Michael Nothnagel

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 20

Top Venues

European journal of human genetics : EJHG

Nature communications

Human genetics

Molecular genetics & genomic medicine

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

Publications

Sophie A Riesmeijer, Zoha Kamali, Michael T H Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, Thomas B Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M N Werker, Dominic Furniss, Ilja Maria Nolte
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. Nature communications 15 (1) (2024)
Sophie A Riesmeijer, Zoha Kamali, Michael T H Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, Thomas B Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M N Werker, Dominic Furniss, Ilja Maria Nolte
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. Nature communications 15 (1) (2024)
Sophie A Riesmeijer, Zoha Kamali, Michael T H Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, Thomas B Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M N Werker, Dominic Furniss, Ilja Maria Nolte
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. Nature communications 15 (1) (2024)
Sophie A Riesmeijer, Zoha Kamali, Michael T H Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, Thomas B Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M N Werker, Dominic Furniss, Ilja Maria Nolte
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease. Nature communications 15 (1) (2024)
Lynn Khellaf, Arwin Ralf, Khanh Toan Nguyen, Manfred Kayser, Michael Nothnagel
SMapper: visualizing spatial prevalence data of all types, including sparse and incomplete datasets. Bioinformatics advances 3 (1) (2023)
Nina Ishorst, Leonie Henschel, Frederic Thieme, Dmitriy Drichel, Sugirthan Sivalingam, Sarah L Mehrem, Ariane C Fechtner, Julia Fazaal, Julia Welzenbach, André Heimbach, Carlo Maj, Oleg Borisov, Jonas Hausen, Ruth Raff, Alexander Hoischen, Michael Dixon, Alvaro Rada-Iglesias, Michaela Bartusel, Augusto Rojas-Martinez, Khalid Aldhorae, Bert Braumann, Teresa Kruse, Christian Kirschneck, Gerrit Spanier, Heiko Reutter, Stefanie Nowak, Lina Gölz, Michael Knapp, Andreas Buness, Peter Krawitz, Markus M Nöthen, Michael Nothnagel, Tim Becker, Kerstin U Ludwig, Elisabeth Mangold
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Molecular genetics & genomic medicine (2022)
Oluyomi M Adesoji, Herbert Schulz, Patrick May, Roland Krause, Holger Lerche, Michael Nothnagel, null null
Benchmarking of univariate pleiotropy detection methods applied to epilepsy. Human mutation 43 (9) (2022)
Michael Nothnagel, Guangyao Fan, Fei Guo, Yongfeng He, Yiping Hou, Shengping Hu, Jiang Huang, Xianhua Jiang, Wook Kim, Kicheol Kim, Chengtao Li, Hui Li, Liming Li, Shilin Li, Zhao Li, Weibo Liang, Chao Liu, Di Lu, Haibo Luo, Shengjie Nie, Meisen Shi, Hongyu Sun, Jianpin Tang, Lei Wang, Chuan-Chao Wang, Dan Wang, Shao-Qing Wen, Hongyan Wu, Weiwei Wu, Jiaxin Xing, Jiangwei Yan, Shi Yan, Hongbing Yao, Yi Ye, Libing Yun, Zhaoshu Zeng, Lagabaiyila Zha, Suhua Zhang, Xiufen Zheng, Sascha Willuweit, Lutz Roewer
Retraction Note to: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes. Human genetics (2021)
Marzieh Mohseni, Mojgan Babanejad, Kevin T Booth, Payman Jamali, Khadijeh Jalalvand, Behzad Davarnia, Fariba Ardalani, Atefeh Khoshaeen, Sanaz Arzhangi, Fatemeh Ghodratpour, Maryam Beheshtian, Faezeh Jahanshad, Hasan Otukesh, Fatemeh Bahrami, Seyed Morteza Seifati, Niloofar Bazazzadegan, Farkhonde Habibi, Hanieh Behravan, Sepide Mirzaei, Fatemeh Keshavarzi, Nooshin Nikzat, Zohreh Mehrjoo, Holger Thiele, Michael Nothnagel, Hela Azaiez, Richard J H Smith, Kimia Kahrizi, Hossein Najmabadi
