Chiara Rengo

5.2k total citations
22 papers, 1.9k citations indexed

About

Chiara Rengo is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Chiara Rengo has authored 22 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Clinical Biochemistry. Recurrent topics in Chiara Rengo's work include Mitochondrial Function and Pathology (8 papers), Forensic and Genetic Research (8 papers) and ATP Synthase and ATPases Research (6 papers). Chiara Rengo is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Forensic and Genetic Research (8 papers) and ATP Synthase and ATPases Research (6 papers). Chiara Rengo collaborates with scholars based in Italy, Spain and Germany. Chiara Rengo's co-authors include Antonio Torroni, Rosaria Scozzari, Daniele Sellitto, Ornella Semino, Alfredo Coppa, Alessandro Achilli, Fulvio Cruciani, A. Silvana Santachiara‐Benerecetti, Martin Richards and Vincent Macaulay and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Chiara Rengo

22 papers receiving 1.8k citations

Peers

Countries citing papers authored by Chiara Rengo

Since Specialization

Citations

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

Fields of papers citing papers by Chiara Rengo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Rengo

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop 2007 ·Journal of the Neurological Sciences ·(unknown), Cherubino Di Lorenzo, (unknown), Chiara Rengo, Alessio Cardinale, Mauro Racaniello, Filippo M. Santorelli, Giuseppe Nappi, Francesco Pierelli, Carlo Casali	21
2	The wolframin His611Arg polymorphism influences medication overuse headache 2007 ·Neuroscience Letters ·Cherubino Di Lorenzo, Grazia Sances, Giorgio Di Lorenzo, Chiara Rengo, Natascia Ghiotto, Elena Guaschino, Armando Perrotta, Filippo M. Santorelli, Giulio Grieco, Alfonso Troisi, Alberto Siracusano, Francesco Pierelli, Giuseppe Nappi, Carlo Casali	27
3	The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype 2006 ·Journal of Medical Genetics ·Maria Lucia Valentino, Piero Barboni, Chiara Rengo, Alessandro Achilli, Antonio Torroni, Raffaele Lodi, Caterina Tonon, Bruno Barbiroli, (unknown), (unknown), Agostino Baruzzi, Valério Carelli	21
4	Haplogroup Effects and Recombination of Mitochondrial DNA: Novel Clues from the Analysis of Leber Hereditary Optic Neuropathy Pedigrees 2006 ·The American Journal of Human Genetics ·Valério Carelli, Alessandro Achilli, Maria Lucia Valentino, Chiara Rengo, Ornella Semino, Maria Pala, Anna Olivieri, Marina Mattiazzi, Francesco Pallotti, Franco Carrara, Massimo Zeviani, Vincenzo Leuzzi, Carla Carducci, Giorgio Valle, Barbara Simionati, (unknown), Solange Rios Salomão, Rubens Belfort, Alfredo A. Sadun, Antonio Torroni	142
5	Saami and Berbers—An Unexpected Mitochondrial DNA Link 2005 ·The American Journal of Human Genetics ·Alessandro Achilli, Chiara Rengo, Vincenza Battaglia, Maria Pala, Anna Olivieri, Simona Fornarino, Chiara Magri, Rosaria Scozzari, Nora Babudri, A. Silvana Santachiara‐Benerecetti, Hans-Jürgen Bandelt, Ornella Semino, Antonio Torroni	171
6	The ND1 gene of complex I is a mutational hot spot for Leber’s hereditary optic neuropathy 2005 ·American Journal of Ophthalmology ·Maria Lucia Valentino, Piero Barboni, Anna Ghelli, (unknown), Chiara Rengo, Alessandro Achilli, Antonio Torroni, Alessandra Lugaresi, Raffaele Lodi, Bruno Barbiroli, Maria Teresa Dotti, Antonio Federico, Agostino Baruzzi, Valério Carelli	7
7	Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor 2004 ·The American Journal of Human Genetics ·Lluís Quintana‐Murci, Raphaëlle Chaix, R. Spencer Wells, Doron M. Behar, Hamid Sayar, Rosaria Scozzari, Chiara Rengo, Nadia Al-Zahery, Ornella Semino, A. Silvana Santachiara‐Benerecetti, Alfredo Coppa, Qasim Ayub, Aisha Mohyuddin, Chris Tyler‐Smith, S. Qasim Mehdi, Antonio Torroni, Ken McElreavey	317
8	The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy 2004 ·Annals of Neurology ·Maria Lucia Valentino, Piero Barboni, Anna Ghelli, (unknown), Chiara Rengo, Alessandro Achilli, Antonio Torroni, Alessandra Lugaresi, Raffaele Lodi, Bruno Barbiroli, M. T. Dotti, Antonio Federico, Agostino Baruzzi, Valério Carelli	93
