Maja Hempel

6.4k total citations
58 papers, 855 citations indexed

About

Maja Hempel is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Maja Hempel has authored 58 papers receiving a total of 855 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 33 papers in Molecular Biology and 8 papers in Clinical Biochemistry. Recurrent topics in Maja Hempel's work include Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Maja Hempel is often cited by papers focused on Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Maja Hempel collaborates with scholars based in Germany, United States and Netherlands. Maja Hempel's co-authors include Tim M. Strom, Jonas Denecke, Davor Lessel, Kerstin Kutsche, Tatjana Bierhals, Katja Kloth, Thomas Meitinger, Jessika Johannsen, Tobias B. Haack and Holger Prokisch and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Maja Hempel

53 papers receiving 830 citations

Peers

Countries citing papers authored by Maja Hempel

Since Specialization

Citations

This map shows the geographic impact of Maja Hempel'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 Maja Hempel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maja Hempel more than expected).

Fields of papers citing papers by Maja Hempel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maja Hempel. 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 Maja Hempel. The network helps show where Maja Hempel may publish in the future.

Co-authorship network of co-authors of Maja Hempel

This figure shows the co-authorship network connecting the top 25 collaborators of Maja Hempel. A scholar is included among the top collaborators of Maja Hempel 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 Maja Hempel. Maja Hempel 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	Homozygous DBX1 Nonsense Variant in a Case of Atypical Congenital Central Hypoventilation 2025 ·Neurology Genetics ·Amelie T. van der Ven, Maja Hempel, Chris G. Kruse, Martin Blohm, (unknown), Christian Kubisch, Davor Lessel	0
2	Novel biallelic COL25A1 variants broaden the clinical spectrum from congenital cranial dysinnervation disorders to fetal lethal phenotypes 2025 ·European Journal of Human Genetics ·Frederike L. Harms, Christian Müller, Fanny Kortüm, Maja Hempel, Malik Alawi, Maha S. Zaki, (unknown), Mohamed S. Abdel‐Hamid, Lama AlAbdi, Fowzan S. Alkuraya, Wesam Kurdi, (unknown), Marta Spodenkiewicz, (unknown), Klaus Dieterich, Sujatha Jagadeesh, (unknown), Katta M. Girisha, (unknown)	0
3	Phenotypical and Genotypical Expansion of Autosomal‐Dominant KDM1A ‐Related Neurodevelopmental Disorder Spectrum: A Case Report 2025 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Lilian Kaufmann, Katrin Hinderhofer, Christian P. Schaaf, Markus Ries, Maja Hempel	0
4	Expanding the phenotypic and biochemical spectrum of NDUFAF3-related mitochondrial disease 2023 ·Molecular Genetics and Metabolism ·Amelie T. van der Ven, Alfredo Cabrera‐Orefice, (unknown), René G. Feichtinger, Konstantinos Tsiakas, Deike Weiss, Tatjana Bierhals, (unknown), Holger Prokisch, Robert Kopajtich, René Santer, Johannes A. Mayr, Maja Hempel, Ilka Wittig	4
5	Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy 2022 ·Brain ·Shehrazade Dahimène, (unknown), (unknown), (unknown), (unknown), Davor Lessel, Kjara S Pilch, Ivan Kadurin, Wendy S. Pratt, Igor B. Zhulin, Hongzheng Dai, Maja Hempel, Maura Ruzhnikov, Kerstin Kutsche, Annette Dolphin	29
6	Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies 2022 ·European Journal of Human Genetics ·Miriam S. Reuter, Michael Zech, Maja Hempel, Janine Altmüller, Tracy Heung, (unknown), René Santer, Hölger Thiele, Brett Trost, Christian Kubisch, Stephen W. Scherer, Sabine Rudnik‐Schöneborn, Anne S. Bassett, Davor Lessel	3
7	Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation 2021 ·Brain ·(unknown), Guoliang Chai, (unknown), Frederike L. Harms, Christian Casar, (unknown), Malik Alawi, Ghada M. H. Abdel‐Salam, Maha S. Zaki, (unknown), Xiaoxu Yang, Valentina Stanley, Maja Hempel, Joseph G. Gleeson, (unknown)	11
