Sascha Vermeer

3.2k citations

39 papers · 1.2k indexed · h-index 17

Molecular Biology top 10%
Genetics top 5%
Cellular and Molecular Neuroscience top 5%
Neurology top 5%
Genetics top 10%

Co-authors: Bart P.C. van de Warrenburg Hans Scheffer Rowdy Meijer Michèl A.A.P. Willemsen Susanne T. de Bot H.P.H. Kremer Barbara Karczeski Pasi A. Koivisto
Topics: Genetic Neurodegenerative Diseases (20 papers)Mitochondrial Function and Pathology (13 papers)Neurological diseases and metabolism (5 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Genetics
Journals: The Journal of Clinical Endocrinology & Metabolism Neurology CHEST Journal
Partner nations: Netherlands Belgium United Kingdom

In The Last Decade

Sascha Vermeer

37 papers receiving 1.2k citations

Peers

Countries citing papers authored by Sascha Vermeer

Since Specialization

Citations

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

Fields of papers citing papers by Sascha Vermeer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sascha Vermeer

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Hypogonadotropic Hypogonadism as First Presentation of the Severe Neuroendocrine Disorder Caused by RNF216 2024 ·JCEM Case Reports ·Anne Rochtus,(unknown),(unknown),Sascha Vermeer,Leen Antonio	1
2	PHARC syndrome: an overview 2024 ·Orphanet Journal of Rare Diseases ·(unknown),Patrick Callaerts,Sascha Vermeer	3
3	Intrafamilial Correlation and Variability in the Clinical Evolution of Pulmonary Fibrosis 2023 ·CHEST Journal ·(unknown),Adriana Dubbeldam,(unknown),(unknown),Laurens De Sadeleer,(unknown),Ellen De Langhe,Jonas Yserbyt,Birgit Weynand,Marianne Carlon,Johny Verschakelen,Sascha Vermeer,Stijn E. Verleden,Wim Wuyts	1
4	The MUC5B Promoter Polymorphism is Not Associated With Non-ILD Chronic Respiratory Diseases or Post-transplant Outcome 2022 ·Transplant International ·(unknown),Stijn E. Verleden,Laurens De Sadeleer,Anke Van Herck,Annelore Sacreas,Arno Vanstapel,Janne Kaes,(unknown),(unknown),David Ruttens,Diether Lambrechts,Sascha Vermeer,Laurens J. Ceulemans,Dirk Van Raemdonck,Laurent Godinas,Jonas Yserbyt,Bart Vanaudenaerde,Geert M. Verleden,Robin Vos,Wim Wuyts	0
5	Case Report: An Unusual Course of Angiosarcoma After Lung Transplantation 2022 ·Frontiers in Immunology ·Saskia Bos,Liesbeth Daniëls,Lucienne Michaux,Isabelle Vanden Bempt,Sascha Vermeer,Feng Jung Sherida H. Woei-A-Jin,Patrick Schöffski,Birgit Weynand,Raf Sciot,Sabine Declercq,Laurens J. Ceulemans,Laurent Godinas,Geert M. Verleden,Dirk Van Raemdonck,Lieven Dupont,Robin Vos,(unknown)	1
6	RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement 2021 ·European Journal of Neurology ·(unknown),Matthieu Moisse,Valérie Race,(unknown),Liesbeth Keldermans,Sascha Vermeer,Hilde Van Esch,Kristl G. Claeys,Philip Van Damme	6
7	Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders 2016 ·European Journal of Human Genetics ·Bart P.C. van de Warrenburg,Meyke Schouten,Susanne T. de Bot,Sascha Vermeer,Rowdy Meijer,Maartje Pennings,Christian Gilissen,(unknown),Hans Scheffer,Erik‐Jan Kamsteeg	76
8	A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay 2016 ·Human Molecular Genetics ·Teisha Y. Bradshaw,Lisa E. L. Romano,(unknown),Suran Nethisinghe,Rosella Abeti,Gregory J. Michael,Paola Giunti,Sascha Vermeer,J. Paul Chapple	45
9	Marinesco-Sjögren syndrome due to SIL1 mutations with a comment on the clinical phenotype 2012 ·European Journal of Paediatric Neurology ·(unknown),Anna‐Kaisa Anttonen,Anna‐Elina Lehesjoki,Éva Morava,Saskia B. Wortmann,Sascha Vermeer,Bart P.C. van de Warrenburg,Michèl A.A.P. Willemsen	16
10	Cerebellar Cognitive Affective Syndrome and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: A Report of Two Male Sibs 2012 ·Psychopathology ·W.M.A. Verhoeven,J.I.M. Egger,(unknown),Berry Kremer,Sascha Vermeer,Bart P.C. van de Warrenburg	15
