Karl Martin Klein

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 15

Top Venues

Epilepsia

Epilepsia open

Journal of neurology

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Karl Martin Klein, Rumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, Tatiana Maroilley, Navprabhjot Kaur, Yiping Liu, Tyler Soule, Minette Manalo, Goichiro Tamura, Julia Jacobs, Walter Hader, Gerald Pfeffer, Maja Tarailo-Graovac
Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique. Epilepsia 65 (6) (2024)
Karl Martin Klein, Rumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, Tatiana Maroilley, Navprabhjot Kaur, Yiping Liu, Tyler Soule, Minette Manalo, Goichiro Tamura, Julia Jacobs, Walter Hader, Gerald Pfeffer, Maja Tarailo-Graovac
Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique. Epilepsia 65 (6) (2024)
Karl Martin Klein, Rumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, Tatiana Maroilley, Navprabhjot Kaur, Yiping Liu, Tyler Soule, Minette Manalo, Goichiro Tamura, Julia Jacobs, Walter Hader, Gerald Pfeffer, Maja Tarailo-Graovac
Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique. Epilepsia (2024)
Mark A Corbett, Christel Depienne, Liana Veneziano, Karl Martin Klein, Francesco Brancati, Renzo Guerrini, Federico Zara, Shoji Tsuji, Jozef Gecz
Genetics of Familial Adult Myoclonus Epilepsy: From linkage studies to non-coding repeat expansions. Epilepsia (2023)
Sophie von Brauchitsch, Denise Haslinger, Silvia Lindlar, Holger Thiele, Natalie Bernsen, Felix Zahnert, Philipp S Reif, Yunus Balcik, Ping Yee Billie Au, Colin B Josephson, Janine Altmüller, Adam Strzelczyk, Susanne Knake, Felix Rosenow, Andreas Chiocchetti, Karl Martin Klein
The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing. Epilepsia open (2023)
Guillermo Delgado-García, Jordan D T Engbers, Samuel Wiebe, Pauline Mouches, Kimberly Amador, Nils D Forkert, James White, Tolulope T Sajobi, Karl Martin Klein, Colin Bruce Josephson, null null
Machine learning using multimodal clinical, electroencephalographic, and magnetic resonance imaging data can predict incident depression in adults with epilepsy: A pilot study. Epilepsia (2023)
Tatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, Catherine Diao, Maryam Khanbabaei, Sabine Kaya, Christel Depienne, Maja Tarailo-Graovac, Karl Martin Klein
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia open (2023)
Tatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, Catherine Diao, Maryam Khanbabaei, Sabine Kaya, Christel Depienne, Maja Tarailo-Graovac, Karl Martin Klein
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia open (2023)
Sophie von Brauchitsch, Denise Haslinger, Silvia Lindlar, Holger Thiele, Natalie Bernsen, Felix Zahnert, Philipp S Reif, Yunus Balcik, Ping Yee Billie Au, Colin Bruce Josephson, Janine Altmüller, Adam Strzelczyk, Susanne Knake, Felix Rosenow, Andreas Chiocchetti, Karl Martin Klein
The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing. Epilepsia open (2023)
Simona Balestrini, Daniela Chiarello, Maria Gogou, Katri Silvennoinen, Clinda Puvirajasinghe, Wendy D Jones, Philipp Reif, Karl Martin Klein, Felix Rosenow, Yvonne G Weber, Holger Lerche, Susanne Schubert-Bast, Ingo Borggraefe, Antonietta Coppola, Serena Troisi, Rikke S Møller, Antonella Riva, Pasquale Striano, Federico Zara, Cheryl Hemingway, Carla Marini, Anna Rosati, Davide Mei, Martino Montomoli, Renzo Guerrini, J Helen Cross, Sanjay M Sisodiya