9	Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation 2003 ·The American Journal of Human Genetics ·Antonio Torroni, Yolanda Campos, Chiara Rengo, Daniele Sellitto, Alessandro Achilli, Chiara Magri, Ornella Semino, Alberto García‐Redondo, (unknown), Joaquı́n Arenas, Rosaria Scozzari	47
10	Identification of Native American Founder mtDNAs Through the Analysis of Complete mtDNA Sequences: Some Caveats 2003 ·Annals of Human Genetics ·H-J Bandelt, Corinna Herrnstadt, Yong‐Gang Yao, Qing‐Peng Kong, Toomas Kivisild, Chiara Rengo, Rosaria Scozzari, Martin Richards, Richard Villems, Vincent Macaulay, Neil Howell, Antonio Torroni, Yong Zhang	85
11	Extensive Female-Mediated Gene Flow from Sub-Saharan Africa into Near Eastern Arab Populations 2003 ·The American Journal of Human Genetics ·Martin Richards, Chiara Rengo, Fulvio Cruciani, Fiona Gratrix, James F. Wilson, Rosaria Scozzari, Vincent Macaulay, Antonio Torroni	95
12	Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy 2002 ·Annals of Neurology ·Maria Lucia Valentino, Patrizia Avoni, Piero Barboni, Francesco Pallotti, Chiara Rengo, Antonio Torroni, Marzio Bellan, Agostino Baruzzi, Valério Carelli	39
13	Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy 2002 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Valério Carelli, Lodovica Vergani, (unknown), (unknown), (unknown), Maria Lucia Valentino, Chiara Rengo, Antonio Torroni, Andrea Martinuzzi	54
14	Do the Four Clades of the mtDNA Haplogroup L2 Evolve at Different Rates? 2001 ·The American Journal of Human Genetics ·Antonio Torroni, Chiara Rengo, Valentina Guida, Fulvio Cruciani, Daniele Sellitto, Alfredo Coppa, Fernando Luna Calderón, Barbara Simionati, Giorgio Valle, Martin Richards, Vincent Macaulay, Rosaria Scozzari	165
15	Intervertebral disc lesions in diffuse idiopathic skeletal hyperostosis (DISH). 2001 ·PubMed ·C. Di Girolamo, N. Pappone, Chiara Rengo, (unknown), C. Crisci, Ignazio Olivieri	8
16	Phylogeography of the human mitochondrial haplogroup L3e: a snapshot of African prehistory and Atlantic slave trade. 2001 ·PubMed ·H.-J. Bandelt, Juliana Alves‐Silva, Pedro Edson Moreira Guimarães, Magda Santos, António Brehm, Luı́sa Pereira, Alfredo Coppa, J. M. Larruga, Chiara Rengo, Rosaria Scozzari, Antonio Torroni, Maria João Prata, António Amorim, Vânia F. Prado, Sérgio D.J. Pena	65
17	Phylogeography of the human mitochondrial haplogroup L3e: a snapshot of African prehistory and Atlantic slave trade 2001 ·Annals of Human Genetics ·H. -J. Bandelt, Juliana Alves‐Silva, Pedro Edson Moreira Guimarães, Magda Santos, António Brehm, Luı́sa Pereira, Alfredo Coppa, J. M. Larruga, Chiara Rengo, Rosaria Scozzari, Antonio Torroni, Maria João Prata, António Amorim, Vânia F. Prado, Sérgio D.J. Pena	58
18	The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness 1999 ·The American Journal of Human Genetics ·Antonio Torroni, Fulvio Cruciani, Chiara Rengo, Daniele Sellitto, Núria López-Bigas, Raquel Rabionet, Nancy Govea, Adolfo López de Munaín, (unknown), Lourdes Romero, Manuela Villamar, Ignacio del Castillo, Felipe Moreno, Xavier Estivill, Rosaria Scozzari	91
19	mtDNA Analysis Reveals a Major Late Paleolithic Population Expansion from Southwestern to Northeastern Europe 1998 ·The American Journal of Human Genetics ·Antonio Torroni, Hans‐Jürgen Bandelt, (unknown), Päivi Lahermo, Pedro Moral, Daniele Sellitto, Chiara Rengo, Peter Forster, Marja‐Liisa Savontaus, Batsheva Bonné‐Tamir, Rosaria Scozzari	286
20	Ossification of the posterior longitudinal ligament in one of a pair of identical twins concordant for ankylosing spondylitis 1994 ·Clinical Rheumatology ·Ignazio Olivieri, N. Pappone, Angela Padula, Chiara Rengo, (unknown), (unknown), (unknown), S. Ferri, G Pasero	6

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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