11	Neonatal onset autosomal dominant polycystic kidney disease (ADPKD) in a patient homozygous for a PKD2 missense mutation due to uniparental disomy 2011 ·Journal of Medical Genetics ·Monique Losekoot,Claudia Ruivenkamp,(unknown),(unknown),Linda Vijfhuizen,Sascha Vermeer,Henry Dijkman,Elisabeth A. M. Cornelissen,Ernie M.H.F. Bongers,Dorien J.M. Peters	30
12	Autosomal recessive cerebellar ataxias: the current state of affairs 2011 ·Journal of Medical Genetics ·Sascha Vermeer,Bart P.C. van de Warrenburg,Michèl A.A.P. Willemsen,(unknown),Hans Scheffer,B Kremer,Nine Knoers	31
13	Massively parallel sequencing of ataxia genes after array-based enrichment 2010 ·Human Mutation ·Alexander Hoischen,Christian Gilissen,Peer Arts,Nienke Wieskamp,Walter van der Vliet,Sascha Vermeer,Marloes Steehouwer,Petra de Vries,Rowdy Meijer,(unknown),Nine V.A.M. Knoers,Michael F. Buckley,Hans Scheffer,Joris A. Veltman	63
14	Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region 2010 ·Epilepsia ·(unknown),Ingo Helbig,(unknown),(unknown),Holger Tönnies,Hiltrud Muhle,(unknown),Sascha Vermeer,Rolph Pfundt,Jürgen Sperner,Irina Stefanova,Gabriele Gillessen‐Kaesbach,Sarah von Spiczak,Andreas van Baalen,Rainer Boor,Reiner Siebert,Ulrich Stephani,Almuth Caliebe	65
15	Autosomal Recessive Mental Retardation, Deafness, Ankylosis, and Mild Hypophosphatemia Associated with a NovelANKHMutation in a Consanguineous Family 2010 ·The Journal of Clinical Endocrinology & Metabolism ·Éva Morava,Jirko Kühnisch,Jefte M. Drijvers,Joris H. Robben,Cor W. R. J. Cremers,(unknown),A. J. W. Branten,Sabine Stumpp,(unknown),Krysta Voesenek,Sascha Vermeer,Angelien Heister,Hedi L. Claahsen‐van der Grinten,(unknown),Michèl A.A.P. Willemsen,Dirk J. Lefeber,Peter M.T. Deen,Uwe Kornak,Hannie Kremer,Ron A. Wevers	31
16	GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype 2009 ·Human Mutation ·William A. Paznekas,Barbara Karczeski,Sascha Vermeer,R. Brian Lowry,Martin B. Delatycki,(unknown),Pasi A. Koivisto,Lionel Van Maldergem,Simeon A. Boyadjiev,Joann Bodurtha,Ethylin Wang Jabs	208
17	ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia 2008 ·Neurogenetics ·Sascha Vermeer,Rowdy Meijer,(unknown),Janneke Timmermans,J.R.M. Cruysberg,(unknown),Helenius J. Schelhaas,Bart P.C. van de Warrenburg,Nine Knoers,Hans Scheffer,B. Kremer	105
18	Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients 2008 ·The American Journal of Human Genetics ·Julie Vogt,Benjamin J. Harrison,Hayley Spearman,Judy Cossins,Sascha Vermeer,(unknown),Neil V. Morgan,David Beeson,Eamonn R. Maher	75
19	Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature 2008 ·Human Mutation ·Bert Callewaert,Bart Loeys,Anna Ficcadenti,Sascha Vermeer,Magnus Landgren,Hester Y. Kroes,Yuval Yaron,Michael Pope,Nicola Foulds,Odile Boute,Francisco Galán,Helen Kingston,Nathalie Van der Aa,(unknown),Mariëlle E.M. Swinkels,Carina Wallgren‐Pettersson,Orazio Gabrielli,Julie De Backer,Paul Coucke,Anne M. De Paepe	62
20	Novel mutations in three patients with LGMD2C with phenotypic differences 2004 ·Pediatric Neurology ·Sascha Vermeer,Aad Verrips,Michèl A.A.P. Willemsen,H. J. ter Laak,Ieke B. Ginjaar,Ben C.J. Hamel	10

About Sascha Vermeer

Sascha Vermeer is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology, having authored 39 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (20 papers), Mitochondrial Function and Pathology (13 papers) and Neurological diseases and metabolism (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (383 citations), Neurology (162 citations) and Genetics (467 citations). Sascha Vermeer has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Bart P.C. van de Warrenburg, Hans Scheffer, Rowdy Meijer, Michèl A.A.P. Willemsen, Susanne T. de Bot, H.P.H. Kremer, Barbara Karczeski, Pasi A. Koivisto, Ethylin Wang Jabs and Martin B. Delatycki. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and CHEST Journal.

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.

Explore authors with similar magnitude of impact