Liesbeth Spruijt

4.4k citations

43 papers · 1.6k indexed · h-index 23

Co-authors: I.F.M. de Coo Arjen R. Mensenkamp Han G. Brunner Heleen H. Arts Ronald Roepman Dorus A. Mans Nicoline Hoogerbrugge Nine V.A.M. Knoers
Topics: Mitochondrial Function and Pathology (9 papers)Metabolism and Genetic Disorders (7 papers)BRCA gene mutations in cancer (6 papers)
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: Journal of Clinical Oncology Gastroenterology The Journal of Clinical Endocrinology & Metabolism
Partner nations: Netherlands United States Germany

In The Last Decade

Liesbeth Spruijt

42 papers receiving 1.6k citations

Peers

Countries citing papers authored by Liesbeth Spruijt

Since Specialization

Citations

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

Fields of papers citing papers by Liesbeth Spruijt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liesbeth Spruijt

This figure shows the co-authorship network connecting the top 25 collaborators of Liesbeth Spruijt. A scholar is included among the top collaborators of Liesbeth Spruijt 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 Liesbeth Spruijt. Liesbeth Spruijt 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	Evaluation of yield and experiences of age‐related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome 2020 ·International Journal of Cancer ·Janet R. Vos,(unknown),Liesbeth Spruijt,Riki W. Willems,(unknown),Arjen R. Mensenkamp,Edward M. Leter,Irıs D. Nagtegaal,Marjolijn J. L. Ligtenberg,Nicoline Hoogerbrugge,(unknown)	16
2	Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer 2015 ·Scientific Reports ·Richarda M. de Voer,(unknown),Arjen R. Mensenkamp,Alexander Hoischen,Christian Gilissen,(unknown),Liesbeth Spruijt,Wendy A. van Zelst-Stams,C. Marleen Kets,Eugène T.P. Verwiel,Irıs D. Nagtegaal,Hans K. Schackert,Ad Geurts van Kessel,Nicoline Hoogerbrugge,Marjolijn J. L. Ligtenberg,Roland P. Kuiper	56
3	More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling 2013 ·Familial Cancer ·(unknown),Wendy A.G. van Zelst–Stams,Liesbeth Spruijt,Arjen R. Mensenkamp,Marjolijn J. L. Ligtenberg,Han G. Brunner,Judith B. Prins,Nicoline Hoogerbrugge	35
4	Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes 2013 ·Familial Cancer ·(unknown),Judith B. Prins,Liesbeth Spruijt,C. Marleen Kets,Nicoline Hoogerbrugge	17
5	Added Value of Family History in Counseling About Risk of BRCA1/2 Mutation in Early-Onset Epithelial Ovarian Cancer 2013 ·International Journal of Gynecological Cancer ·M.A.D.W. de Jong,Catharina M. Mulders‐Manders,Nicoline Hoogerbrugge,Marjolijn J. L. Ligtenberg,Leon F.A.G. Massuger,Joanne A. de Hullu,Liesbeth Spruijt	3
6	Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome 2011 ·European Journal of Cancer ·Peggy Manders,Liesbeth Spruijt,C. Marleen Kets,H.W. Willems,Daniëlle Bodmer,Konnie M. Hebeda,Irıs D. Nagtegaal,J. Han van Krieken,Marjolijn J. L. Ligtenberg,Nicoline Hoogerbrugge	11
7	Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors 2011 ·Familial Cancer ·(unknown),Nils Rahner,Felix F. Brockschmidt,Verena Steinke,Philip Kahl,Tim Becker,Hans F. A. Vasen,Juul Wijnen,Carli Tops,Elke Holinski‐Feder,Marjolijn J. L. Ligtenberg,Liesbeth Spruijt,Heike Görgens,Susanne Stemmler,Matthias Kloor,Wolfgang Dietmaier,Johannes Schumacher,Markus M. Nöthen,Peter Propping	1
8	C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome 2011 ·Journal of Medical Genetics ·Heleen H. Arts,Ernie M.H.F. Bongers,Dorus A. Mans,Sylvia E. C. van Beersum,(unknown),Emine Bolat,Liesbeth Spruijt,Elisabeth A. M. Cornelissen,Janneke Schuurs-Hoeijmakers,Nicole de Leeuw,Valérie Cormier‐Daire,Han G. Brunner,Nine V.A.M. Knoers,Ronald Roepman	102
9	Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome 2010 ·The American Journal of Human Genetics ·Christian Gilissen,Heleen H. Arts,Alexander Hoischen,Liesbeth Spruijt,Dorus A. Mans,Peer Arts,Bart van Lier,Marloes Steehouwer,Jeroen van Reeuwijk,Sarina G. Kant,Ronald Roepman,Nine V.A.M. Knoers,Joris A. Veltman,Han G. Brunner	197
