Henrike Heyne

12.5k total citations
23 papers, 715 citations indexed

About

Henrike Heyne is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Henrike Heyne has authored 23 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Henrike Heyne's work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Associations and Epidemiology (4 papers). Henrike Heyne is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Associations and Epidemiology (4 papers). Henrike Heyne collaborates with scholars based in Germany, United States and Finland. Henrike Heyne's co-authors include Mark J. Daly, Dennis Lal, Michael Stümvoll, Péter Kovács, Eduardo Pérez‐Palma, Patrick May, Sumaiya Iqbal, Aarno Palotie, Anke Tönjes and Matthias Blüher and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Henrike Heyne

21 papers receiving 699 citations

Peers

Countries citing papers authored by Henrike Heyne

Since Specialization

Citations

This map shows the geographic impact of Henrike Heyne's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Henrike Heyne with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Henrike Heyne more than expected).

Fields of papers citing papers by Henrike Heyne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Henrike Heyne. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Henrike Heyne. The network helps show where Henrike Heyne may publish in the future.

Co-authorship network of co-authors of Henrike Heyne

This figure shows the co-authorship network connecting the top 25 collaborators of Henrike Heyne. A scholar is included among the top collaborators of Henrike Heyne based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Henrike Heyne. Henrike Heyne is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity 2025 ·The American Journal of Human Genetics ·(unknown), Klaudia Walter, Qin Huang, Juha Karjalainen, Mark J. Daly, Henrike Heyne, Daniel Malawsky, (unknown), Sarah Finer, David A. van Heel, Hilary C. Martin	0
2	A clustering approach to improve our understanding of the genetic and phenotypic complexity of chronic kidney disease 2024 ·Scientific Reports ·(unknown), (unknown), Claudia Schurmann, Girish N. Nadkarni, Henrike Heyne, Erwin P. Böttinger	2
3	Inherited infertility: Mapping loci associated with impaired female reproduction 2024 ·The American Journal of Human Genetics ·Sanni Ruotsalainen, Juha Karjalainen, Mitja Kurki, Elisa Lahtela, Matti Pirinen, Juha Riikonen, Jarmo Ritari, (unknown), Jukka Partanen, Hannele Laivuori, Aarno Palotie, Henrike Heyne, (unknown), Elisabeth Widén	1
4	Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events 2024 ·Nature Communications ·Henrike Heyne, (unknown), (unknown), (unknown), Reedik Mägi, Aarno Palotie, (unknown), Reetta Kälviäinen, Mark J. Daly	8
5	Mono- and biallelic variant effects on disease at biobank scale 2023 ·Nature ·Henrike Heyne, Juha Karjalainen, Konrad J. Karczewski, Susanna Lemmelä, Wei Zhou, (unknown), Aki S. Havulinna, Mitja Kurki, Heidi L. Rehm, Aarno Palotie, Mark J. Daly	37
6	Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population 2023 ·The American Journal of Human Genetics ·(unknown), (unknown), Siwei Chen, (unknown), (unknown), Antje Garten, Saskia Biskup, Florian Battke, Dennis Lal, Henrike Heyne, Konrad Platzer, (unknown), Johannes R. Lemke, Diana Le Duc	0
7	Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort 2021 ·Brain ·David Báez-Nieto, Andrew S. Allen, (unknown), Lingling Yang, Nikita Budnik, Amaury Pupo, (unknown), Giulio Genovese, Maofu Liao, Eduardo Pérez‐Palma, Henrike Heyne, Dennis Lal, Diane Lipscombe, Jen Q. Pan	21
