Isabelle Nelson

2.8k citations

49 papers · 1.5k · h-index 23

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Molecular Biology top 10%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- Muscle Physiology and Disorders
- RNA modifications and cancer
- RNA Research and Splicing

Papers in

Molecular Biology 41
- Mitochondrial Function and Pathology 26
- ATP Synthase and ATPases Research 11
- RNA Research and Splicing 8
- Muscle Physiology and Disorders 6
- RNA modifications and cancer 5
Clinical Biochemistry 20
- Metabolism and Genetic Disorders 20

Co-authors: Michael G. Hanna (11 shared papers)J A Morgan-Hughes (7 shared papers)Nicholas Wood (4 shared papers)A E Harding (4 shared papers)Patrick Lestienne (10 shared papers)Jonathan M. Cooper (3 shared papers)Norma B. Romero (11 shared papers)Shamima Rahman (3 shared papers)
Journals: Neuromuscular Disorders (9 papers)Neurology (5 papers)Journal of Neuromuscular Diseases (3 papers)Journal of the Neurological Sciences (3 papers)Biochemical and Biophysical Research Communications (2 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Isabelle Nelson

48 papers receiving 1.4k citations

Peers

Countries citing papers authored by Isabelle Nelson

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Nelson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Isabelle Nelson, 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 Isabelle Nelson Line = papers co-authored together Isabelle Nelson 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 49 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Missense Mutation of Cytochrome Oxidase Subunit II Causes Defective Assembly and Myopathy The American Journal of Human Genetics ·Shamima Rahman, Jan‐Willem Taanman, Jonathan M. Cooper, Isabelle Nelson, I. Hargreaves, Brigitte Meunier, Michael G. Hanna, (unknown), Roderick Capaldi, Brian Lake, James V. Leonard, Anthony H.V. Schapira	1999	113
2	Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA The American Journal of Human Genetics ·Michael G. Hanna, Isabelle Nelson, Shamima Rahman, R. Lane, J. Land, S Heales, Jonathan M. Cooper, Anthony H.V. Schapira, J A Morgan-Hughes, Nicholas Wood	1998	111
3	The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS Annals of Neurology ·Teeratorn Pulkes, L. H. Eunson, Victor Patterson, Asra Tus Saleha Siddiqui, Nicholas Wood, Isabelle Nelson, J A Morgan-Hughes, Michael G. Hanna	1999	96
4	Distinctive Serum miRNA Profile in Mouse Models of Striated Muscular Pathologies PLoS ONE ·Nicolas Vignier, Fatima Amor, Paul Fogel, Angélique Duvallet, Jérôme Poupiot, Sabine Charrier, Michel Arock, Marie Montus, Isabelle Nelson, (unknown), Lucie Carrier, Laurent Servais, Thomas Voit, Gisèle Bonne, David Israeli	2013	89
5	SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years Neurology ·Michito Namekawa, Pascale Ribaı̈, Isabelle Nelson, Sylvie Forlani, Florence Fellmann, Cyril Goizet, Christel Depienne, Giovanni Stévanin, Merle Ruberg, Alexandra Dürr, Alexis Brice	2006	81
6	MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity Journal of Neurology Neurosurgery & Psychiatry ·Michael G. Hanna, Isabelle Nelson, J A Morgan-Hughes, Nicholas Wood	1998	70
7	Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies Nucleic Acids Research ·Françoise Degoul, Isabelle Nelson, Serge Amselem, Norma B. Romero, B. Obermaier–Kusser, G Ponsot, C. Marsac, Patrick Lestienne	1991	64
8	Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation. PubMed ·Michael G. Hanna, Isabelle Nelson, M G Sweeney, Jonathan M. Cooper, Peter Watkins, J A Morgan-Hughes, A E Harding	1995	64
9	Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome Nucleic Acids Research ·Isabelle Nelson, Françoise Degoul, B. Obermaier–Kusser, Norma B. Romero, C Borrone, C. Marsac, Jean‐Luc Vayssière, Klaus-Dieter Gerbitz, Michel Fardeau, G Ponsot, Patrick Lestienne	1989	56
10	A mitochondrial DNA tRNA ^Val point mutation associated with adult-onset Leigh syndrome Neurology ·R. M. Chalmers, Phillipa J. Lamont, Isabelle Nelson, David W. Ellison, Neil H. Thomas, A E Harding, Simon Hammans	1997	56
