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论文共 227 篇作者统计合作学者相似作者

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Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer,Tzung-Chien Hsieh,Hartmut Engels, Sophia Peters,Alexej Knaus,Shahida Moosa,Luisa Averdunk, Felix Boschann,Henrike Lisa Sczakiel,Sarina Schwartzmann, Martin Atta Mensah,Jean Tori Pantel,Manuel Holtgrewe, Annemarie Bösch,Claudia Weiß,Natalie Weinhold, Aude-Annick Suter,Corinna Stoltenburg, Julia Neugebauer, Tillmann Kallinich,Angela M Kaindl, Susanne Holzhauer, Christoph Bührer,Philip Bufler, Uwe Kornak, Claus-Eric Ott, Markus Schülke,Hoa Huu Phuc Nguyen,Sabine Hoffjan,Corinna Grasemann,Tobias Rothoeft, Folke Brinkmann,Nora Matar, Sugirthan Sivalingam,Claudia Perne,Elisabeth Mangold,Martina Kreiss,Kirsten Cremer, Regina C Betz,Martin Mücke,Lorenz Grigull,Thomas Klockgether,Isabel Spier,André Heimbach, Tim Bender,Fabian Brand,Christiane Stieber, Alexandra Marzena Morawiec,Pantelis Karakostas,Valentin S Schäfer, Sarah Bernsen, Patrick Weydt, Sergio Castro-Gomez, Ahmad Aziz,Marcus Grobe-Einsler,Okka Kimmich,Xenia Kobeleva, Demet Önder,Hellen Lesmann,Sheetal Kumar,Pawel Tacik, Meghna Ahuja Basin, Pietro Incardona,Min Ae Lee-Kirsch,Reinhard Berner, Catharina Schuetz, Julia Körholz,Tanita Kretschmer,Nataliya Di Donato,Evelin Schröck,André Heinen,Ulrike Reuner, Amalia-Mihaela Hanßke,Frank J Kaiser,Eva Manka,Martin Munteanu, Alma Kuechler,Kiewert Cordula,Raphael Hirtz, Elena Schlapakow, Christian Schlein,Jasmin Lisfeld, Christian Kubisch,Theresia Herget,Maja Hempel, Christina Weiler-Normann, Kurt Ullrich, Christoph Schramm,Cornelia Rudolph, Franziska Rillig, Maximilian Groffmann,Ania Muntau, Alexandra Tibelius,Eva M C Schwaibold, Christian P Schaaf, Michal Zawada,Lilian Kaufmann,Katrin Hinderhofer, Pamela M Okun,Urania Kotzaeridou,Georg F Hoffmann,Daniela Choukair,Markus Bettendorf, Malte Spielmann, Annekatrin Ripke,Martje Pauly,Alexander Münchau, Katja Lohmann,Irina Hüning,Britta Hanker, Tobias Bäumer,Rebecca Herzog,Yorck Hellenbroich,Dominik S Westphal,Tim Strom, Reka Kovacs,Korbinian M Riedhammer,Katharina Mayerhanser,Elisabeth Graf,Melanie Brugger,Julia Hoefele, Konrad Oexle,Nazanin Mirza-Schreiber,Riccardo Berutti,Ulrich Schatz,Martin Krenn,Christine Makowski,Heike Weigand,Sebastian Schröder,Meino Rohlfs,Katharina Vill,Fabian Hauck,Ingo Borggraefe,Wolfgang Müller-Felber,Ingo Kurth, Miriam Elbracht,Cordula Knopp,Matthias Begemann,Florian Kraft,Johannes R Lemke,Julia Hentschel,Konrad Platzer,Vincent Strehlow,Rami Abou Jamra, Martin Kehrer, German Demidov,Stefanie Beck-Wödl,Holm Graessner, Marc Sturm, Lena Zeltner,Ludger J Schöls,Janine Magg,Andrea Bevot,Christiane Kehrer,Nadja Kaiser,Ernest Turro,Denise Horn, Annette Grüters-Kieslich, Christoph Klein, Stefan Mundlos,Markus Nöthen,Olaf Riess,Thomas Meitinger,Heiko Krude,Peter M Krawitz,Tobias Haack, Nadja Ehmke, Matias Wagner
Nature geneticsno. 8 (2024): 1644-1653
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GestaltMatcher Database - A Global Reference for Facial Phenotypic Variability in Rare Human Diseases
Hellen Lesmann,Alexander Hustinx,Shahida Moosa,Hannah Klinkhammer,Elaine Marchi,Pilar Caro, Ibrahim M Abdelrazek,Jean Tori Pantel, Merle Ten Hagen,Meow-Keong Thong, Rifhan Azwani Binti Mazlan,Sok Kun Tae,Tom Kamphans,Wolfgang Meiswinkel,Jing-Mei Li,Behnam Javanmardi,Alexej Knaus,Annette Uwineza,Cordula Knopp,Tinatin Tkemaladze,Miriam Elbracht, Larissa Mattern,Rami Abou Jamra,Clara Velmans,Vincent Strehlow, Maureen Jacob,Angela Peron,Cristina Dias,Beatriz Carvalho Nunes, Thainá Vilella, Isabel Furquim Pinheiro,Chong Ae Kim,Maria Isabel Melaragno, Hannah Weiland, Sophia Kaptain,Karolina Chwiałkowska,Miroslaw Kwasniewski, Ramy Saad,Sarah Wiethoff,Himanshu Goel, Clara Tang, Anna Hau,Tahsin Stefan Barakat, Przemysław Panek,Amira Nabil, Julia Suh,Frederik Braun,Israel Gomy,Luisa Averdunk,Ekanem Ekure,Gaber Bergant,Borut