8	A novel compound heterozygous leptin receptor mutation causes more severe obesity than in Lepr mice 2021 ·Journal of Lipid Research ·C Berger, Henrike Heyne, (unknown), (unknown), Corinna Höfling, Esther Guiu‐Jurado, (unknown), Steffen Roßner, Michael Dannemann, Janet Kelso, Péter Kovács, Matthias Blüher, Nora Klöting	6
9	Genetically programmed changes in transcription of the novel progranulin regulator 2020 ·Journal of Molecular Medicine ·Maria Keller, Claudia Gebhardt, (unknown), Dorit Schleinitz, Henrike Heyne, Markus Scholz, Michael Stümvoll, Yvonne Böttcher, Anke Tönjes, Péter Kovács	5
10	Adipose tissue derived bacteria are associated with inflammation in obesity and type 2 diabetes 2020 ·Gut ·Lucas Massier, Rima Chakaroun, (unknown), (unknown), (unknown), Jörg Fallmann, Martin von Bergen�, Sven‐Bastiaan Haange, Henrike Heyne, Michael Stümvoll, Martin Gericke, Arne Dietrich, Matthias Blüher, Niculina Musat, Péter Kovács	134
11	Predicting functional effects of missense variants in voltage-gated sodium and calcium channels 2020 ·Science Translational Medicine ·Henrike Heyne, David Báez-Nieto, Sumaiya Iqbal, Duncan S. Palmer, Andreas Brunklaus, Patrick May, (unknown), 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, (unknown), Jen Q. Pan, Mark J. Daly	80
12	MISCAST: MIssense variant to protein StruCture Analysis web SuiTe 2020 ·Nucleic Acids Research ·Sumaiya Iqbal, David Hoksza, Eduardo Pérez‐Palma, Patrick May, Jakob Berg Jespersen, (unknown), (unknown), Henrike Heyne, M. Sohel Rahman, Jeffrey R. Cottrell, Florence F. Wagner, Mark J. Daly, Arthur J. Campbell, Dennis Lal	13
13	Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants 2020 ·Proceedings of the National Academy of Sciences ·Sumaiya Iqbal, Eduardo Pérez‐Palma, Jakob Berg Jespersen, Patrick May, David Hoksza, Henrike Heyne, (unknown), (unknown), M. Sohel Rahman, Kasper Lage, Aarno Palotie, Jeffrey R. Cottrell, Florence F. Wagner, Mark J. Daly, Arthur J. Campbell, Dennis Lal	58
14	Paternal-age-related de novo mutations and risk for five disorders 2019 ·Nature Communications ·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	61
15	Identification of pathogenic variant enriched regions across genes and gene families 2019 ·Genome Research ·Eduardo Pérez‐Palma, Patrick May, Sumaiya Iqbal, Lisa‐Marie Niestroj, (unknown), Henrike Heyne, Jessica A. Castrillon, Anne O’Donnell‐Luria, Peter Nürnberg, Aarno Palotie, Mark J. Daly, (unknown)	36
16	Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy 2019 ·Genetics in Medicine ·Henrike Heyne, Mykyta Artomov, Florian Battke, Claudia Bianchini, Douglas R. Smith, (unknown), Vasisht Tadigotla, Christine M. Stanley, Dennis Lal, Heidi L. Rehm, Holger Lerche, Mark J. Daly, Ingo Helbig, Saskia Biskup, Yvonne Weber, Johannes R. Lemke	36
17	Widely Used Commercial ELISA Does Not Detect Precursor of Haptoglobin2, but Recognizes Properdin as a Potential Second Member of the Zonulin Family 2018 ·Frontiers in Endocrinology ·(unknown), (unknown), Henrike Heyne, Anke Tönjes, Dorit Schleinitz, Christian Ihling, Michael Stümvoll, Rachel Freire, Maria Fiorentino, Alessio Fasano, Péter Kovács, John T. Heiker	107
18	Die historische Entwicklung genetischer Epilepsiediagnostik 2015 ·Zeitschrift für Epileptologie ·Henrike Heyne, Johannes R. Lemke	1
19	The spectrum of GRIN2A-associated disorders 2015 ·Max Planck Digital Library ·Vincent Strehlow, Henrike Heyne, Johannes R. Lemke	4
20	Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression 2014 ·Genetics ·Henrike Heyne, (unknown), 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	43

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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