Mark Nellist

10.3k citations

72 papers · 3.3k indexed · h-index 31

Impact in

Physiology top 1%
- Tuberous Sclerosis Complex Research
- Histiocytic Disorders and Treatments
Oncology top 5%
- Polyomavirus and related diseases

Papers in ⓘ

Physiology 57
- Tuberous Sclerosis Complex Research 57
- Histiocytic Disorders and Treatments 20
Oncology 23
- Polyomavirus and related diseases 21

Co-authors: Dicky Halley (28 shared papers)Miriam Goedbloed (11 shared papers)Ans van den Ouweland (15 shared papers)Floor E. Jansen (10 shared papers)Marianne Hoogeveen‐Westerveld (20 shared papers)Ans M.W. van den Ouweland (6 shared papers)Bernard A. Zonnenberg (4 shared papers)Eleonora Aronica (6 shared papers)
Journals: Human Mutation (9 papers)European Journal of Human Genetics (7 papers)Journal of Medical Genetics (4 papers)Neurology (3 papers)Journal of Biological Chemistry (3 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Mark Nellist

70 papers receiving 3.3k citations

Peers

Countries citing papers authored by Mark Nellist

Since Specialization

Citations

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

Fields of papers citing papers by Mark Nellist

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mark Nellist, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mark Nellist Line = papers co-authored together Mark Nellist links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease — a contiguous gene syndrome Nature Genetics ·Phillip T. Brook-Carter, Belén Peral, Christopher J. Ward, Peter Thompson, Jim R. Hughes, Magitha M. Maheshwar, Mark Nellist, Vicki Gamble, Peter C. Harris, Julian R. Sampson	1994	355
2	Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex European Journal of Human Genetics ·Őzgür Sancak, Mark Nellist, Miriam Goedbloed, Peter Elfferich, Carine Wouters, Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Dicky Halley, Ans van den Ouweland	2005	344
3	Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma Modern Pathology ·Anna E. Koopmans, Robert M. Verdijk, Rutger W. W. Brouwer, Thierry van den Bosch, Mike M P van den Berg, Jolanda Vaarwater, Christel Kockx, Dion Paridaens, Nicole C. Naus, Mark Nellist, Wilfred F. J. van IJcken, Emine Kılıç, Annelies de Klein	2014	168
4	Cognitive impairment in tuberous sclerosis complex is a multifactorial condition Neurology ·Floor E. Jansen, Koen L. Vincken, Ale Algra, Petronella Anbeek, Olga Braams, Mark Nellist, Bernard A. Zonnenberg, A. Jennekens‐Schinkel, Ans van den Ouweland, Dicky Halley, Alexander C. van Huffelen, Onno van Nieuwenhuizen	2007	155
5	Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex Epilepsy Research ·Karin Boer, Floor E. Jansen, Mark Nellist, Sandra Redeker, A.M.W. van den Ouweland, Wim G.M. Spliet, Onno van Nieuwenhuizen, Dirk Troost, Peter B. Crino, Eleonora Aronica	2007	155
6	Characterization of the Cytosolic Tuberin-Hamartin Complex Journal of Biological Chemistry ·Mark Nellist, Marjon A. van Slegtenhorst, Miriam Goedbloed, Ans M.W. van den Ouweland, Dicky Halley, Peter van der Sluijs	1999	148
7	Gene Expression Analysis of Tuberous Sclerosis Complex Cortical Tubers Reveals Increased Expression of Adhesion and Inflammatory Factors Brain Pathology ·Karin Boer, Peter B. Crino, Jan A. Gorter, Mark Nellist, Floor E. Jansen, Wim G.M. Spliet, Peter C. van Rijen, Floyd Wittink, Timo M. Breit, Dirk Troost, Wytse J. Wadman, Eleonora Aronica	2009	113
8	Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation Journal of Medical Genetics ·Marjon van Slegtenhorst, Senno Verhoef, A.M.P. Tempelaars, Lida Bakker, Qi Wang, Marja W. Wessels, Remco Bakker, Mark Nellist, Dick Lindhout, Dicky Halley, Ans van den Ouweland	1999	105
9	Fetal Brain Lesions in Tuberous Sclerosis Complex: TORC1 Activation and Inflammation Brain Pathology ·Avanita S. Prabowo, Jasper J. Anink, Martin Lammens, Mark Nellist, Ans M.W. van den Ouweland, Homa Adle‐Biassette, Harvey B. Sarnat, Laura Flores‐Sarnat, Peter B. Crino, Eleonora Aronica	2012	97
10	Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex Neuropathology ·Karin Boer, Dirk Troost, Floor E. Jansen, Mark Nellist, Ans M.W. van den Ouweland, Jeroen J.G. Geurts, Wim G.M. Spliet, Peter B. Crino, Eleonora Aronica	2008	91
