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K

Katarina Cisarova

Medical University of Graz
H指数:12
被引数:906

个人简介

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教育背景

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工作经历

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荣誉奖项

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SRSF2 P95H induces monocytic priming of human hematopoietic stem and progenitor cells

SRSF2 P95H诱导人造血干细胞和祖细胞的单核细胞前体状态

Leukemia
IF13.4
2026-09-140
OAAI
Johannes Foßelteder; Gabriel Pabst; Andrea Raicht; Tommaso Sconocchia; Angelika Schlacher; Lisa Auinger; Daniel Martinez-Krams; Asiri Ediriwickrema; Katarina Vizar-Cisarova; Peter Schlenke; Annkristin Heine; Heinz Sill; Armin Zebisch; Ravindra Majeti; Andreas Reinisch
Aberrant methylation limits antitumoral inflammation in lung adenocarcinoma by restricting RIPK3 expression
Science Advances
IF12.5
2026-01-210
OAAI
Deepti Agrawal; Katarina Cisarova; Sebastian Vosberg; Fabian Allmendinger; Enkhtsetseg Munkhbaatar; Nadia Dandachi; Francisco Jose Fernandez Hernandez; Marta Tonietto; Vanessa Jäger; Martina Anton; Eva C. Keller; Moritz Jesinghaus; Anna-Lena Meinhardt; Verena Haefner; Tobias Stoeger; Katja Steiger; Nicholas McGranahan; Michael A. Dengler; Adam Wahida; Philipp J. Jost
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2025-04-010
PRE
Guillouet, Charlotte; Agostini, Valeria; Baujat, Genevieve; Cocciadiferro, Dario; Pippucci, Tommaso; Lesieur-Sebellin, Marion; Georget, Mathieu; Schatz, Ulrich; Fauth, Christine; Louie, Raymond J.; Rogers, Curtis; Davis, Jessica M.; Konstantopoulou, Vassiliki; Mayr, Johannes A.; Bouman, Arjan; Wilke, Martina; VanNoy, Grace E.; England, Eleina M.; Park, Kristen L.; Brown, Kathleen; Saenz, Margarita; Novelli, Antonio; Digilio, Maria Cristina; Mastromoro, Gioia; Rongioletti, Mauro Ciro Antonio; Piacentini, Gerardo; Kaiyrzhanov, Rauan; Guliyeva, Sughra; Hasanova, Lala; Shears, Deborah; Bhatnagar, Ishita; Stals, Karen; Klaas, Oliver; Horvath, Judit; Bouvagnet, Patrice; Witmer, P. Dane; MacCarrick, Gretchen; Cisarova, Katarina; Good, Jean-Marc; Gorokhova, Svetlana; Boute, Odile; Smol, Thomas; Bruel, Ange-Line; Patat, Olivier; Broadbent, Julia R.; Tan, Tiong Y.; Tan, Natalie B.; Lyonnet, Stanislas; Busa, Tiffany; Graziano, Claudio; Amiel, Jeanne; Gordon, Christopher T.
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures

在智力障碍，发育退化和社会认知缺陷但无癫痫发作的患者中发现CACNA1E的从头变体

MOLECULAR AUTISM
IF5.5
2021-10-2615
OAAI
Royer-Bertrand, Beryl; Gygax, Marine Jequier; Cisarova, Katarina; Rosenfeld, Jill A.; Bassetti, Jennifer A.; Moldovan, Oana; O'Heir, Emily; Burrage, Lindsay C.; Allen, Jake; Emrick, Lisa T.; Eastman, Emma; Kumps, Camille; Abbas, Safdar; Van Winckel, Geraldine; Chabane, Nadia; Zackai, Elaine H.; Lebon, Sebastien; Keena, Beth; Bhoj, Elizabeth J.; Umair, Muhammad; Li, Dong; Donald, Kirsten A.; Superti-Furga, Andrea
A live single-cell reporter assay links intratumor heterogeneity to metastatic proclivity in Ewing sarcoma

