Jasper J. Saris

4.7k citations

34 papers · 3.3k indexed · 2 hit papers · h-index 19

Molecular Biology top 5%
Genetics top 0.5%
Cardiology and Cardiovascular Medicine top 5%
Endocrinology, Diabetes and Metabolism top 5%
Pathology and Forensic Medicine top 5%

Co-authors: Dorien J.M. Peters Martijn H. Breuning Alkis Pierides Constantinos Deltas Raoul C. M. Hennekam Niels Tommerup Hans G. Dauwerse A.H. Jan Danser
Topics: Genetic Syndromes and Imprinting (12 papers)Genetic and Kidney Cyst Diseases (12 papers)Renal and related cancers (10 papers)
Cited by: Developmental Biology Genetics Molecular Biology
Journals: Nature Science The Lancet
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Jasper J. Saris

34 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein

1996 1.1k citations Toshio Mochizuki, Tomohito Hayashi et al. profile →
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1995 904 citations Rachel H. Giles, Hans G. Dauwerse et al. Nature profile →

Peers

Countries citing papers authored by Jasper J. Saris

Since Specialization

Citations

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

Fields of papers citing papers by Jasper J. Saris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jasper J. Saris. 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 Jasper J. Saris. The network helps show where Jasper J. Saris may publish in the future.

