Felix Boschann

758 total citations
21 papers, 165 citations indexed

About

Felix Boschann is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Felix Boschann has authored 21 papers receiving a total of 165 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Felix Boschann's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Felix Boschann is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Felix Boschann collaborates with scholars based in Germany, France and United Kingdom. Felix Boschann's co-authors include Christoph Melzer, Björn Fischer‐Zirnsak, Manuel Holtgrewe, Dragić Banković, Thomas Dschietzig, Veselin Mitrović, Nadja Ehmke, Dominik Seelow, Stefan Mundlos and Franz Paul Armbruster and has published in prestigious journals such as Nucleic Acids Research, Frontiers in Immunology and Epilepsia.

In The Last Decade

Felix Boschann

19 papers receiving 163 citations

Peers

Countries citing papers authored by Felix Boschann

Since Specialization

Citations

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

Fields of papers citing papers by Felix Boschann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Felix Boschann

This figure shows the co-authorship network connecting the top 25 collaborators of Felix Boschann. A scholar is included among the top collaborators of Felix Boschann 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 Felix Boschann. Felix Boschann 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	Novel Biallelic SQSTM1 Mutation Causing a Subacute‐Onset Complex Movement Disorder with Oculomotor Abnormalities 2025 ·Movement Disorders Clinical Practice ·(unknown), (unknown), Jonas Leubner, Felix Boschann, Nadja Ehmke, Christoph J. Ploner, Tina Mainka, Markus Schuelke, Andrea A. Kühn	0
2	Medulloblastoma in children with Fanconi anemia: Association with FA-D1/FA-N, SHH type and poor survival independent of treatment strategies 2024 ·Neuro-Oncology ·(unknown), Denise Obrecht, Pablo Hernáiz Driever, Axel Sauerbrey, Norbert Graf, Udo Kontny, Christian Reimann, (unknown), Uwe Kordes, Rudolf Schwarz, Tobias Obser, Felix Boschann, Ulrich Schüller, (unknown), Tobias Goschzik, Torsten Pietsch, Martin Mynarek, Stefan Rutkowski	1
3	Epilepsy as a Novel Phenotype of BPTF-Related Disorders 2024 ·Pediatric Neurology ·Alessandro Ferretti, (unknown), Kevin E. Glinton, Christina Fenger, Felix Boschann, (unknown), (unknown), Raffaella Moretti, (unknown), Daniel Tarquinio, Francesca Furia, Pasquale Parisi, Guido Rubboli, Orrin Devinsky, Cyril Mignot, Karen W. Gripp, Rikke S. Møller, Yaping Yang, (unknown), Elena Gardella	1
4	REEV: review, evaluate and explain variants 2024 ·Nucleic Acids Research ·(unknown), (unknown), (unknown), (unknown), Mikko Nieminen, R. Adam, Magdalena Danyel, (unknown), René Hägerling, Alexej Knaus, Stefan Mundlos, (unknown), Dominik Seelow, Nadja Ehmke, Martin A. Mensah, Felix Boschann, Dieter Beule, Manuel Holtgrewe	1
5	Primidone improves symptoms in TRPM3‐linked developmental and epileptic encephalopathy with spike‐and‐wave activation in sleep 2023 ·Epilepsia ·Lena‐Luise Becker, Denise Horn, Felix Boschann, (unknown), Thomas Voets, Joris Vriens, (unknown), Angela M. Kaindl	9
6	Novel noncanonical splice site variant causes mild CHD7‐related disorder with variable intrafamilial expressivity 2023 ·American Journal of Medical Genetics Part A ·Felix Boschann, (unknown), Marc Bloching, Johannes Grünhagen, (unknown), Denise Horn, (unknown)	1
7	Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy 2023 ·Frontiers in Neurology ·(unknown), Magdalena Danyel, Nina Erdmann, Felix Boschann, Cecilia Gunnarsson, Saskia Biskup, (unknown), (unknown), (unknown), Angela M. Kaindl	0
8	Hyper-IgE and Carcinoma in CADINS Disease 2022 ·Frontiers in Immunology ·(unknown), Julia Körholz, Felix Boschann, Mildred Sergon, Batsukh Dorjbal, (unknown), (unknown), (unknown), (unknown), (unknown), Martin W. Laaß, Reinhard Berner, (unknown), Joachim Roesler, Daniela E. Aust, Min Ae Lee‐Kirsch, Andrew L. Snow, Catharina Schuetz	11