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clinical genetics 100 (1) (2021)
Michael Nothnagel
Correction to: Towards a fine-scale picture of European genetic diversity. European journal of human genetics : EJHG (2021)
George Kanoungi, Michael Nothnagel, Tim Becker, Dmitriy Drichel
The exhaustive genomic scan approach, with an application to rare-variant association analysis. European journal of human genetics : EJHG 28 (9) (2020)
Michael Nothnagel
Towards a fine-scale picture of European genetic diversity. European journal of human genetics : EJHG 28 (7) (2020)
Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi, Michael Nothnagel
Distinct genetic variation and heterogeneity of the Iranian population. PLoS genetics 15 (9) (2019)
Simone Lipinski, Britt-Sabina Petersen, Matthias Barann, Agnes Piecyk, Florian Tran, Gabriele Mayr, Marlene Jentzsch, Konrad Aden, Stephanie T Stengel, Ulrich C Klostermeier, Vrunda Sheth, David Ellinghaus, Tobias Rausch, Jan O Korbel, Michael Nothnagel, Michael Krawczak, Christian Gilissen, Joris A Veltman, Michael J Forster, Peter Forster, Clarence C Lee, Annette Fritscher-Ravens, Stefan Schreiber, Andre Franke, Philip C Rosenstiel
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2. Cold Spring Harbor molecular case studies 5 (1) (2019)
Ben Krause-Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini, Dorthe Dangvard Pedersen, Sabin-Christin Kornell, Dmitriy Drichel, Marion Bonazzi, Lena Möbus, Peter Tarp, Julian Susat, Esther Bosse, Beatrix Willburger, Alexander H Schmidt, Jürgen Sauter, Andre Franke, Michael Wittig, Amke Caliebe, Michael Nothnagel, Stefan Schreiber, Jesper L Boldsen, Tobias L Lenz, Almut Nebel
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans. Nature communications 9 (1) (2018)
George Kanoungi, Michael Nothnagel
Pathway-induced allelic spectra of diseases in the presence of strong genetic effects. Human genetics 137 (3) (2018)
Reza Asadollahi, Justin E Strauss, Martin Zenker, Oliver Beuing, Simon Edvardson, Orly Elpeleg, Tim M Strom, Pascal Joset, Dunja Niedrist, Christine Otte, Beatrice Oneda, Paranchai Boonsawat, Silvia Azzarello-Burri, Deborah Bartholdi, Michael Papik, Markus Zweier, Cordula Haas, Arif Bülent Ekici, Alessandra Baumer, Eugen Boltshauser, Katharina Steindl, Michael Nothnagel, Albert Schinzel, Esther T Stoeckli, Anita Rauch
Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling. European journal of human genetics : EJHG 26 (2) (2018)
George Kanoungi, Peter Nürnberg, Michael Nothnagel
Securing the use of existing sample collections for future human genetic research. European journal of human genetics : EJHG 25 (5) (2017)
Michael Nothnagel, Guangyao Fan, Fei Guo, Yongfeng He, Yiping Hou, Shengping Hu, Jiang Huang, Xianhua Jiang, Wook Kim, Kicheol Kim, Chengtao Li, Hui Li, Liming Li, Shilin Li, Zhao Li, Weibo Liang, Chao Liu, Di Lu, Haibo Luo, Shengjie Nie, Meisen Shi, Hongyu Sun, Jianpin Tang, Lei Wang, Chuan-Chao Wang, Dan Wang, Shao-Qing Wen, Hongyan Wu, Weiwei Wu, Jiaxin Xing, Jiangwei Yan, Shi Yan, Hongbing Yao, Yi Ye, Libing Yun, Zhaoshu Zeng, Lagabaiyila Zha, Suhua Zhang, Xiufen Zheng, Sascha Willuweit, Lutz Roewer
Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes. Human genetics 136 (5) (2017)
Eva Seemanova, Raymonda Varon, Jan Vejvalka, Petr Jarolím, Pavel Seeman, Krystyna H Chrzanowska, Martin Digweed, Igor Resnick, Ivo Kremensky, Kathrin Saar, Katrin Hoffmann, Véronique Dutrannoy, Mohsen Karbasiyan, Mehdi Ghani, Ivo Barić, Mustafa Tekin, Peter Kovacs, Michael Krawczak, André Reis, Karl Sperling, Michael Nothnagel
The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? PloS one 11 (12) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Michael Nothnagel