11	A new mitochondrial DNA mutation associated with progressive dementia and chorea: A clinical, pathological, and molecular genetic study Annals of Neurology ·Isabelle Nelson, Michael G. Hanna, N. Alsanjari, F Scaravilli, J A Morgan-Hughes, A. E. Harding	1995	55
12	Depletion of mitochondrial DNA by ddC in untransformed human cell lines Somatic Cell and Molecular Genetics ·Isabelle Nelson, Michael G. Hanna, Nicholas Wood, A E Harding	1997	39
13	Higher Maternal Than Paternal Inheritance of Diabetes in GK Rats Diabetes ·Dominique Gauguier, Isabelle Nelson, Catherine Bernard, Véronique Parent, Cécile Marsac, Daniel Cohen, Philippe Froguel	1994	38
14	A new titinopathy Neurology ·Rafael de Cid, Rabah Ben Yaou, Carinne Roudaut, Karine Charton, Sylvain Baulande, France Leturcq, Norma B. Romero, Edoardo Malfatti, Maud Beuvin, Anna Vihola, Audrey Criqui, Isabelle Nelson, Juliette Nectoux, Laurène Ben Aim, Christophe Caloustian, Robert Olaso, Bjarne Udd, Gisèle Bonne, B. Eymard, (unknown)	2015	38
15	Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA ^Phe gene Neurology ·Gábor Zsurka, Kevin G. Hampel, Isabelle Nelson, Claude Jardel, Sandra R. Mirandola, Robert Sassen, Cornelia Kornblum, Pascale Marcorelles, Sébastien Lavoué, A. Lombès, Wolfram S. Kunz	2010	36
16	Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: Genetic, biochemical and morphological studies Journal of the Neurological Sciences ·Françoise Degoul, Isabelle Nelson, Patrick Lestienne, D. François, Norma B. Romero, D Duboc, B. Eymard, Michel Fardeau, G Ponsot, Marion Paturneau-Jouas, M Chaussain, J.P. Leroux, C. Marsac	1991	34
17	Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy Molecular Therapy — Nucleic Acids ·Fériel Azibani, Astrid Brull, Ludovic Arandel, Maud Beuvin, Isabelle Nelson, Arnaud Jollet, Esma Ziat, Bernard Prudhon, Sofia Benkhelifa‐Ziyyat, Marc Bitoun, Stéphanie Lorain, Gisèle Bonne, A. Bertrand	2017	32
18	Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution Journal of Neurology Neurosurgery & Psychiatry ·Nicolas Deconinck, Pascale Richard, Valérie Allamand, Anthony Béhin, Pascal Laforêt, Ana Ferreiro, Alix de Becdelièvre, C. Ledeuil, Corine Gartioux, Isabelle Nelson, R. Carlier, Pierre G. Carlier, Karim Wahbi, Norma B. Romero, M. T. Zabot, Françoise Bouhour, V. Tiffreau, (unknown), B. Eymard, Tanya Stojkovic	2014	32
19	Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases Cellular and Molecular Life Sciences ·Michael G. Hanna, Isabelle Nelson	1999	31
20	Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR Biochemical and Biophysical Research Communications ·B. Obermaier–Kusser, Josef Müller‐Höcker, Isabelle Nelson, Patrick Lestienne, C. Enter, Th. Riedele, Klaus-Dieter Gerbitz	1990	30

About Isabelle Nelson

Isabelle Nelson is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Genetics and Genetics, having authored 49 papers that have together received 1.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (26 papers), Metabolism and Genetic Disorders (20 papers), ATP Synthase and ATPases Research (11 papers), RNA Research and Splicing (8 papers), Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (6 papers), RNA modifications and cancer (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Clinical Biochemistry (565 citations), Molecular Biology (1.2k citations), Cellular and Molecular Neuroscience (232 citations), Neurology (69 citations) and Genetics (84 citations). Isabelle Nelson has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Michael G. Hanna, J A Morgan-Hughes, Nicholas Wood, A E Harding, Patrick Lestienne, Jonathan M. Cooper, Norma B. Romero, Shamima Rahman, C. Marsac and G Ponsot. Their work appears in journals such as Neuromuscular Disorders, Neurology, Journal of Neuromuscular Diseases, Journal of the Neurological Sciences and Biochemical and Biophysical Research Communications.

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