9	Xq27.1 palindrome mediated interchromosomal insertion likely causes familial congenital bilateral laryngeal abductor paralysis (Plott syndrome) 2022 ·Journal of Human Genetics ·Felix Boschann, (unknown), Martin A. Mensah, (unknown), (unknown), Manuel Holtgrewe, Stefan Mundlos, Björn Fischer‐Zirnsak	3
10	Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders 2021 ·Clinical Genetics ·(unknown), (unknown), Bitten Schönewolf‐Greulich, Alexandra Afenjar, Magalie Barth, Felix Boschann, Diane Doummar, Tobias B. Haack, Boris Keren, Л. А. Лившиц, Davide Mei, Joohyun Park, Tiziana Pisano, (unknown), Muhammad Umair, Ahmed Waqas, Alban Ziegler, Renzo Guerrini, Rikke S. Møller, Zeynep Tümer	26
11	Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive 2021 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Nadja Ehmke, (unknown), (unknown), Barbara Plecko, Manuel Holtgrewe, Dominik Seelow, (unknown), Michael R. Speicher, Uwe Kornak, Denise Horn, Stefan Mundlos, Björn Fischer‐Zirnsak, Felix Boschann	12
12	Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly 2021 ·Genetics in Medicine ·Denise Horn, (unknown), (unknown), (unknown), Julián Nevado, (unknown), Nadja Ehmke, Pablo Lapunzina, Ghada A. Otaify, Samia A. Temtamy, Mona Aglan, Felix Boschann, Víctor L. Ruiz‐Pérez	5
13	Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis 2021 ·Journal of Neurology ·(unknown), Felix Boschann, Julia B. Hennermann, Gabriele Hahn, Andreas Hermann, Maja von der Hagen, Victoria Tüngler	4
14	An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndrome 2020 ·European Journal of Medical Genetics ·Felix Boschann, Björn Fischer‐Zirnsak, Thomas F. Wienker, Manuel Holtgrewe, Dominik Seelow, (unknown), (unknown), Raimund Fahsold, Denise Horn, Luitgard Graul‐Neumann	6
15	VarFish: comprehensive DNA variant analysis for diagnostics and research 2020 ·Nucleic Acids Research ·Manuel Holtgrewe, (unknown), Mikko Nieminen, Stefan Mundlos, Alexej Knaus, Uwe Kornak, Dominik Seelow, (unknown), Malte Spielmann, Björn Fischer‐Zirnsak, Felix Boschann, Ute I. Scholl, Nadja Ehmke, Dieter Beule	33
16	Differentiation of MISSLA and Fanconi anaemia by computer-aided image analysis and presentation of two novel MISSLA siblings 2019 ·European Journal of Human Genetics ·Magdalena Danyel, Zhuo Cheng, Christine Jung, Felix Boschann, Jean Tori Pantel, (unknown), Ricarda Flöttmann, (unknown), Ilja Demuth, Eamonn Sheridan, Stefan Mundlos, Denise Horn, Martin A. Mensah	6
17	Plasma Kynurenine Predicts Severity and Complications of Heart Failure and Associates with Established Biochemical and Clinical Markers of Disease 2019 ·Kidney & Blood Pressure Research ·Thomas Dschietzig, (unknown), (unknown), Felix Boschann, (unknown), (unknown), Franz Paul Armbruster, Dragić Banković, Andreas Meinitzer, Veselin Mitrović, Christoph Melzer	27
18	TGDS pathogenic variants cause Catel‐Manzke syndrome without hyperphalangy 2019 ·American Journal of Medical Genetics Part A ·Felix Boschann, Kyra E. Stuurman, Christiaan de Bruin, Marjon van Slegtenhorst, Hermine A. van Duyvenvoorde, Sarina G. Kant, Nadja Ehmke	4
19	Homoarginine Associates with Zonulin and Tryptophan - Findings in a High-Risk Cohort of Patients Carrying an AICD 2017 ·Clinical Laboratory ·(unknown), (unknown), Felix Boschann, (unknown), Franz Paul Armbruster, Andreas Meinitzer, Christoph Melzer, Thomas Dschietzig	1
20	Plasma Zonulin and its Association with Kidney Function, Severity of Heart Failure, and Metabolic Inflammation 2016 ·Clinical Laboratory ·Thomas Dschietzig, Felix Boschann, (unknown), Franz Paul Armbruster, Andreas Meinitzer, Dragić Banković, Veselin Mitrović, Christoph Melzer	13

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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