Vincent Strehlow

721 total citations
12 papers, 68 citations indexed

About

Vincent Strehlow is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Vincent Strehlow has authored 12 papers receiving a total of 68 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Vincent Strehlow's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Vincent Strehlow is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Vincent Strehlow collaborates with scholars based in Germany, Singapore and United States. Vincent Strehlow's co-authors include Jacqueline Leßig, Uta Reibetanz, Johannes R. Lemke, Steffen Syrbe, Thomas Dorn, Rhys H. Thomas, Nora Rapps, Mariëlle E.M. Swinkels, Scott J. Myers and Claudine Rieubland and has published in prestigious journals such as ACS Nano, Epilepsia and Human Mutation.

In The Last Decade

Vincent Strehlow

11 papers receiving 68 citations

Peers

Countries citing papers authored by Vincent Strehlow

Since Specialization

Citations

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

Fields of papers citing papers by Vincent Strehlow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Strehlow

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Strehlow. A scholar is included among the top collaborators of Vincent Strehlow 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 Vincent Strehlow. Vincent Strehlow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	KaRhab: an international online registry for cardiac rhabdomyomas 2025 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), Caroline G. Bergner, (unknown), (unknown), (unknown), (unknown), Steffen Syrbe, Robert Wágner, (unknown), N. S. Wolf, Michael Weidenbach, Vincent Strehlow	0
2	A Newborn with Cleft Palate Associated with PTEN Hamartoma Tumor Syndrome 2025 ·Clinics and Practice ·Ulf Nestler, Daniel Gräfe, Vincent Strehlow, (unknown), Andreas Merkenschlager, (unknown), (unknown)	1
3	Incorporating Nanopore Sequencing Into a Diverse Diagnostic Toolkit for Incontinentia Pigmenti 2025 ·Human Mutation ·(unknown), Denny Popp, Henry Oppermann, Vincent Strehlow, Maria Faßhauer, Bernt Popp, (unknown), (unknown)	1
4	Clinical Impact of Polygenic Risk Score for Breast Cancer Risk Prediction in 382 Individuals with Hereditary Breast and Ovarian Cancer Syndrome 2023 ·Cancers ·S. Stiller, Stephan Drukewitz, Kathleen Lehmann, Julia Hentschel, Vincent Strehlow	3
5	The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome 2022 ·Clinical Genetics ·Bernt Popp, Melanie Brügger, (unknown), Tobias Bartolomaeus, (unknown), Julia Hentschel, Nataliya Di Donato, Andreas Rump, Janina Gburek‐Augustat, Elisabeth Graf, Matias Wagner, Ina Sorge, Johannes R. Lemke, Thomas Meitinger, Rami Abou Jamra, Vincent Strehlow, Theresa Brunet	2
6	Compound‐heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy 2022 ·Epilepsia ·Vincent Strehlow, Claudine Rieubland, Sabina Gallati, Sukhan Kim, Scott J. Myers, Vincent Z. Peterson, Amy J. Ramsey, (unknown), Stephen F. Traynelis, Johannes R. Lemke	5
7	Full ablative versus fractional ablative laser therapy for Dowling–Degos disease 2018 ·Lasers in Surgery and Medicine ·(unknown), (unknown), Vincent Strehlow, (unknown), (unknown), Sonja Grunewald, Jan C. Simon, Manfred Kunz	5
8	Drug-Induced Loss of Preexcitation in Pediatric Patients with WPW Pattern During Electrophysiologic Study 2018 ·Pediatric Cardiology ·Christian Paech, (unknown), Vincent Strehlow, Roman Gebauer	5
9	Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome 2016 ·Molecular Syndromology ·Vincent Strehlow, Mariëlle E.M. Swinkels, Rhys H. Thomas, Nora Rapps, Steffen Syrbe, Thomas Dorn, Johannes R. Lemke	13
10	The spectrum of GRIN2A-associated disorders 2015 ·Max Planck Digital Library ·Vincent Strehlow, Henrike Heyne, Johannes R. Lemke	4
11	Development of LbL biopolymer capsules as a delivery system for the multilayer-assembled anti-inflammatory substance α1-antitrypsin 2013 ·Journal of Materials Chemistry B ·Vincent Strehlow, Jacqueline Leßig, (unknown), Uta Reibetanz	8
12	Inhibition of Human Neutrophil Elastase by α₁-Antitrypsin Functionalized Colloidal Microcarriers 2012 ·ACS Nano ·Uta Reibetanz, (unknown), (unknown), Vincent Strehlow, (unknown), Jacqueline Leßig	21

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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