Laura Jarre

514 total citations
18 papers, 385 citations indexed

About

Laura Jarre is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Laura Jarre has authored 18 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Laura Jarre's work include Muscle Physiology and Disorders (7 papers), Genetic Neurodegenerative Diseases (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Laura Jarre is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Genetic Neurodegenerative Diseases (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Laura Jarre collaborates with scholars based in Italy, United States and Norway. Laura Jarre's co-authors include Marina Mora, Claudia Di Blasi, Lucía Morandi, Rita Barresi, Carlo Antozzi, F. Cornelio, Antonella Pini, Anu Suomalainen, Massimo Zeviani and Renato Mantegazza and has published in prestigious journals such as Neurology, Annals of Neurology and Acta Neuropathologica.

In The Last Decade

Laura Jarre

18 papers receiving 376 citations

Peers

Countries citing papers authored by Laura Jarre

Since Specialization

Citations

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

Fields of papers citing papers by Laura Jarre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Jarre

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Jarre. A scholar is included among the top collaborators of Laura Jarre 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 Laura Jarre. Laura Jarre is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Cognitive evolution of a girl submitted to right hemispherotomy when five years old 2009 ·Brain and Development ·Piernanda Vigliano, (unknown), Irene Bagnasco, Laura Jarre	8
2	LAMA2 stop-codon mutation: Merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression 2008 ·European Journal of Paediatric Neurology ·Piernanda Vigliano, (unknown), Claudia Di Blasi, Marina Mora, Laura Jarre	23
3	Danon disease: A novel LAMP2 mutation affecting the pre-mRNA splicing and causing aberrant transcripts and partial protein expression 2008 ·Neuromuscular Disorders ·Claudia Di Blasi, Laura Jarre, Flavia Blàsevich, (unknown), Marina Mora	13
4	LAMA2 Gene Analysis in Congenital Muscular Dystrophy 2005 ·Archives of Neurology ·Claudia Di Blasi, Daniela Piga, (unknown), Isabella Moroni, Antonella Pini, Alessandra Ruggieri, Simona Zanotti, Graziella Uziel, Laura Jarre, Elvio Della Giustina, Carmela Scuderi, Christoffer Jonsrud, Renato Mantegazza, Lucía Morandi, Marina Mora	24
5	Hair anomalies as a sign of mitochondrial disease 2003 ·European Journal of Pediatrics ·Margherita Silengo, Mariella Valenzise, Marco Spada, Giovanni Battista Ferrero, Silvio Ferraris, (unknown), Laura Jarre	13
6	Manganese Intoxication: The Cause of an Inexplicable Epileptic Syndrome in a 3 Year Old Child 2003 ·NeuroToxicology ·Elena Herrero Hernández, G Discalzi, (unknown), Laura Jarre, Enrico Pira	27
7	A somatic and germline mosaic mutation in MPZ/P ₀ mimics recessive inheritance of CMT1B 2001 ·Neurology ·Gian Maria Fabrizi, Moreno Ferrarini, Tiziana Cavallaro, Laura Jarre, A. Polo, N. Rizzuto	22
8	Gonosomal Mosaicism Of A Novel Heterozygous Mutation Of P Causes Charcot‐Marie‐Tooth Neuropathy Type 1b With Apparent Autosomal Recessive Inheritance 2001 ·Journal of the Peripheral Nervous System ·G Fabrizi, Moreno Ferrarini, Tiziana Cavallaro, Federica Taioli, A. Polo, Laura Jarre, N. Rizzuto	1
9	New clinical findings in oculo-ecNew clinical findings in oculo-ectodermal syndrome. 2000 ·Clinical Dysmorphology ·Margherita Silengo, Margherita Lerone, Marco Seri, Manuela Priolo, Laura Jarre	3
10	Homogeneous phenotype of the gypsy limb-girdle MD with the γ-sarcoglycan C283Y mutation 2000 ·Neurology ·Luciano Merlini, (unknown), Carmen Navarro, A Barois, Dominique Bonneau, (unknown), Bernard Échenne, P. Gallano, Laura Jarre, Marc Jeanpierre, Luba Kalaydjieva, France Leturcq, (unknown), Annick Toutain, Ivailo Tournev, Andoni Urtizberea, Jean‐Michel Vallat, Thomas Voït, J Warter	42
11	New clinical findings in oculo-ectodermal syndrome 2000 ·Clinical Dysmorphology ·Margherita Silengo, Margherita Lerone, Marco Seri, Manuela Priolo, Laura Jarre	8
12	Trichorrhexis Nodosa and lip pits in autosomal dominant ectodermal dysplasia—central nervous system malformation syndrome 1997 ·American Journal of Medical Genetics ·Margherita Silengo, (unknown), Laura Jarre	5
13	Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects 1997 ·Acta Neuropathologica ·Rita Barresi, (unknown), (unknown), Claudia Di Blasi, E Torchiana, Renato Mantegazza, Laura Jarre, Nardo Nardocci, P Boffi, Frediano Tezzon, Antonella Pini, F. Cornelio, Marina Mora, Lucía Morandi	39
14	Developmental expression of dystrophin, dystrophin-associated glycoproteins and other membrane cytoskeletal proteins in human skeletal and heart muscle 1996 ·Developmental Brain Research ·Marina Mora, Claudia Di Blasi, Rita Barresi, Lucía Morandi, B. Brambati, Laura Jarre, F. Cornelio	30
15	Clinical heterogeneity of adhalin deficiency 1996 ·Annals of Neurology ·Lucía Morandi, Rita Barresi, Claudia Di Blasi, Daniel Jung, Yoshihide Sunada, (unknown), F. Dworzak, Renato Mantegazza, Carlo Antozzi, Laura Jarre, Antonella Pini, Giuseppe Gobbi, C Bíanchi, F. Cornelio, Kevin P. Campbell, Marina Mora	15
16	Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA 1995 ·Journal of Neurology ·Caterina Mariotti, (unknown), Anu Suomalainen, Marco Rimoldi, Giacomo P. Comi, A. Prelle, Carlo Antozzi, Serenella Servidei, Laura Jarre, Stefano DiDonato, Massimo Zeviani	80
17	Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype 1995 ·Journal of the Neurological Sciences ·Lucía Morandi, Marina Mora, (unknown), Rita Barresi, Claudia Di Blasi, Raffaella Brugnoni, Pia Bernasconi, Renato Mantegazza, F. Dworzak, Carlo Antozzi, María Balestrini, Laura Jarre, Antonella Pini, Luciano Merlini, G. Piccolo, (unknown), (unknown), Flavia Blàsevich, F. Cornelio	31
18	[Cerebral and renal morphological malformations in a subject with suspected fetal alcoholic syndrome. Case report]. 1979 ·PubMed ·(unknown), Paola Bini, Laura Jarre, Francesco Basile	1

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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