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. Journal of neurology, neurosurgery, and psychiatry 92 (10) (2021)
Christina Cherian, Juan Pablo Appendino, Setareh Ashtiani, Paolo Federico, Christine P Molnar, Marina Kerr, Aneal Khan, Ping Yee Billie Au, Karl Martin Klein
The phenotypic spectrum of KCNT1: a new family with variable epilepsy syndromes including mild focal epilepsy. Journal of neurology (2021)
Marianne Hrabok, Jordan D T Engbers, Samuel Wiebe, Tolulope T Sajobi, Ann Subota, Amal Almohawes, Paolo Federico, Alexandra Hanson, Karl Martin Klein, Joseph Samuel Peedicail, Neelan Pillay, Shaily Singh, Colin Bruce Josephson
Primary care electronic medical records can be used to predict risk and identify potentially modifiable factors for early and late death in adult onset epilepsy. Epilepsia 62 (1) (2020)
Rahel T Florian, Florian Kraft, Elsa Leitão, Sabine Kaya, Stephan Klebe, Eloi Magnin, Anne-Fleur van Rootselaar, Julien Buratti, Theresa Kühnel, Christopher Schröder, Sebastian Giesselmann, Nikolai Tschernoster, Janine Altmueller, Anaide Lamiral, Boris Keren, Caroline Nava, Delphine Bouteiller, Sylvie Forlani, Ludmila Jornea, Regina Kubica, Tao Ye, Damien Plassard, Bernard Jost, Vincent Meyer, Jean-François Deleuze, Yannick Delpu, Mario D M Avarello, Lisanne S Vijfhuizen, Gabrielle Rudolf, Edouard Hirsch, Thessa Kroes, Philipp S Reif, Felix Rosenow, Christos Ganos, Marie Vidailhet, Lionel Thivard, Alexandre Mathieu, Thomas Bourgeron, Ingo Kurth, Haloom Rafehi, Laura Steenpass, Bernhard Horsthemke, null null, Eric LeGuern, Karl Martin Klein, Pierre M Labauge, Mark F Bennett, Melanie Bahlo, Jozef Gecz, Mark A Corbett, Marina A J Tijssen, Arn M J M van den Maagdenberg, Christel Depienne
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3. Nature communications 10 (1) (2019)
Mark A Corbett, Thessa Kroes, Liana Veneziano, Mark F Bennett, Rahel Florian, Amy L Schneider, Antonietta Coppola, Laura Licchetta, Silvana Franceschetti, Antonio Suppa, Aaron Wenger, Davide Mei, Manuela Pendziwiat, Sabine Kaya, Massimo Delledonne, Rachel Straussberg, Luciano Xumerle, Brigid Regan, Douglas Crompton, Anne-Fleur van Rootselaar, Anthony Correll, Rachael Catford, Francesca Bisulli, Shreyasee Chakraborty, Sara Baldassari, Paolo Tinuper, Kirston Barton, Shaun Carswell, Martin Smith, Alfredo Berardelli, Renee Carroll, Alison Gardner, Kathryn L Friend, Ilan Blatt, Michele Iacomino, Carlo Di Bonaventura, Salvatore Striano, Julien Buratti, Boris Keren, Caroline Nava, Sylvie Forlani, Gabrielle Rudolf, Edouard Hirsch, Eric Leguern, Pierre Labauge, Simona Balestrini, Josemir W Sander, Zaid Afawi, Ingo Helbig, Hiroyuki Ishiura, Shoji Tsuji, Sanjay M Sisodiya, Giorgio Casari, Lynette G Sadleir, Riaan van Coller, Marina A J Tijssen, Karl Martin Klein, Arn M J M van den Maagdenberg, Federico Zara, Renzo Guerrini, Samuel Frank Berkovic, Tommaso Pippucci, Canafoglia Laura, Melanie Bahlo, Pasquale Striano, Ingrid Eileen Scheffer, Francesco Brancati, Christel Depienne, Jozef Gecz
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2. Nature communications 10 (1) (2019)
Karl Martin Klein, Manuela Pendziwiat, Anda Eilam, Ronit Gilad, Ilan Blatt, Felix Rosenow, Moien Kanaan, Ingo Helbig, Zaid Afawi, null null
The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizures. Journal of neurology 264 (7) (2017)

Karl Martin Klein.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Karl Martin Klein