Ohcanbohtosat - Henrike Heyne
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Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events Dahkki Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, Reetta Kälviäinen, Mark J. Daly
Almmustuhtton 2024Artigo -
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Widely Used Commercial ELISA Does Not Detect Precursor of Haptoglobin2, but Recognizes Properdin as a Potential Second Member of the Zonulin Family Dahkki Lucas Scheffler, Alyce Crane, Henrike Heyne, Anke Tönjes, Dorit Schleinitz, Christian Ihling, Michael Stümvoll, Rachel Freire, Maria Fiorentino, Alessio Fasano, Péter Kovács, John T. Heiker
Almmustuhtton 2018Artigo -
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Gene variant effects across sodium channelopathies predict function and guide precision therapy Dahkki Andreas Brunklaus, Tony Feng, Tobias Brünger, Eduardo Pérez‐Palma, Henrike Heyne, Emma Matthews, Christopher Semsarian, Joseph D. Symonds, Sameer M. Zuberi, Dennis Lal, Stéphanie Schorge
Almmustuhtton 2022Revisão -
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Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity Dahkki Teng Hiang Heng, Klaudia Walter, Qin Huang, Juha Karjalainen, Mark J. Daly, Henrike Heyne, Daniel Malawsky, Georgios Kalantzis, Sarah Finer, David A. van Heel, Hilary C. Martin
Almmustuhtton 2025Artigo -
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Identification of pathogenic variant enriched regions across genes and gene families Dahkki Eduardo Pérez‐Palma, Patrick May, Sumaiya Iqbal, Lisa‐Marie Niestroj, Juanjiangmeng Du, Henrike Heyne, Jessica A. Castrillon, Anne O’Donnell‐Luria, Peter Nürnberg, Aarno Palotie, Mark J. Daly, Jessica C. Lal
Almmustuhtton 2019Artigo -
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Adipose tissue derived bacteria are associated with inflammation in obesity and type 2 diabetes Dahkki Lucas Massier, Rima Chakaroun, Shirin Tabei, Alyce Crane, K Didt, Jörg Fallmann, Martin von Bergen�, Sven‐Bastiaan Haange, Henrike Heyne, Michael Stümvoll, Martin Gericke, Arne Dietrich, Matthias Blüher, Niculina Musat, Péter Kovács
Almmustuhtton 2020Artigo -
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Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression Dahkki Henrike Heyne, Susann Lautenschläger, Ronald M. Nelson, François Besnier, Maxime Rotival, Alex Cagan, R. V. Kozhemyakina, Irina Z. Plyusnina, Lyudmila N. Trut, Örjan Carlborg, Enrico Petretto, Leonid Kruglyak, Svante Pääbo, Torsten Schöneberg, Frank W. Albert
Almmustuhtton 2014Artigo -
9
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy Dahkki Henrike Heyne, Mykyta Artomov, Florian Battke, Claudia Bianchini, Douglas R. Smith, Nora Liebmann, Vasisht Tadigotla, Christine M. Stanley, Dennis Lal, Heidi L. Rehm, Holger Lerche, Mark J. Daly, Ingo Helbig, Saskia Biskup, Yvonne G. Weber, Johannes R. Lemke
Almmustuhtton 2019Artigo -
10
Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants Dahkki Sumaiya Iqbal, Eduardo Pérez‐Palma, Jakob Berg Jespersen, Patrick May, David Hoksza, Henrike Heyne, Shehab Ahmed, Zaara T. Rifat, M. Sohel Rahman, Kasper Lage, Aarno Palotie, Jeffrey R. Cottrell, Florence F. Wagner, Mark J. Daly, Arthur J. Campbell, Dennis Lal
Almmustuhtton 2020Artigo -
