas, Agrawal, Pankaj B, Beggs, Alan H and Yu, Timothy W (2021) Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior. Genetics in Medicine, 23 (6). pp. 1028-1040. ISSN 1098-3600 (Print), 1530-0366 (Online) (doi:10.1038/s41436-021-01114-z)

Bavarian Ministry of Education and Culture, Science and the Arts

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Delvendahl, Igor, Muff, Rebecca, Tan, Ge, Rodríguez, Daymé González, Turan, Soeren, Russo, Martina, Oneda, Beatrice, Joset, Pascal, Boonsawat, Paranchai, Masood, Rahim, Mocera, Martina, Ivanovski, Ivan, Baumer, Alessandra, Bachmann-Gagescu, Ruxandra, Schlapbach, Ralph, Rehrauer, Hubert, Steindl, Katharina, Begemann, Anaïs, Reis, André, Winkler, Jürgen, Winner, Beate, Müller, Martin and Rauch, Anita (2023) Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons. Human Molecular Genetics, 32 (13). pp. 2192-2204. ISSN 0964-6906 (Print), 1460-2083 (Online) (doi:10.1093/hmg/ddad048)

Bavarian Ministry of Education and Culture, Science and the Arts within the framework of the Bavarian Network for Induced Pluripotent Stem Cells: ForIPS

Popp, Bernt ORCID: https://orcid.org/0000-0002-3679-1081, Krumbiegel, Mandy, Grosch, Janina, Sommer, Annika, Uebe, Steffen, Kohl, Zacharias ORCID: https://orcid.org/0000-0002-4147-8866, Plötz, Sonja, Farrell, Michaela, Trautmann, Udo, Kraus, Cornelia, Ekici, Arif B. ORCID: https://orcid.org/0000-0001-6099-7066, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Regensburger, Martin ORCID: https://orcid.org/0000-0002-2172-7386, Günther, Katharina, Rauch, Anita, Edenhofer, Frank, Winkler, Jürgen, Winner, Beate and Reis, André ORCID: https://orcid.org/0000-0002-6301-6363 (2018) Need for high-resolution genetic analysis in iPSC: results and lessons from the ForIPS consortium. Scientific reports, 8:17201. ISSN 2045-2322 (Online) (doi:10.1038/s41598-018-35506-0)

Bavarian Ministry of Education and Culture, Science and the Arts within the framework of the Bavarian Network for studying brain cell interactions: ForInter

Krumm, Laura, Pozner, Tatyana, Kaindl, Johanna, Regensburger, Martin, Günther, Claudia, Turan, Soeren, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Rauch, Anita and Winner, Beate (2021) Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in. Stem Cell Research, 56:102520. ISSN 1873-5061 (doi:10.1016/j.scr.2021.102520)

Bavarian Molecular Biosystems Research Network: BioSysNet, the German Federal Ministry of Education and Research (BMBF: 01GQ113, 01GM1520A, 01EK1609B)

Baylor-Hopkins Center for Mendelian Genomics (BHCMG, UM1 HG006542)

Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 270949263/GRK2162

ERA-NET grant “Euromicro” (SNF 31ER30_154238 to AR) and radiz–Rare Disease Initiative Zurich, clinical research priority program, University of Zurich

Boonsawat, Paranchai, Joset, Pascal, Steindl, Katharina, Oneda, Beatrice, Gogoll, Laura, Azzarello-Burri, Silvia, Sheth, Frenny, Datar, Chaitanya, Verma, Ishwar C., Puri, Ratna Dua, Zollino, Marcella, Bachmann-Gagescu, Ruxandra, Niedrist, Dunja, Papik, Michael, Figueiro-Silva, Joana, Masood, Rahim, Zweier, Markus, Kraemer, Dennis, Lincoln, Sharyn, Rodan, Lance, Passemard, Sandrine, Drunat, Séverine, Verloes, Alain, Horn, Anselm H.C., Sticht, Heinrich, Steinfeld, Robert, Plecko, Barbara, Latal, Beatrice, Jenni, Oskar, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564 and Rauch, Anita (2019) Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly. Genetics in Medicine, 21 (9). pp. 2043-2058. ISSN 1098-3600 (Print), 1530-0366 (Online) (doi:10.1038/s41436-019-0464-7)

European Research Council (Grant No. SynDegrade-679881)

Forschungskredit of the University of Zurich

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Oneda, Beatrice, Sheth, Frenny, Azzarello-Burri, Silvia, Baldinger, Rosa, Joset, Pascal, Latal, Beatrice, Knirsch, Walter, Desai, Soaham, Baumer, Alessandra, Houge, Gunnar, Andrieux, Joris and Rauch, Anita (2013) Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. European Journal of Human Genetics, 21 (10). pp. 1100-1104. ISSN 1018-4813 (Print), 1476-5438 (Online) (doi:10.1038/ejhg.2013.17)

Forschungskredit of the University of Zurich (grant number 54220201)

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Strauss, Justin E, Zenker, Martin, Beuing, Oliver ORCID: https://orcid.org/0000-0001-8033-063X, Edvardson, Simon, Elpeleg, Orly, Strom, Tim M, Joset, Pascal, Niedrist, Dunja, Otte, Christine, Oneda, Beatrice, Boonsawat, Paranchai, Azzarello-Burri, Silvia, Bartholdi, Deborah, Papik, Michael, Zweier, Markus, Haas, Cordula, Ekici, Arif B ORCID: https://orcid.org/0000-0001-6099-7066, Baumer, Alessandra, Boltshauser, Eugen, Steindl, Katharina, Nothnagel, Michael ORCID: https://orcid.org/0000-0001-8305-7114, Schinzel, Albert, Stoeckli, Esther T and Rauch, Anita ORCID: https://orcid.org/0000-0003-2930-3163 (2018) Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling. European Journal of Human Genetics, 26 (2). pp. 197-209. ISSN 1018-4813 (Print), 1476-5438 (Online) (doi:10.1038/s41431-017-0019-9)

