Djamel Grid

2.4k citations

32 papers · 1.9k · h-index 20

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 25
- Hereditary Neurological Disorders 23
- Genetic Neurodegenerative Diseases 4
Neurology 9
- Neurological diseases and metabolism 9

Co-authors: Mériem Tazir (11 shared papers)Nicolas Lévy (8 shared papers)T. Hammadouche (4 shared papers)Malika Chaouch (2 shared papers)Annachiara De Sandre‐Giovannoli (4 shared papers)Jean-Michel Vallat (3 shared papers)Serguei V. Kozlov (2 shared papers)Pierre Szepetowski (2 shared papers)
Journals: Neuromuscular Disorders (7 papers)Neurology (3 papers)The American Journal of Human Genetics (3 papers)Annals of Neurology (2 papers)Journal of the Neurological Sciences (1 paper)
Partner nations: France Algeria Switzerland

In The Last Decade

Djamel Grid

32 papers receiving 1.8k citations

Peers

Countries citing papers authored by Djamel Grid

Since Specialization

Citations

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

Fields of papers citing papers by Djamel Grid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Djamel Grid, 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 Djamel Grid Line = papers co-authored together Djamel Grid 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 32 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse The American Journal of Human Genetics ·Annachiara De Sandre‐Giovannoli, Malika Chaouch, Serguei V. Kozlov, Jean-Michel Vallat, Mériem Tazir, Nadia Kassouri, Pierre Szepetowski, T. Hammadouche	2002	457
2	Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum Nature Genetics ·Giovanni Stévanin, Filippo Maria Santorelli, Hamid Azzedine, Paula Coutinho, Jacques Chomilier, Paola S. Denora, Elodie Martin, Anne Marie Ouvrard-Hernandez	2007	278
3	Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H The American Journal of Human Genetics ·Valérie Delague, Arnaud Jacquier, Tarik Hamadouche, Yannick Poitelon, Cécile Baudot, Irène Boccaccio, Éliane Chouery, Malika Chaouch	2007	129
4	Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q Annals of Neurology ·Juan José Poza, A. S�enz, A. Mart�nez-Gil, N. Cheron, Ana María Cobo, Miguel Urtasun, J. F. Mart�-Mass�, Djamel Grid	1999	117
5	CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5 Brain ·Cyril Goizet, A. Boukhris, A. Dürr, Christian Beetz, Jérémy Truchetto, Christelle Tesson, Maria K. Tsaousidou, Sylvie Forlani	2009	92
6	Mutation analysis of the paraplegin gene ( SPG7 ) in patients with hereditary spastic paraplegia Neurology ·Nour Elleuch, Christel Depienne, Ali Benomar, Angel Hernandez, Xavier Cano Ferrer, Bertrand Fontaine, Djamel Grid, Chantal M E Tallaksen	2006	87
7	The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene Neuromuscular Disorders ·M. Chaouch, Y. Allal, Annachiara De Sandre‐Giovannoli, J.M. Vallat, A. Amer-el-Khedoud, Nora Kassouri, Amina Chaouch, Philippe Sindou	2002	78
8	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene Archives of Neurology ·Amets Sáenz, Juan Carlos Galán, Christophe Caloustian, Frédéric Lorenzo, Celedonio Márquez, Núria Rodríguez, María Dolores Jiménez, Juan José Poza	1999	75
9	Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias Archives of Neurology ·Paula Coutinho, José Hugo da Silva Barros, R. Zemmouri, Joás Guimarães, Cristina Alves, Riu Chorão, Esmeralda Lourenço, Paula Ribeiro	1999	73
10	A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot‐Marie‐Tooth disease Neurology ·M. Kessali, R. Zemmouri, A. Guilbot, Thierry Maisonobe, Alexis Brice, Éric Leguern, Djamel Grid	1997	66
11	A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset The American Journal of Human Genetics ·Maria D. Lalioti, Hamish S. Scott, Pierre Genton, Djamel Grid, Réda Ouazzani, Amel Mrabet, Riadh Gouider, Charlotte Dravet	1998	59
12	Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients Journal of the Neurological Sciences ·Mériem Tazir, Lamia Alipacha, A. M’zahem, Jean‐Pierre Delaunoy, M. Fritsch, Sonia Nouioua, Traki Benhassine, Salima Assami	2009	52
13	Phenotypic variability in giant axonal neuropathy Neuromuscular Disorders ·Mériem Tazir, Sonia Nouioua, Laurent Magy, Kathrin Huehne, Salima Assami, Andoni Urtizberea, Djamel Grid, Tarik Hamadouche	2009	45
14	The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa Neurology ·Pascale Richard, Karen Gaudon, Majed Haddad, Asma Ben Ammar, Emmanuelle Génin, Stéphanie Bauché, Marion Paturneau-Jouas, Juliane S. Müller	2008	36
15	Autosomal-Recessive Charcot-Marie-Tooth Diseases Journal of Neuropathology & Experimental Neurology ·Jean-Michel Vallat, Mériem Tazir, Corinne Magdelaine, Franck G. Sturtz, Djamel Grid	2005	34
16	Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy Neuromuscular Disorders ·R. Zemmouri, Hamid Azzedine, Salima Assami, N. Kitouni, Jean‐Michel Vallat, Thierry Maisonobe, Tarik Hamadouche, M. Kessaci	2000	33
17	Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME Epilepsy Research ·Tom Moore, Stéphane Hecquet, Andrew McLellann, Dorothee M. Ville, Djamel Grid, Fabienne Picard, Bruno Moulard, Philip J. Asherson	2001	31
18	Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1 Neuromuscular Disorders ·Mériem Tazir, Jean-Michel Vallat, Pascale Bomont, R. Zemmouri, Philippe Sindou, Salima Assami, Sonia Nouioua, T. Hammadouche	2002	23
19	Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa Annals of Human Genetics ·Tarik Hamadouche, Yannick Poitelon, Emmanuelle Génin, M. Chaouch, M. Tazir, Nora Kassouri, Sonia Nouioua, Amina Chaouch	2008	22
20	Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes Neuromuscular Disorders ·Sonia Nouioua, Tarik Hamadouche, Benoît Funalot, Rafaëlle Bernard, Nora Bellatache, Radia Bouderba, Djamel Grid, Salima Assami	2011	22

About Djamel Grid

Djamel Grid is a scholar working on Cellular and Molecular Neuroscience, Neurology, Cell Biology, Rheumatology and Neurology, having authored 32 papers that have together received 1.9k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (23 papers), Neurological diseases and metabolism (9 papers), RNA regulation and disease (5 papers), Nuclear Structure and Function (5 papers), Cellular Mechanics and Interactions (5 papers), RNA Research and Splicing (5 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Genetic Neurodegenerative Diseases (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (465 citations), Neurology (327 citations), Genetics (228 citations) and Cell Biology (326 citations). Djamel Grid has collaborated with scholars based in France, Algeria and Switzerland. Frequent co-authors include Mériem Tazir, Nicolas Lévy, T. Hammadouche, Malika Chaouch, Annachiara De Sandre‐Giovannoli, Jean-Michel Vallat, Serguei V. Kozlov, Pierre Szepetowski, Colin L. Stewart and Antoon Vandenberghe. Their work appears in journals such as Neuromuscular Disorders, Neurology, The American Journal of Human Genetics, Annals of Neurology and Journal of the Neurological Sciences.

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