Universität zu Köln

Journal Article

Bai, Hanwen, Harmanci, Akdes Serin, Erson-Omay, E. Zeynep, Li, Jie, Coskun, Sueleyman, Simon, Matthias, Krischek, Boris, Ozduman, Koray ORCID: 0000-0002-3543-0401, Omay, S. Buelent, Sorensen, Eric A., Turcan, Sevin ORCID: 0000-0002-0885-5607, Bakirciglu, Mehmet, Carrion-Grant, Geneive, Murray, Phillip B., Clark, Victoria E., Ercan-Sencicek, A. Gulhan, Knight, James, Sencar, Leman, Altinok, Selin, Kaulen, Leon D., Guelez, Burcu, Timmer, Marco, Schramm, Johannes, Mishra-Gorur, Ketu, Henegariu, Octavian, Moliterno, Jennifer, Louvi, Angeliki, Chan, Timothy A., Tannheimer, Stacey L., Pamir, M. Necmettin, Vortmeyer, Alexander O., Bilguvar, Kaya, Yasuno, Katsuhito ORCID: 0000-0002-3606-532X and Guenel, Murat (2016). Integrated genomic characterization of IDH1-mutant glioma malignant progression. Nature Genet., 48 (1). S. 59 - 70. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

Clarke, Victoria E., Harmanci, Akdes Serin, Bai, Hanwen, Youngblood, Mark W., Lee, Tong Ihn, Baranoski, Jacob F., Ercan-Sencicek, A. Gulhan, Abraham, Brian J., Weintraub, Abraham S., Hnisz, Denes ORCID: 0000-0002-6256-1693, Simon, Matthias, Krischek, Boris, Erson-Omay, E. Zeynep, Henegariu, Octavian, Carrion-Grant, Geneive, Mishra-Gorur, Ketu, Duran, Daniel ORCID: 0000-0001-6888-252X, Goldmann, Johanna E., Schramm, Johannes, Goldbrunner, Roland, Piepmeier, Joseph M., Vortmeyer, Alexander O., Gunel, Jennifer Molitemo, Bilguvar, Kaya, Yasuno, Katsuhito ORCID: 0000-0002-3606-532X, Young, Richard A. and Gunel, Murat (2016). Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas. Nature Genet., 48 (10). S. 1253 - 1260. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Muller, Juliane S., Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie ORCID: 0000-0003-4900-9877, Santorelli, Filippo M., Alfares, Ahmed A., Zhu, Changlian, Meszarosova, Anna Uhrova, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R., Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T., Strom, Tim M., De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana ORCID: 0000-0001-8939-1447, Alfadhel, Majid, van de Warrenburg, Bart P., Portier, Ruben, Bergmann, Carsten, Firouzabadi, Saghar Ghasemi, Jin, Sheng Chih ORCID: 0000-0002-5777-7262, Bilguvar, Kaya, Hamed, Sherifa ORCID: 0000-0002-1441-3530, Abdelhameed, Mohammed, Haridy, Nourelhoda A., Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W., Mau-Them, Frederic Tran, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele ORCID: 0000-0003-4788-9719, Zara, Federico ORCID: 0000-0001-9744-5222, Salpietro, Vincenzo, Scala, Marcello ORCID: 0000-0003-2194-7239, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laetitia, Schmitt, Emmanuelle, Lacaze, Elodie, Kupper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J. H., Grand, Katheryn, Graham, John M., Lewis, Richard A., Millan, Francisca, Duman, Ozgur, Dundar, Nihal, Uyanik, Gokhan, Schols, Ludger ORCID: 0000-0001-7774-5025, Nurnberg, Peter, Nurnberg, Gudrun, Bordes, Andrea Catala, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Boucanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S., Shamseldin, Hanan, Al Tala, Saeed, Varaghchi, Jamileh Rezazadeh, Najafi, Maryam, Deschner, Selina, Glaser, Dieter, Huttel, Wolfgang, Kruer, Michael C., Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Zuchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schuele, Rebecca, Horvath, Rita ORCID: 0000-0002-9841-170X, Houlden, Henry, Bartesaghi, Luca ORCID: 0000-0001-8218-4648, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark ORCID: 0000-0003-1985-3671 and Senderek, Jan (2021). Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain, 144 (5). S. 1422 - 1435. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Muller, Juliane S., Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie ORCID: 0000-0003-4900-9877, Santorelli, Filippo M., Alfares, Ahmed A., Zhu, Changlian, Meszarosova, Anna Uhrova, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R., Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T., Strom, Tim M., De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana ORCID: 0000-0001-8939-1447, Alfadhel, Majid, van de Warrenburg, Bart P., Portier, Ruben, Bergmann, Carsten, Firouzabadi, Saghar Ghasemi, Jin, Sheng Chih ORCID: 0000-0002-5777-7262, Bilguvar, Kaya, Hamed, Sherifa ORCID: 0000-0002-1441-3530, Abdelhameed, Mohammed, Haridy, Nourelhoda A., Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W., Mau-Them, Frederic Tran, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele ORCID: 0000-0003-4788-9719, Zara, Federico ORCID: 0000-0001-9744-5222, Salpietro, Vincenzo, Scala, Marcello ORCID: 0000-0003-2194-7239, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laetitia, Schmitt, Emmanuelle, Lacaze, Elodie, Kuepper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J. H., Grand, Katheryn, Graham, John M., Jr., Lewis, Richard A., Millan, Francisca, Duman, Ozgur, Dundar, Nihal, Uyanik, Gokhan, Schols, Ludger ORCID: 0000-0001-7774-5025, Nuernberg, Peter, Nuernberg, Gudrun, Bordes, Andrea Catala, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Boucanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S., Shamseldin, Hanan, Al Tala, Saeed, Varaghchi, Jamileh Rezazadeh, Najafi, Maryam, Deschner, Selina, Glaeser, Dieter, Huettel, Wolfgang, Kruer, Michael C., Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Zuchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schuele, Rebecca, Horvath, Rita ORCID: 0000-0002-9841-170X, Houlden, Henry, Bartesaghi, Luca ORCID: 0000-0001-8218-4648, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark ORCID: 0000-0003-1985-3671 and Senderek, Jan (2021). Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain, 144. S. 1422 - 1435. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Youngblood, Mark W., Duran, Daniel ORCID: 0000-0001-6888-252X, Montejo, Julio D., Li, Chang, Omay, Sacit Bulent, Ozduman, Koray, Sheth, Amar H., Zhao, Amy Y., Tyrtova, Evgeniya, Miyagishima, Danielle F., Fomchenko, Elena, I, Hong, Christopher S., Clark, Victoria E., Riche, Maximilien, Peyre, Matthieu, Boetto, Julien, Sohrabi, Sadaf, Koljaka, Sarah, Baranoski, Jacob F., Knight, James, Zhu, Hongda, Pamir, M. Necmettin, Avsar, Timucin, Kilic, Turker, Schramm, Johannes, Timmer, Marco, Goldbrunner, Roland, Gong, Ye, Bayri, Yasar, Amankulor, Nduka, Hamilton, Ronald L., Bilguvar, Kaya, Tikhonova, Irina, Tomak, Patrick R., Huttner, Anita, Simon, Matthias, Krischek, Boris, Kalamarides, Michel, Erson-Omay, E. Zeynep, Moliterno, Jennifer and Guenel, Murat (2020). Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomas. J. Neurosurg., 133 (5). S. 1345 - 1355. ROLLING MEADOWS: AMER ASSOC NEUROLOGICAL SURGEONS. ISSN 1933-0693