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Predicting functional effects of missense variants in voltage-gated sodium and calcium channels Dahkki Henrike Heyne, David Báez-Nieto, Sumaiya Iqbal, Duncan S. Palmer, Andreas Brunklaus, Patrick May, Katrine M. Johannesen, Stephan Lauxmann, Johannes R. Lemke, Rikke S. Møller, Eduardo Pérez‐Palma, Ute I. Scholl, Steffen Syrbe, Holger Lerche, Dennis Lal, Arthur J. Campbell, Hao‐Ran Wang, Jen Q. Pan, Mark J. Daly
Almmustuhtton 2020Artigo -
12
Neolithic and medieval virus genomes reveal complex evolution of hepatitis B Dahkki Ben Krause‐Kyora, Julian Susat, Felix M. Key, Denise Kühnert, Esther Bosse, Alexander Immel, Christoph Rinne, Sabin-Christin Kornell, Diego Yepes, Sören Franzenburg, Henrike Heyne, Thomas Meier, Sandra Lösch, Harald Meller, Susanne Friederich, Nicole Nicklisch, Kurt W. Alt, Stefan Schreiber, Andreas Tholey, Alexander Herbig, Almut Nebel, Johannes Krause
Almmustuhtton 2018Artigo -
13
Paternal-age-related de novo mutations and risk for five disorders Dahkki Jacob Taylor, Jean-Christophe Debost, Sarah U. Morton, Emilie M. Wigdor, Henrike Heyne, Dennis Lal, Daniel P. Howrigan, Alex Bloemendal, Janne Tidselbak Larsen, Jack A. Kosmicki, Daniel J. Weiner, Jason Homsy, Jonathan G. Seidman, Christine E. Seidman, Esben Agerbo, John J. McGrath, Preben Bo Mortensen, Liselotte Petersen, Mark J. Daly, Elise Robinson
Almmustuhtton 2019Artigo -
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Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA Dahkki Adam B. Rohrlach, Maïté Rivollat, María Paz de Miguel Ibáñez, Ulla Moilanen, Anne-Mari Liira, João C. Teixeira, Xavier Roca‐Rada, Javier Armendáriz-Martija, Kamen Boyadzhiev, Yavor Boyadzhiev, Bastien Llamas, Anthi Tiliakou, Angela Mötsch, Jonathan Tuke, Eleni-Anna Prevedorou, Naya Polychronakou-Sgouritsa, Jane E. Buikstra, Päivi Onkamo, Philipp W. Stockhammer, Henrike Heyne, Johannes R. Lemke, Roberto Risch, Stephan Schiffels, Johannes Krause, Wolfgang Haak, Kay Prüfer
Almmustuhtton 2024Artigo -
15
De novo variants in neurodevelopmental disorders with epilepsy Dahkki Henrike Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Çağlayan, Dana Craiu, Peter De Jonghe, Renzo Guerrini, Katherine L. Helbig, Bobby P.C. Koeleman, Jack A. Kosmicki, Tarja Linnankivi, Patrick May, Hiltrud Muhle, Rikke S. Møller, Bernd A. Neubauer, Aarno Palotie, Manuela Pendziwiat, Pasquale Striano, Sha Tang, Sitao Wu, Annapurna Poduri, Yvonne G. Weber, Sarah Weckhuysen, Sanjay M. Sisodiya, Mark J. Daly, Ingo Helbig, Dennis Lal, Johannes R. Lemke
Almmustuhtton 2018Artigo -
16
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk Dahkki Bradley Jermy, Kristi Läll, Brooke N. Wolford, Ying Wang, Kristina Zguro, Yipeng Cheng, Masahiro Kanai, Stavroula Kanoni, Zhiyu Yang, Tuomo Hartonen, Remo Monti, Julian Wanner, Omar Youssef, Christoph Lippert, David A. van Heel, Yukinori Okada, Daniel L. McCartney, Caroline Hayward, Riccardo E. Marioni, Simone Furini, Alessandra Renieri, Alicia R. Martin, Benjamin M. Neale, Kristian Hveem, Reedik Mägi, Aarno Palotie, Henrike Heyne, Nina Mars, Andrea Ganna, Samuli Ripatti
Almmustuhtton 2024Artigo -