10	Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation 2009 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·(unknown),I.F.M. de Coo,Liesbeth Spruijt,L. Elly A. de Wit,Hubert J.M. Smeets,Wim J. Sluiter	19
11	A MELAS-Associated ND1 Mutation Causing Leber Hereditary Optic Neuropathy and Spastic Dystonia 2007 ·Archives of Neurology ·Liesbeth Spruijt,Hubert Smeets,Alexandra T.M. Hendrickx,(unknown),Anneke Maat‐Kievit,Kees Schoonderwoerd,Wim J. Sluiter,I.F.M. de Coo,Rogier Q. Hintzen	41
12	Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease 2007 ·Journal of Medical Genetics ·Marinus J. Blok,Liesbeth Spruijt,I.F.M. de Coo,Kees Schoonderwoerd,Alexandra T.M. Hendrickx,H.J.M. Smeets	49
13	Identification of a novel EYA1 mutation presenting in a newborn with laryngomalacia, glossoptosis, retrognathia, and pectus excavatum 2006 ·American Journal of Medical Genetics Part A ·Liesbeth Spruijt,Lies H. Hoefsloot,(unknown),Dick van Waardenburg,B. Kremer,Hein Brackel,Christine de Die‐Smulders	9
14	A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP) 2005 ·American Journal of Medical Genetics Part A ·Liesbeth Spruijt,Pieter Verdyck,Wim Van Hul,Wim Wuyts,Christine de Die‐Smulders	11
15	Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder 2005 ·The American Journal of Human Genetics ·Gavin Hudson,Sharon Keers,Patrick Yu Wai Man,Philip G. Griffiths,Kirsi Huoponen,Marja-Liisa Savontaus,Eeva Nikoskelainen,Massimo Zeviani,Franco Carrara,Rita Horváth,Veronika Karcagi,Liesbeth Spruijt,I.F.M. de Coo,Hubert J.M. Smeets,Patrick F. Chinnery	144
16	A 2‐bp deletion in the GJA1 gene is associated with oculo‐dento‐digital dysplasia with palmoplantar keratoderma 2004 ·American Journal of Medical Genetics Part A ·Maurice A. M. Van Steensel,Liesbeth Spruijt,I. van der Bürgt,Reno S. Bladergroen,Maarten H. Vermeer,Peter M. Steijlen,Michel van Geel	65
17	A patient with a de novo 15q24q26.1 interstitial deletion, developmental delay, mild dysmorphism, and very blue irises 2004 ·American Journal of Medical Genetics Part A ·Liesbeth Spruijt,J.J.M. Engelen,(unknown),(unknown),J. J. P. Schrander,C. T. R. M. Schrander‐Stumpel	7
18	Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic Neuropathy 2003 ·The American Journal of Human Genetics ·Neil Howell,Roelof‐Jan Oostra,P. A. Bolhuis,Liesbeth Spruijt,L. Clarke,David A. Mackey,(unknown),Corinna Herrnstadt	91
19	The Otolaryngological Manifestations of Mitochondrial Disease and the Risk of Neurodegeneration With Infection 2002 ·Archives of Otolaryngology - Head and Neck Surgery ·Joseph Edmonds,Daniel J. Kirse,Donald B. Kearns,Reena Deutsch,Liesbeth Spruijt,Robert K. Naviaux	61
20	Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetate 2001 ·Muscle & Nerve ·Liesbeth Spruijt,Robert K. Naviaux,(unknown),William L. Nyhan,Geoffrey Sheean,Richard Haas,Bruce A. Barshop	47

About Liesbeth Spruijt

Liesbeth Spruijt is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 43 papers that have together received 1.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (7 papers) and BRCA gene mutations in cancer (6 papers). The work is most often cited by research in Clinical Biochemistry (214 citations), Genetics (620 citations) and Molecular Biology (1.0k citations). Liesbeth Spruijt has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include I.F.M. de Coo, Arjen R. Mensenkamp, Han G. Brunner, Heleen H. Arts, Ronald Roepman, Dorus A. Mans, Nicoline Hoogerbrugge, Nine V.A.M. Knoers, Christian Gilissen and Christine de Die‐Smulders. Their work appears in journals such as Journal of Clinical Oncology, Gastroenterology and The Journal of Clinical Endocrinology & Metabolism.

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