Henrike O Heyne (H O Heyne, Henrike Heyne)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 25

Top Topics

Congenital Heart Disease

Duchenne Muscular Dystrophy

Genome Wide Association

Top Venues

Nature communications

medRxiv : the preprint server for health sciences

Proceedings of the National Academy of Sciences of the United States of America

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

Publications

Henrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, null null, null null, Reetta Kälviainen, Mark J Daly
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. Nature communications 15 (1) (2024)
Henrike O Heyne
Rare developmental disorder caused by variants in a small RNA gene. Nature 632 (8026) (2024)
Henrike O Heyne
Rare developmental disorder caused by variants in a small RNA gene. Nature (2024)
Bradley S 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, null null, null null, 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 O Heyne, Nina J Mars, Andrea Ganna, Samuli Ripatti
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Nature communications 15 (1) (2024)
Henrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, null null, null null, Reetta Kälviainen, Mark J Daly
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. Nature communications 15 (1) (2024)
Bradley S 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, null null, null null, 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 O Heyne, Nina J Mars, Andrea Ganna, Samuli Ripatti
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Nature communications 15 (1) (2024)
Henrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, null null, null null, Reetta Kälviainen, Mark J Daly
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. Nature communications 15 (1) (2024)
Bradley S 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, null null, null null, 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 O Heyne, Nina J Mars, Andrea Ganna, Samuli Ripatti
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Nature communications 15 (1) (2024)
Henrike O Heyne
Rare developmental disorder caused by variants in a small RNA gene. Nature (2024)
Henrike O Heyne
Rare developmental disorder caused by variants in a small RNA gene. Nature 632 (8026) (2024)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
A Eoli, S Ibing, Claudia Schurmann, Girish Nitin Nadkarni, Henrike O Heyne, E Böttinger
A clustering approach to improve our understanding of the genetic and phenotypic complexity of chronic kidney disease. medRxiv : the preprint server for health sciences (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, null null, Reetta Kälviainen, Mark J Daly
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. medRxiv : the preprint server for health sciences (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, J Karjalainen, Konrad J Karczewski, S M Lemmelä, Wei Zhou, null null, Aki Samuli Havulinna, M Kurki, Michael J Bamshad, Aarno Palotie, Mark J Daly
Mono- and biallelic variant effects on disease at biobank scale. Nature 613 (7944) (2023)
Henrike O Heyne, David Baez-Nieto, Sumaiya Iqbal, Duncan S Palmer, Andreas Brunklaus, Patrick May, null null, Katrine Marie Johannesen, Stephan Lauxmann, Johannes R Lemke, Rikke Steensjerre Moller, Eduardo Pérez-Palma, Ute I Scholl, Steffen Syrbe, Holger Lerche, Dennis Lal, Arthur J Campbell, Hao-Ran Wang, Jen Pan, Mark J Daly
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels. Science translational medicine 12 (556) (2021)
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 Radzeviciute, Caecilia Freund, Lorenzo M Bondioli, Luca Cappuccini, Hannah Frenzel, Elsa Pacciani, Francesco Boschin, Giulia Capecchi, Ivan Martini, Adriana Moroni, Stefano Ricci, Alessandra Sperduti, Maria Angela Turchetti, Alessandro Riga, Monica Zavattaro, Andrea Zifferero, Henrike O Heyne, Eva Fernández-Domínguez, Guus J Kroonen, Michael McCormick, Wolfgang Haak, Martina Lari, Guido Barbujani, Luca Bondioli, Kirsten I Bos, David Caramelli, Johannes Krause
The origin and legacy of the Etruscans through a 2000-year archeogenomic time transect. Science advances 7 (39) (2021)
Sumaiya Iqbal, Eduardo Pérez-Palma, Jakob B Jespersen, Patrick May, David Hoksza, Henrike O Heyne, Shehab S 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
Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants. Proceedings of the National Academy of Sciences of the United States of America 117 (45) (2020)
Henrike O Heyne, Mykyta Artomov, Florian Battke, Claudia Bianchini, Douglas R Smith, Nora Liebmann, Vasisht Tadigotla, Christine M Stanley, Dennis Lal, Michael J Bamshad, Holger Lerche, Mark J Daly, Ingo Helbig, Saskia Biskup, Yvonne G Weber, Johannes R Lemke
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)