Co-authorship network of co-authors of Jasper J. Saris

This figure shows the co-authorship network connecting the top 25 collaborators of Jasper J. Saris. A scholar is included among the top collaborators of Jasper J. Saris 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 Jasper J. Saris. Jasper J. Saris 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	Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome 2023 ·Human Mutation ·Hannie Douben,Marianne Hoogeveen‐Westerveld,Mark Nellist,(unknown),(unknown),(unknown),(unknown),Leontine van Unen,Peter Elfferich,(unknown),Yolande van Bever,Margreethe van Vliet,Rianne Oostenbrink,Jasper J. Saris,Anja Wagner,Yvette van Ierland,Tjakko J. van Ham,Rick van Minkelen	2
2	Neurovascular abnormalities in patients with Loeys-Dietz syndrome type III 2022 ·European Journal of Medical Genetics ·(unknown),(unknown),(unknown),(unknown),Jasper J. Saris,Adriaan C.G.M. van Es,Pieter‐Jan van Doormaal,(unknown),Fop van Kooten,Jolien W. Roos‐Hesselink	2
3	Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis 2020 ·Molecular Therapy — Methods & Clinical Development ·Stijn L.M. in ‘t Groen,(unknown),(unknown),Johanna M. P. van den Hout,Hannie Douben,Trijnie Dijkhuizen,David Cassiman,Peter Witters,(unknown),Annelies de Klein,(unknown),Jasper J. Saris,Lies H. Hoefsloot,Ans T. van der Ploeg,Atze J. Bergsma,W.W.M. Pim Pijnappel	13
4	Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays 2019 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),Marianne Hoogeveen‐Westerveld,Marian A. Kroos,Sirpa Ala‐Mello,Olga Amaral,Clara Sá-Miranda,Irene Mavridou,Helen Michelakakis,K Naess,Frans W. Verheijen,Lies H. Hoefsloot,Trijnie Dijkhuizen,(unknown),(unknown),Ans T. van der Ploeg,W.W.M. Pim Pijnappel,Jasper J. Saris,Dicky Halley	8
5	N-Acetylglutamate Synthase Deficiency Due to a Recurrent Sequence Variant in the N-acetylglutamate Synthase Enhancer Region 2018 ·Scientific Reports ·Monique Williams,Alberto Burlina,Laura Rubert,Giulia Polo,George J. G. Ruijter,Myrthe van den Born,Véronique Rüfenacht,(unknown),Laura J. C. M. van Zutven,Mendel Tuchman,Jasper J. Saris,Johannes Häberle,Ljubica Caldovic	8
6	Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis 2018 ·European Journal of Medical Genetics ·(unknown),Rachel Schot,A. Jeannette M. Hoogeboom,Carsten R. Lincke,I.F.M. de Coo,Maarten H. Lequin,Marjolein H. G. Dremmen,Leontine van Unen,Jasper J. Saris,Anna Jansen,Marjon A. van Slegtenhorst,Martina Wilke,Grazia M.S. Mancini	7
7	Neonatal screening for profound biotinidase deficiency in the Netherlands: consequences and considerations 2016 ·European Journal of Human Genetics ·(unknown),Michelle E. Kruijshaar,Rick van Minkelen,W. Onkenhout,Frans W. Verheijen,(unknown),Francjan J. van Spronsen,Ans T. van der Ploeg,Klary E. Niezen‐Koning,Jasper J. Saris,Monique Williams	18
8	Complete FXN Deletion in a Patient with Friedreich's Ataxia 2012 ·Genetic Testing and Molecular Biomarkers ·Ans M.W. van den Ouweland,Rick van Minkelen,(unknown),Carine Wouters,(unknown),Wout H. Deelen,(unknown),(unknown),Jasper J. Saris,Dicky Halley	7
9	Prorenin Induces Intracellular Signaling in Cardiomyocytes Independently of Angiotensin II 2006 ·Hypertension ·Jasper J. Saris,Peter A.C. ’t Hoen,Ingrid M. Garrelds,Dick H. W. Dekkers,Johan T. den Dunnen,Jos M. J. Lamers,A.H. Jan Danser	196
10	Prorenin Uptake in the Heart: a Prerequisite for Local Angiotensin Generation? 2002 ·Journal of Molecular and Cellular Cardiology ·A.H. Jan Danser,Jasper J. Saris	23
11	Cellular localization and tissue distribution of polycystin-1 1999 ·The Journal of Pathology ·Dorien J.M. Peters,(unknown),Lia Spruit,Jasper J. Saris,Martijn H. Breuning,Jan A. Bruijn,Emile de Heer	69
12	A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2) 1997 ·The American Journal of Human Genetics ·Barbera Veldhuisen,Jasper J. Saris,Simone de Haij,Tomohito Hayashi,David M. Reynolds,Toshio Mochizuki,R Elles,Ragnheiður Fossdal,Nadja Bogdanova,Marjan A. van Dijk,Eliécer Coto,David Ravine,Søren Nørby,C. Verellen‐Dumoulin,M.H. Breuning,Stefan Somlo,Dorien J.M. Peters	77
13	Mutation Detection in the Repeated Part of the PKD1 Gene 1997 ·The American Journal of Human Genetics ·Jeroen Roelfsema,Lia Spruit,Jasper J. Saris,Peter C. Chang,Yves Pirson,Gert‐Jan B. van Ommen,Dorien J.M. Peters,Martijn H. Breuning	35
14	Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBPbreakdown → 1995 ·Nature ·(unknown),Rachel H. Giles,Hans G. Dauwerse,Jasper J. Saris,Raoul C. M. Hennekam,Mitsuo Masuno,Niels Tommerup,Gert‐Jan B. van Ommen,Richard H. Goodman,Dorien J.M. Peters,Martijn H. Breuning	904
15	A CA repeat polymorphism at D11S1383 1994 ·Human Molecular Genetics ·Jasper J. Saris,Rolf H. A. M. Vossen,Egbert Bakker	1
16	Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease 1993 ·Nature Genetics ·Dorien J.M. Peters,Lia Spruit,Jasper J. Saris,David Ravine,Lodewijk A. Sandkuijl,Ragnheiður Fossdal,(unknown),Ronald van Eijk,Søren Nørby,Constantinos Deltas,Alkis Pierides,(unknown),(unknown),G.J.B. van Ommen,M.H. Breuning	192
17	Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers 1992 ·Genomics ·Stefan Somlo,Brunhilde Wirth,Gregory G. Germino,Debra Weinstat‐Saslow,Gerald A.J. Gillespie,Heinz Himmelbauer,(unknown),Paul Coucke,Patrick J. Willems,Lucien Bachner,Eliécer Coto,Carlos López‐Larrea,Belén Peral,(unknown),Jasper J. Saris,Martijn H. Breuning,Anna‐Maria Frischauf,Stephen T. Reeders	29
18	Evaluation of a cosmid contig physical map of human chromosome 16 1992 ·Genomics ·Raymond L. Stallings,Norman A. Doggett,David F. Callen,Sinoula Apostolou,(unknown),J.K. Nancarrow,S.A. Whitmore,Peter C. Harris,(unknown),Martijn H. Breuning,Jasper J. Saris,James W. Fickett,(unknown),David C. Torney,C.E. Hildebrand,Robert K. Moyzis	36
19	Probe 218EP6 (D16S246) detects RFLP's close to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 1990 ·Nucleic Acids Research ·F.G.M. Snijdewint,Jasper J. Saris,Johannes G. Dauwerse,M.H. Breuning,G.J.B. van Ommen	11
20	IMPROVED EARLY DIAGNOSIS OF ADULT POLYCYSTIC KIDNEY DISEASE WITH FLANKING DNA MARKERS 1987 ·The Lancet ·M.H. Breuning,HG Brunner,Jasper J. Saris,G.J.B. van Ommen,Stephen T. Reeders,Jacob W. IJdo,(unknown),P. Pearson	64

About Jasper J. Saris

Jasper J. Saris is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 34 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (12 papers), Genetic and Kidney Cyst Diseases (12 papers) and Renal and related cancers (10 papers). The work is most often cited by research in Developmental Biology (227 citations), Genetics (2.0k citations) and Molecular Biology (2.2k citations). Jasper J. Saris has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Dorien J.M. Peters, Martijn H. Breuning, Alkis Pierides, Constantinos Deltas, Raoul C. M. Hennekam, Niels Tommerup, Hans G. Dauwerse, A.H. Jan Danser, Gert‐Jan B. van Ommen and Richard H. Goodman. Their work appears in journals such as Nature, Science and The Lancet.

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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