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Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery Dahkki J German, Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit, Jiwoo Lee, Josephine H. Li, Adrian Janucik, Yi Ding, Akintunde O. Akinkuolie, Henrike Heyne, Andrea Eoli, Chadi Saad, Yasser Al‐Sarraj, Rania G. Abdel‐latif, Shaban Mohammed, Moza Al Hail, Alexandra Barry, Zhe Wang, Tatiana Cajuso, Andrea Corbetta, Pradeep Natarajan, Samuli Ripatti, Anthony Philippakis, Łukasz Szczerbiński, Bogdan Paşaniuc, Zoltán Kutalik, Hamdi Mbarek, Ruth J. F. Loos, Uku Vainik, Andrea Ganna
Almmustuhtton 2025Artigo -
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Biological concepts in human sodium channel epilepsies and their relevance in clinical practice Dahkki Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, Ismael Ghanty, Katrine M. Johannesen, Christina Fenger, Stéphanie Schorge, David Báez-Nieto, Hao‐Ran Wang, Andrew S. Allen, Jen Q. Pan, Holger Lerche, Henrike Heyne, Joseph D. Symonds, Sameer M. Zuberi, Stephan Sanders, Beth Rosen Sheidley, Dana Craiu, Heather E. Olson, Sarah Weckhuysen, Peter M. DeJonge, Ingo Helbig, Hilde Van Esch, Tiffany Busa, M. Milh, Bertrand Isidor, Christel Depienne, Annapurna Poduri, Arthur J. Campbell, Jordane Dimidschstein, Rikke S. Møller, Dennis Lal
Almmustuhtton 2020Artigo -
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The origin and legacy of the Etruscans through a 2000-year archeogenomic time transect Dahkki Cosimo Posth, Valentina Zaro, Maria A. Spyrou, Stefania Vai, Guido Alberto Gnecchi‐Ruscone, Alessandra Modi, Alexander Peltzer, Angela Mötsch, Kathrin Nägele, Åshild J. Vågene, Elizabeth A. Nelson, Rita Radzevičiūtė, Cäcilia Freund, Lorenzo M. Bondioli, Luca Cappuccini, H. Frenzel, Elsa Pacciani, Francesco Boschin, Giulia Capecchi, Ivan Martini, Adriana Moroni, Stefano Ricci, Alessandra Sperduti, Maria Angela Turchetti, Alessandro Riga, M. Zavattaro, Andrea Zifferero, Henrike Heyne, Eva Fernández‐Domínguez, Guus Kroonen, Michael McCormick, Wolfgang Haak, Martina Lari, Guido Barbujani, Luca Bondioli, Kirsten I. Bos, David Caramelli, Johannes Krause
Almmustuhtton 2021Artigo -
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Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy Dahkki Steffen Syrbe, Frederike L. Harms, Elena Parrini, Martino Montomoli, Ulrike Mütze, Katherine L. Helbig, Tilman Polster, Beate Albrecht, Ulrich Bernbeck, Ellen van Binsbergen, Saskia Biskup, Lydie Bürglen, Jonas Denecke, Bénédicte Héron, Henrike Heyne, Georg F. Hoffmann, Frauke Hornemann, Takeshi Matsushige, Ryuki Matsuura, Mitsuhiro Kato, Georg Christoph Korenke, Alma Kuechler, Constanze Lämmer, Andreas Merkenschlager, Cyril Mignot, Susanne Ruf, Mitsuko Nakashima, Hirotomo Saitsu, Hannah Stamberger, Tiziana Pisano, Jun Tohyama, Sarah Weckhuysen, Wendy Werckx, Julia Wickert, Francesco Mari, Nienke E. Verbeek, Rikke S. Møller, Bobby P.C. Koeleman, Naomichi Matsumoto, William B. Dobyns, Domenica Battaglia, Johannes R. Lemke, Kerstin Kutsche, Renzo Guerrini
Almmustuhtton 2017Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Gene
Genetics
Medicine
Phenotype
Epilepsy
Internal medicine
Neuroscience
Missense mutation
Computational biology
Population
Demography
Genome
Genotype
Psychiatry
Sociology
Bioinformatics
Single-nucleotide polymorphism
Biobank
Chemistry
Disease
Environmental health
Mutation
Allele
Candidate gene
Copy-number variation
Encephalopathy
Evolutionary biology
Exome
Exome sequencing