活细胞报告分析将尤文肉瘤的肿瘤内异质性与转移倾向联系起来

SCIENCE ADVANCES
IF12.5
2021-07-025
OAAI
Keskin, Tugba; Rucci, Beatrice; Cornaz-Buros, Sandrine; Martin, Patricia; Fusco, Carlo; Broye, Liliane; Cisarova, Katarina; Perez, Elizabeth M.; Letovanec, Igor; La Rosa, Stefano; Cherix, Stephane; Diezi, Manuel; Renella, Raffaele; Provero, Paolo; Suva, Mario L.; Stamenkovic, Ivan; Riggi, Nicolo
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa

通过全基因组关联研究检测到的EYS中的一种拟态变异有助于色素性视网膜炎

COMMUNICATIONS BIOLOGY
IF5.1
2021-01-2912
OAAI
Nishiguchi, Koji M.; Miya, Fuyuki; Mori, Yuka; Fujita, Kosuke; Akiyama, Masato; Kamatani, Takashi; Koyanagi, Yoshito; Sato, Kota; Takigawa, Toru; Ueno, Shinji; Tsugita, Misato; Kunikata, Hiroshi; Cisarova, Katarina; Nishino, Jo; Murakami, Akira; Abe, Toshiaki; Momozawa, Yukihide; Terasaki, Hiroko; Wada, Yuko; Sonoda, Koh-Hei; Rivolta, Carlo; Tsunoda, Tatsuhiko; Tsujikawa, Motokazu; Ikeda, Yasuhiro; Nakazawa, Toru
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy
NATURE COMMUNICATIONS
IF15.7
2019-06-2832
OAAI
Nikopoulos, Konstantinos; Cisarova, Katarina; Quinodoz, Mathieu; Koskiniemi-Kuendig, Hanna; Miyake, Noriko; Farinelli, Pietro; Rehman, Atta Ur; Khan, Muhammad Imran; Prunotto, Andrea; Akiyama, Masato; Kamatani, Yoichiro; Terao, Chikashi; Miya, Fuyuki; Ikeda, Yasuhiro; Ueno, Shinji; Fuse, Nobuo; Murakami, Akira; Wada, Yuko; Terasaki, Hiroko; Sonoda, Koh-Hei; Ishibashi, Tatsuro; Kubo, Michiaki; Cremers, Frans P. M.; Kutalik, Zoltan; Matsumoto, Naomichi; Nishiguchi, Koji M.; Nakazawa, Toru; Rivolta, Carlo
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2016-09-0151
OAAI
Nikopoulos, Konstantinos; Farinelli, Pietro; Giangreco, Basilio; Tsika, Chrysanthi; Royer-Bertrand, Beryl; Mbefo, Martial K.; Bedoni, Nicola; Kjellstrom, Ulrika; El Zaoui, Ikram; Di Gioia, Silvio Alessandro; Balzano, Sara; Cisarova, Katarina; Messina, Andrea; Decembrini, Sarah; Plainis, Sotiris; Blazaki, Styliani V.; Khan, Muhammad Imran; Micheal, Shazia; Boldt, Karsten; Ueffing, Marius; Moulin, Alexandre P.; Cremers, Frans P. M.; Roepman, Ronald; Arsenijevic, Yvan; Tsilimbaris, Miltiadis K.; Andreasson, Sten; Rivolta, Carlo

研究方向

暂未获取到该数据
C
Carlo Rivolta
H 指数:55论文数:292被引数:1.9万
B
Béryl Royer‐Bertrand
H 指数:17论文数:35被引数:1,306
M
Mathieu Quinodoz
H 指数:25论文数:111被引数:4,619
V
Virginie G. Peter
H 指数:13论文数:32被引数:642
R
Rosanna Pescini Gobert
H 指数:17论文数:22被引数:1,206
A
Andrea Superti‐Furga
H 指数:83论文数:732被引数:2.6万
A
Alexandre Moulin
H 指数:28论文数:215被引数:3,660
I
Ikram El Zaoui
H 指数:9论文数:15被引数:479
P
Philipp J. Jost
H 指数:39论文数:272被引数:1.5万
S
Serge Leyvraz
H 指数:56论文数:369被引数:1.4万