Peterlin,Claudio Graziano,Nagwa Gaboon,Moisés Fiesco-Roa,Alessandro Mauro Spinelli,Nina-Maria Wilpert,Prasit Phowthongkum,Nergis Güzel,Tobias B Haack,Rana Bitar,Andreas Tzschach,Agusti Rodriguez-Palmero,Theresa Brunet,Sabine Rudnik-Schöneborn, Silvina Noemi Contreras-Capetillo, Ava Oberlack,Carole Samango-Sprouse,Teresa Sadeghin, Margaret Olaya,Konrad Platzer,Artem Borovikov,Franziska Schnabel,Lara Heuft, Vera Herrmann,Renske Oegema,Nour Elkhateeb,Sheetal Kumar,Katalin Komlosi, Khoushoua Mohamed,Silvia Kalantari,Fabio Sirchia,Antonio F Martinez-Monseny, Matthias Höller, Louiza Toutouna, Amal Mohamed,Amaia Lasa-Aranzasti, John A Sayer,Nadja Ehmke,Magdalena Danyel,Henrike Sczakiel,Sarina Schwartzmann,Felix Boschann,Max Zhao,Ronja Adam, Lara Einicke,Denise Horn,Kee Seang Chew,Choy Chen Kam,Miray Karakoyun,Ben Pode-Shakked,Aviva Eliyahu,Rachel Rock,Teresa Carrion,Odelia Chorin,Yuri A Zarate, Marcelo Martinez Conti,Mert Karakaya,Moon Ley Tung,Bharatendu Chandra,Arjan Bouman,Aime Lumaka,Naveed Wasif,Marwan Shinawi,Patrick R Blackburn,Tianyun Wang, Tim Niehues,Axel Schmidt, Regina Rita Roth,Dagmar Wieczorek, Ping Hu,Rebekah L Waikel,Suzanna E Ledgister Hanchard,Gehad Elmakkawy,Sylvia Safwat,Frédéric Ebstein,Elke Krüger,Sébastien Küry,Stéphane Bézieau,Annabelle Arlt,Eric Olinger,Felix Marbach, Dong Li,Lucie Dupuis,Roberto Mendoza-Londono,Sofia Douzgou Houge,Denisa Weis,Brian Hon-Yin Chung,Christopher C Y Mak,Hülya Kayserili,Nursel Elcioglu,Ayca Aykut, Peli Özlem Şimşek-Kiper,Nina Bögershausen,Bernd Wollnik,Heidi Beate Bentzen,Ingo Kurth,Christian Netzer,Aleksandra Jezela-Stanek,Koen Devriendt,Karen W Gripp,Martin Mücke,Alain Verloes,Christian P Schaaf,Christoffer Nellåker,Benjamin D Solomon,Markus M Nöthen,Ebtesam Abdalla,Gholson J Lyon,Peter M Krawitz,Tzung-Chien Hsieh
Research square (2024)
引用3浏览0WOS引用
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Complex Structural Variation and Nonsense Variantin Transcausevps50-Related Disorder
Laura Hecher,Florian Kraft,Matthias Begemann, Jürgen Herwig, Eva Lausberg, Georg Hillebrand,Alexander E. Volk,Ingo Kurth,Kerstin Kutsche
Journal of medical geneticspp.jmg-109983, (2024)
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Genetic Landscape of Congenital Insensitivity to Pain and Hereditary Sensory and Autonomic Neuropathies
Annette Lischka,Katja Eggermann,Christopher J. Record,Maike F. Dohrn,Petra Lassuthova,Florian Kraft,Matthias Begemann,Daniela Dey,Thomas Eggermann,Danique Beijer,Jana Soukalova,Matilde Laura,Alexander M. Rossor,Radim Mazanec,Jonas Van Lent,Pedro J. Tomaselli,Martin Ungelenk, Karlien Y. Debus,Shawna M. E. Feely,Dieter Glaeser,Sujatha Jagadeesh,Madelena Martin, Geeta M. Govindaraj,Pratibha Singhi, Revanth Baineni,Niranjan Biswal,Marisol Ibarra-Ramirez,Maryse Bonduelle,Burkhard Gess, Juan Romero Sanchez,Renu Suthar,Vrajesh Udani,Atchayaram Nalini,Gopikrishnan Unnikrishnan,Wilson Marques Junior,Sandra Mercier,Vincent Procaccio,Celine Bris,Beena Suresh,Vaishnavi Reddy,Mariola Skorupinska,Nathalie Bonello-Palot,Fanny Mochel, Georg Dahl, Karthika Sasidharan,Fiji M. Devassikutty,Sheela Nampoothiri,Maria J. Rodovalho Doriqui,Wolfgang Mueller-Felber,Katharina Vill,Tobias B. Haack,Andreas Dufke,Michael Abele,Rolf Stucka,Saima Siddiqi,Noor Ullah,Stephanie Spranger,Deborah Chiabrando, Behiye S. Bolgul,Yesim Parman,Pavel Seeman,Angelika Lampert,Joerg B. Schulz,John N. Wood,James J. Cox,Michaela Auer-Grumbach,Vincent Timmerman,Jonathan de Winter,Andreas C. Themistocleous,Michael Shy,David L. Bennett,Jonathan Baets,Christian A. Huebner,Enrico Leipold,Stephan Zuchner,Miriam Elbracht,Arman Cakar,Jan Senderek,Thorsten Hornemann,C. Geoffrey Woods,Mary M. Reilly,Ingo Kurth
Brain（2023）
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作者统计

#Papers: 226

#Citation: 6905

H-Index: 40

G-Index: 80

Sociability: 8

Diversity: 4

Activity: 118

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