8	Fatal COVID-19 in a Child with Persistence of SARS-CoV-2 Despite Extensive Multidisciplinary Treatment: A Case Report 2021 ·Children ·(unknown), (unknown), Peter Lasch, Daniel Biermann, Maja Hempel, Marc Lütgehetmann, Susanne Pfefferle, Jochen Herrmann, André Rüffer, Konrad Reinshagen, Rainer Kozlik‐Feldmann, Anna Gieras, Inga Kniep, Jun Oh, Dominique Singer, (unknown), Robin Kobbe	5
9	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males 2021 ·Human Genetics ·Hans‐Jürgen Kreienkamp, Matias Wagner, Heike Weigand, (unknown), Marie McDonald, Boris Keren, Cyril Mignot, Julie Gauthier, (unknown), Jacques L. Michaud, (unknown), Rosemarie Smith, Ulrike Löbel, Maja Hempel, Christian Kubisch, Jonas Denecke, Philippe M. Campeau, Jennifer Bain, Davor Lessel	13
10	Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort 2021 ·Clinical Genetics ·Amelie T. van der Ven, Jessika Johannsen, Fanny Kortüm, Matias Wagner, Konstantinos Tsiakas, Tatjana Bierhals, Davor Lessel, Theresia Herget, Katja Kloth, Jasmin Lisfeld, (unknown), Nadia Obi, Saskia B. Wortmann, Holger Prokisch, Christian Kubisch, Jonas Denecke, René Santer, Maja Hempel	8
11	Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia 2021 ·Annals of Neurology ·Claudia Schob, Maja Hempel, Dana Šafka Brožková, (unknown), Soo Yeon Kim, Nurit Assia Batzir, Naama Orenstein, Tatjana Bierhals, Jessika Johannsen, (unknown), Jong‐Hee Chae, Pavel Seeman, (unknown), Fang Fang, Christian Kubisch, Stefan Kindler, Jonas Denecke	6
12	POLR3A variants with striatal involvement and extrapyramidal movement disorder 2020 ·Neurogenetics ·Inga Harting, (unknown), Ingeborg Krägeloh‐Mann, Annette Bley, Maja Hempel, Tatjana Bierhals, Stephanie Karch, Ute Moog, Geneviève Bernard, Richard J. Huntsman, Rosalina M.L. van Spaendonk, Maaike Vreeburg, Agustí Rodríguez‐Palmero, Aurora Pujol, Marjo S. van der Knaap, Petra J. W. Pouwels, Nicole I. Wolf	26
13	Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population 2020 ·Journal of Human Genetics ·Carolina Sismani, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Athina Theodosiou, Maria Syrrou, Sigrid Fuchs, Maja Hempel, Dagmar Huhle, Thomas Liehr, Monika Ziegler, (unknown), Voula Velissariou	9
14	A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions 2020 ·PLoS Genetics ·(unknown), (unknown), Tatjana Bierhals, Marta Campiglio, Jessika Johannsen, Gerald J. Obermair, Maja Hempel, Bernhard E. Flucher, Kerstin Kutsche	26
15	Recurrent acute liver failure in alanyl-tRNA synthetase-1 (AARS1) deficiency 2020 ·Molecular Genetics and Metabolism Reports ·(unknown), Florian Brinkert, Desirée E.C. Smith, Holger Prokisch, Maja Hempel, René Santer	4
16	16p13.11 microdeletion uncovers loss‐of‐function of a MYH11 missense variant in a patient with megacystis‐microcolon‐intestinal‐hypoperistalsis syndrome 2019 ·Clinical Genetics ·Katja Kloth, (unknown), (unknown), Doris Steinemann, Brigitte Pabst, Birgit Lorenz, Ronald Simon, (unknown), Maja Hempel, Georg Rosenberger	20
17	Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis 2019 ·Journal of Clinical Investigation ·Martin D. Burkhalter, Arthi Sridhar, (unknown), (unknown), (unknown), Cornelia Donow, (unknown), Maja Hempel, Paul Walther, Petra Pennekamp, Heymut Omran, Susana S. Lopes, Stephanie M. Ware, Melanie Philipp	42
18	Mutations in PIGU Impair the Function of the GPI Transamidase Complex, Causing Severe Intellectual Disability, Epilepsy, and Brain Anomalies 2019 ·The American Journal of Human Genetics ·Alexej Knaus, Fanny Kortüm, Tjitske Kleefstra, Asbjørg Stray‐Pedersen, (unknown), Yoshiko Murakami, Thorsten Gerstner, Hans van Bokhoven, Zafar Iqbal, Denise Horn, Taroh Kinoshita, Maja Hempel, Peter Krawitz	35
19	Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1 2017 ·American Journal of Medical Genetics Part A ·Edith Said, Jessica X. Chong, Maja Hempel, Jonas Denecke, P Soler, Tim M. Strom, Deborah A. Nickerson, Christian Kubisch, Michael J. Bamshad, Davor Lessel	8
20	Rare Syndromes Associated with Infertility 2009 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·Maja Hempel, Tina Buchholz	2

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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