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Oneda, Beatrice, Joset, Pascal, Azzarello-Burri, Silvia, Bartholdi, Deborah, Steindl, Katharina, Vincent, Marie, Cobilanschi, Joana, Sticht, Heinrich, Baldinger, Rosa, Reissmann, Regina, Sudholt, Irene, Thiel, Christian T, Ekici, Arif B, Reis, André, Bijlsma, Emilia K, Andrieux, Joris, Dieux, Anne, FitzPatrick, David, Ritter, Susanne, Baumer, Alessandra, Latal, Beatrice, Plecko, Barbara, Jenni, Oskar G and Rauch, Anita (2014) The clinical significance of small copy number variants in neurodevelopmental disorders. Journal of Medical Genetics, 51 (10). pp. 677-688. ISSN 0022-2593 (Print), 1468-6244 (Online) (doi:10.1136/jmedgenet-2014-102588)

French Ministry of Health and the Health Regional Agency from Bretagne, Pays de la Loire and Centre Val de Loire (HUGODIMS 2, 2017)

German Federal Ministry of Education and Research funded treat HSP consortium (01GM1905B and grants 01GQ113, 01GM1520A, 01EK1609B)

Health Innovation Challenge Fund (Grant No. HICF-1009-003)

Boonsawat, Paranchai, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Niedrist, Dunja, Steindl, Katharina, Begemann, Anaïs, Joset, Pascal, Bhoj, Elizabeth J., Li, Dong, Zackai, Elaine, Vetro, Annalisa, Barba, Carmen, Guerrini, Renzo, Whalen, Sandra, Keren, Boris, Khan, Amjad, Jing, Duan, Palomares Bralo, María, Rikeros Orozco, Emi, Hao, Qin, Schlott Kristiansen, Britta, Zheng, Bixia, Donnelly, Deirdre, Clowes, Virginia, Zweier, Markus, Papik, Michael, Siegel, Gabriele, Sabatino, Valeria, Mocera, Martina, Horn, Anselm H.C., Sticht, Heinrich and Rauch, Anita ORCID: https://orcid.org/0000-0003-2930-3163 (2024) Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling. American Journal of Human Genetics. ISSN 0002-9297 (Print), 1537-6605 (Online) (doi:10.1016/j.ajhg.2024.07.016)

Italian Ministry of Health

NIH/NIMH R01MH113761, NICHD/NHGRI/NIH U19HD077671 and NIH/NICHD U24HD0938487

National Institute for Health Research

National Institutes of Health (NIH) Common Fund, through the Office of Strategic Coordination/Office of the NIH Director under award number U01HG007690

Swiss National Science Foundation

Swiss National Science Foundation (Grant No. 320020_179547)

Swiss National Science Foundation (Grant No. 320020_17954; PZ00P3_174018)

Swiss National Science Foundation (SNF 320030_135669)

Swiss National Science Foundation (SNSF) grant 320030_179547

Begemann, Anaïs, Acuña, Mario A., Zweier, Markus, Vincent, Marie, Steindl, Katharina, Bachmann-Gagescu, Ruxandra, Hackenberg, Annette, Abela, Lucia, Plecko, Barbara, Kroell-Seger, Judith, Baumer, Alessandra, Yamakawa, Kazuhiro, Inoue, Yushi, Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Sticht, Heinrich, Zeilhofer, Hanns Ulrich and Rauch, Anita (2019) Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes. Molecular Medicine, 25 (1). ISSN 1076-1551 (Print), 1528-3658 (Online) (doi:10.1186/s10020-019-0073-6)

Tom Wahlig Stiftung

University Research Priority Program of the University of Zurich

University of Zurich

University of Zurich Clinical Research Priority Program

Wellcome Trust (Grant No. WT098051)

Wellcome Trust Sanger Institute [grant number WT098051] (Nature 2015;519:223-8)

Wellcome Trust and the UK Department of Health Innovation Challenge Fund [HICF-1009-003]

radiz–Rare Disease Initiative Zurich, clinical research priority program, University of Zurich

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Zweier, Markus, Gogoll, Laura, Schiffmann, Raphael, Sticht, Heinrich ORCID: https://orcid.org/0000-0001-5644-045X, Steindl, Katharina and Rauch, Anita (2017) Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation. European Journal of Medical Genetics, 60 (9). pp. 451-464. ISSN 1769-7212 (doi:10.1016/j.ejmg.2017.06.004)

radiz—Rare Disease Initiative Zürich, Clinical Research Priority Program for Rare Diseases of the University of Zurich

von Sick Foundation

Asadollahi, Reza ORCID: https://orcid.org/0000-0002-1497-0564, Britschgi, Christian, Joset, Pascal, Oneda, Beatrice, Schindler, Detlev ORCID: https://orcid.org/0000-0003-2451-8165, Meier, Urs R. and Rauch, Anita ORCID: https://orcid.org/0000-0003-2930-3163 (2020) Severe reaction to radiotherapy provoked by hypomorphic germline mutations in ATM (ataxia–telangiectasia mutated gene). Molecular Genetics and Genomic Medicine, 8 (10):e1409. ISSN 2324-9269 (Online) (doi:10.1002/mgg3.1409)

This list was generated on Sun Dec 22 03:07:34 2024 UTC.