11	Overlapping neurologic and cognitive phenotypes in patients with TSC1 or TSC2 mutations Neurology ·Floor E. Jansen, Olga Braams, Koen L. Vincken, Ale Algra, Petronella Anbeek, A. Jennekens‐Schinkel, Dicky Halley, Bernard A. Zonnenberg, Ans van den Ouweland, Alexander C. van Huffelen, Onno van Nieuwenhuizen, Mark Nellist	2007	73
12	Distinct effects of single amino-acid changes to tuberin on the function of the tuberin–hamartin complex European Journal of Human Genetics ·Mark Nellist, Őzgür Sancak, Miriam Goedbloed, Christan F. Rohé, Diana van Netten, Karin Mayer, Aimee Tucker-Williams, Ans M.W. van den Ouweland, Dicky Halley	2004	65
13	TORC1‐dependent epilepsy caused by acute biallelic Tsc1 deletion in adult mice Annals of Neurology ·Elisabeth Abs, Susanna M. I. Goorden, Jadwiga Schreiber, Iris E. Overwater, Marianne Hoogeveen‐Westerveld, Caroline F. Bruinsma, Elvedin Aganović, Nils Z. Borgesius, Mark Nellist, Ype Elgersma	2013	65
14	Identification and Characterization of the Interaction between Tuberin and 14-3-3ζ Journal of Biological Chemistry ·Mark Nellist, Miriam Goedbloed, Christa de Winter, Brenda Verhaaf, Anita Jankie, Arnold Reuser, Ans M.W. van den Ouweland, Peter van der Sluijs, Dicky Halley	2002	64
15	Rheb Is Essential for Murine Development Molecular and Cellular Biology ·Susanna M. I. Goorden, Marianne Hoogeveen‐Westerveld, Caroline Cheng, Geeske M. van Woerden, Melika Mozaffari, Laura Post, Henricus J. Duckers, Mark Nellist, Ype Elgersma	2011	62
16	Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations BMC Medical Genetics ·Mark Nellist, Rutger W. W. Brouwer, Christel Kockx, Monique van Veghel‐Plandsoen, Caroline Withagen-Hermans, Lida Prins-Bakker, Marianne Hoogeveen‐Westerveld, Alan Mršić, Mike MP van den Berg, Anna E. Koopmans, Marie‐Claire Y. de Wit, Floor E. Jansen, Anneke Maat‐Kievit, Ans van den Ouweland, Dicky Halley, Annelies de Klein, Wilfred F. J. van IJcken	2015	58
17	Comparative Analysis and Genomic Structure of the Tuberous Sclerosis 2 (TSC2) Gene in Human and Pufferfish Human Molecular Genetics ·Magitha M. Maheshwar, Richard Sandford, Mark Nellist, Jeremy P. Cheadle, Barbara Sgotto, Mark D. Vaudin, Julian R. Sampson	1996	56
18	Alternative Splicing of the Tuberous Sclerosis 2 (TSC2) Gene in Human and Mouse Tissues Genomics ·Lin Xu, Christopher J. Sterner, Magitha M. Maheshwar, Peter J. Wilson, Mark Nellist, Priscilla Short, Jonathan L. Haines, Julian R. Sampson, Vijaya Ramesh	1995	53
19	Functional Assessment ofTSC2 Variants Identified in Individuals with Tuberous Sclerosis Complex Human Mutation ·Marianne Hoogeveen‐Westerveld, Rosemary Ekong, (unknown), Karin Mayer, N. Lannoy, Frances Elmslie, (unknown), Kira A. Dies, Carl Thompson, Steven Sparagana, Peter Davies, Agnies M. van Eeghen, Dicky Halley, Mark Nellist	2012	53
20	Cellular localization of metabotropic glutamate receptors in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex Neuroscience ·Karin Boer, Dirk Troost, Wendy Timmermans, Jan A. Gorter, Wim G.M. Spliet, Mark Nellist, Floor E. Jansen, Eleonora Aronica	2008	46

About Mark Nellist

Mark Nellist is a scholar working on Physiology, Oncology, Pathology and Forensic Medicine, Genetics and Molecular Biology, having authored 72 papers that have together received 3.3k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (57 papers), Polyomavirus and related diseases (21 papers), Histiocytic Disorders and Treatments (20 papers), PI3K/AKT/mTOR signaling in cancer (10 papers), Genetic and Kidney Cyst Diseases (9 papers), Tumors and Oncological Cases (9 papers), Kruppel-like factors research (5 papers) and Neurofibromatosis and Schwannoma Cases (5 papers). The work is most often cited by research in Physiology (2.1k citations), Oncology (871 citations), Genetics (770 citations), Molecular Biology (1.4k citations) and Pathology and Forensic Medicine (299 citations). Mark Nellist has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Dicky Halley, Miriam Goedbloed, Ans van den Ouweland, Floor E. Jansen, Marianne Hoogeveen‐Westerveld, Ans M.W. van den Ouweland, Bernard A. Zonnenberg, Eleonora Aronica, Magitha M. Maheshwar and Senno Verhoef. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Journal of Medical Genetics, Neurology and Journal of Biological Chemistry.

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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