Jane Hewitt

5.3k citations

74 papers · 4.2k indexed · 1 hit paper · h-index 33

Impact in

Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 2%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- RNA modifications and cancer
- Ubiquitin and proteasome pathways

Papers in

Structural Biology 2
Cell Biology 16

Co-authors: Prabhjit K. Grewal Rune R. Frants George W. Padberg Lorraine N. Clark Gert‐Jan B. van Ommen Tracy J. Wright Cisca Wijmenga Robert Williamson
Journals: Human Molecular Genetics (8 papers)Genomics (8 papers)Gene (7 papers)Mammalian Genome (4 papers)Neuromuscular Disorders (3 papers)
Partner nations: United Kingdom Netherlands United States

In The Last Decade

Jane Hewitt

74 papers receiving 4.1k citations

Hit Papers

align trajectories log scale

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy 1992 · 514 citations

Peers

Countries citing papers authored by Jane Hewitt

Since Specialization

Citations

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

Fields of papers citing papers by Jane Hewitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jane Hewitt, 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 Jane Hewitt Line = papers co-authored together Jane Hewitt links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients Neuromuscular Disorders ·Emma Humphrey, Deimantė Janulytė, Lam Le, Lucy Feng, Francesca Sciandra, A. Himoto, Jane Hewitt, Ian Holt, Andrea Brancaccio, Rita Barresi, Caroline A. Sewry, S. Brown, Glenn E. Morris	2014	5
2	Re-evaluation of the Role of Calcium Homeostasis Endoplasmic Reticulum Protein (CHERP) in Cellular Calcium Signaling Journal of Biological Chemistry ·Yaping Lin-Moshier, André Guarneri, LeeAnn Higgins, Natalie Sampson, Jane Hewitt, Jonathan S. Marchant	2012	76
3	Glycoproteomic characterization of recombinant mouse α-dystroglycan Glycobiology ·A. Y Smetanov, Paul G. Hitchen, Maria Panico, Howard R. Morris, David Mekhaiel, Richard J. Pleass, Anne Dell, Jane Hewitt, Stuart M. Haslam	2012	50
4	LARGE enzyme activity deciphered: a new therapeutic target for muscular dystrophies Genome Medicine ·Jane Hewitt	2012	3
5	Investigating the Functions of LARGE: Lessons from Mutant Mice Methods in enzymology on CD-ROM/Methods in enzymology ·Jane Hewitt	2010	2
6	Abnormal glycosylation of dystroglycan in human genetic disease Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jane Hewitt	2009	62
7	Genes required for functional glycosylation of dystroglycan are conserved in zebrafish☆☆Sequence data from this article have been deposited with the GenBank Data Library under Accession Nos. DQ826745 (Fukutin), DQ826746 (FKRP), DQ826747 (POMGnT1), DQ826748 (POMT1), and DQ826749 (POMT2). Genomics ·Christopher Moore, L. Stroosnijder, Jane Hewitt	2008	34
8	Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome Human Genetics ·Jeroen van Reeuwijk, Prabhjit K. Grewal, Mustafa A. Salih, Daniel Beltrán-Valero de Bernabé, Jenny M. McLaughlan, Caroline B. Michielse, Ralf Herrmann, Jane Hewitt, Alice Steinbrecher, Arpita Chokroborty, N. I. Ershov, Fabiana Coglianese, Han G. Brunner, Hans van Bokhoven, Thomas Voït	2007	101
9	A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophy Neuromuscular Disorders ·YASUHIRO SIMADA, Prabhjit K. Grewal, Christopher Moore, Jane Hewitt	2005	12
10	Glycosylation defects in inherited muscle disease Cellular and Molecular Life Sciences ·Jane Hewitt, Prabhjit K. Grewal	2003	24
11	De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10 The American Journal of Human Genetics ·Silvère M. van der Maarel, Giancarlo Deidda, Richard J.L.F. Lemmers, Petra G.M. van Overveld, Linda B. Labaume, Jane Hewitt, Lodewijk A. Sandkuijl, Egbert Bakker, Gert‐Jan B. van Ommen, George W. Padberg, Rune R. Frants	2000	116
12	Identification of a novel β-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35 Cytogenetic and Genome Research ·Michel van Geel, J.C.T. van Deutekom, В. С. Сидорчук, Richard J.L.F. Lemmers, Ш.М. Ахмедов, Jeffrey Boeckman, George W. Padberg, Jane Hewitt, Pieter J. de Jong, Rune R. Frants	2000	27
13	Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element Gene ·D. Vieira, M.-C. Beckers, Hao Ding, An S. De Vriese, Stéphane Plaisance, Silvère M. van der Maarel, George W. Padberg, Rune R. Frants, Jane Hewitt, Désiré Collen, Alexandra Belayew	1999	281
14	The murine urea transporter genes <i>Slc14a1</i> and <i>Slc14a2</i> occur in tandem on chromosome 18 Cytogenetic and Genome Research ·Robert A. Fenton, Jane Hewitt, Vincent Becaas, Fabio André Brand, Craig P. Smith	1999	32
15	High-resolution mapping of mouse Chromosome 8 identifies an evolutionary chromosomal breakpoint Mammalian Genome ·Prabhjit K. Grewal, Daniel J. Bolland, Ltl Tam, Jane Hewitt	1998	10
16	FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates Gene ·Prabhjit K. Grewal, Ltl Tam, Silvère M. van der Maarel, Rune R. Frants, Jane Hewitt	1998	34
17	Sensitivity of HincW to CpG methylation Nucleic Acids Research ·Laura N. Bull, Jane Hewitt, David R. Cox, R Myers	1993	4
18	Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11 Human Molecular Genetics ·Tracy J. Wright, Cisca Wijmenga, Lorraine N. Clark, Rune R. Frants, Robert Williamson, Jane Hewitt	1993	58
19	Structure and sequence of the human homeobox gene HOX7 Genomics ·Jane Hewitt, Lorraine N. Clark, Alasdair Ivens, S. Dahri	1991	60
20	The minor components of the rat asialoglycoprotein receptor are apically located in neonatal enterocytes Gastroenterology ·Ariana Milligan, Eun Y. Lee, Jane Hewitt, Jacques Baenziger, Seong Bin Pak, K DeSchryver-Kecskemeti, David Alpers	1991	15

About Jane Hewitt

Jane Hewitt is a scholar working on Structural Biology, Cell Biology, Molecular Biology, Cellular and Molecular Neuroscience and Genetics, having authored 74 papers that have together received 4.2k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (44 papers), RNA Research and Splicing (19 papers), Genetic Neurodegenerative Diseases (13 papers), Ubiquitin and proteasome pathways (10 papers), RNA modifications and cancer (9 papers), Neurogenetic and Muscular Disorders Research (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Pancreatic function and diabetes (5 papers). The work is most often cited by research in Genetics (722 citations), Molecular Biology (3.7k citations), Cellular and Molecular Neuroscience (676 citations), Cardiology and Cardiovascular Medicine (709 citations) and Cell Biology (383 citations). Jane Hewitt has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Prabhjit K. Grewal, Rune R. Frants, George W. Padberg, Lorraine N. Clark, Gert‐Jan B. van Ommen, Tracy J. Wright, Cisca Wijmenga, Robert Williamson, Marten H. Hofker and Robert Lyle. Their work appears in journals such as Human Molecular Genetics, Genomics, Gene, Mammalian Genome and Neuromuscular Disorders.

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