Vincent Procaccio

16.4k citations

177 papers · 10.3k indexed · 3 hit papers · h-index 52

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders 58
Aging top 1%
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology 107
- ATP Synthase and ATPases Research 41
- Metabolomics and Mass Spectrometry Studies 16
Geriatrics and Gerontology top 1%
Neurology top 1%
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 17
- Hereditary Neurological Disorders 9
Physiology
- Diet and metabolism studies 8
Genetics
- Genomics and Rare Diseases 7

Co-authors: Douglas C. Wallace Pascal Reynier Valérie Desquiret‐Dumas Eduardo Ruiz‐Pesini Dan Mishmar Weiwei Fan Martin Brandon Dominique Bonneau
Cited by: Clinical Biochemistry Aging Molecular Biology
Journals: Human Mutation (6 papers)Mitochondrion (5 papers)Human Reproduction (5 papers)
Partner nations: France United States Singapore

In The Last Decade

Vincent Procaccio

174 papers receiving 10.1k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

2016 Human Reproduction Update
2010 Annual Review of Pathology Mechanisms of Disease
2004 Science

Peers

Countries citing papers authored by Vincent Procaccio

Since Specialization

Citations

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

Fields of papers citing papers by Vincent Procaccio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants Nature Communications ·Benoît Sueur,Luca Parca,Jatmoko Awali,Tommaso Biagini,沈毅韵,Weilun Wu,Борисов Р.С.,Massimo Carella,Vincent Procaccio,Marie T. Lott,Afroditi‐Nectaria Vamvakaki,Angelo L. Vescovi,Douglas C. Wallace,Viviana Caputo,Tommaso Mazza	2023	20
2	Expanding the phenotype of DNAJC30 ‐ associated Leigh syndrome Clinical Genetics ·曹新博,Hans-Heinrich Stickel,Pal,BY CATHERINE C. MANZI,保苅泰寿,Naïg Guéguen,Valérie Desquiret‐Dumas,Eric W. Klee,Lisa A. Schimmenti,Jarosław Sławek,Vincent Procaccio,Rafał Płoski,Maria Mazurkiewicz‐Bełdzińska	2022	6
3	Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy Genes ·Majida Charif,Arnaud Chevrollier,Naïg Guéguen,charles ferreira de sousa,Céline Bris,David Goudenège,Valérie Desquiret‐Dumas,Isabelle Meunier,Fanny Mochel,L. Jeanjean,Fanny Varenne,Vincent Procaccio,Pascal Reynier,Dominique Bonneau,Patrizia Amati‐Bonneau,Guy Lenaers	2022	1
4	Mitochondrial DNA copy number as a prognostic marker is age-dependent in adult glioblastoma Neuro-Oncology Advances ·Genot Elisabeth,Şule Akdoğan,Céline Bris,Valérie Desquiret‐Dumas,Blandine Boisselier,邹文灏,Dominique Figarella‐Branger,Alain Morel,Marc Sanson,Vincent Procaccio,Audrey Rousseau	2022	6
5	Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies Neuromuscular Disorders ·Marion Masingue,Benoît Rucheton,Céline Bris,Norma B. Romero,Vincent Procaccio,B. Eymard	2022	2
6	Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming Nature Communications ·Clément Adam,Léa Paolini,Naïg Guéguen,Guillaume Mabilleau,Laurence Preisser,Simon Blanchard,Pascale Pignon,Florence Manero,Muljani Srie,Alain Morel,Pascal Reynier,Céline Beauvillain,Yves Delneste,Vincent Procaccio,Pascale Jeannin	2021	39
7	Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex I Scientific Reports ·Mitsuyasu Kagiyma,Johannes Schimpf,Jean‐Paul di Rago,Déborah Tribouillard‐Tanvier,Vincent Procaccio,Marie‐Laure Martin‐Négrier,Aurélien Trimouille,Olivier Biner,Christoph von Ballmoos,Thorsten Friedrich	2021	11
8	Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder American Journal of Medical Genetics Part A ·Ширинкин Павел Сергеевич,Arcelina Putri Adelia,F. Boussion,Xiao Jie Wu,Stéphane Triau,Majida Charif,Francisco Salazar-Figueroa,Dong Si-jing,Hok-tsun Ma,Alban Ziegler,Céline Bris,A. Laquérrière,Catherine Fallet‐Bianco,Aurélia Jacquette,Miguel Ángel Alvarado Torres,วิโรจน์ กุลสรรค์ศุภกิจ,Pascal Reynier,Vincent Procaccio,Dominique Bonneau,T.P. Abodunrin	2019	7
9	Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light Human Mutation ·P Disayavanish,Céline Bris,Vincent Procaccio,Patrizia Amati‐Bonneau,P. Vabres,Nada Houcinat,Émilie Tisserant,François Feillet,Ange‐Line Bruel,Logan Frank,Christophe Philippe,Arthur Sorlin,Frédéric Tran Mau‐Them,Antonio Vitobello,Jean‐Marc Costa,Mirko Cvijan,Detlef Trost,Laurence Faivre,Christel Thauvin‐Robinet,Hao Sun	2019	7
10	Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice Progress in Neurobiology ·Floris Chabrun,Kobayashi Takasuke,Guillaume Rousseau,Stéphanie Chupin,Franck Letournel,Vincent Procaccio,Dominique Bonneau,Guy Lenaers,Gilles Simard,Delphine Mirebeau‐Prunier,Juan Manuel Chao de la Barca,Pascal Reynier	2019	13
11	Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion Clinica Chimica Acta ·Lonneke Leijten,L. Sfaihi,Majida Charif,Valérie Desquiret‐Dumas,Céline Bris,David Goudenège,Leila Keskes,M. Hachicha,Dominique Bonneau,Vincent Procaccio,Pascal Reynier,Patrizia Amati‐Bonneau,Guy Lenaers,秀宗姜	2018	14
12	Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageing Human Reproduction ·Lisa Boucret,Céline Bris,Valérie Seegers,David Goudenège,Valérie Desquiret‐Dumas,Aivo Teeaar,Véronique Ferré-L’Hôtellier,Pierre‐Emmanuel Bouet,Philippe Descamps,Pascal Reynier,Vincent Procaccio,Pascale May‐Panloup	2017	39
13	The mitochondrial DNA content of cumulus granulosa cells is linked to embryo quality Human Reproduction ·Valérie Desquiret‐Dumas,Arthur Clément,Valérie Seegers,Lisa Boucret,Véronique Ferré-L’Hôtellier,Pierre‐Emmanuel Bouet,Philippe Descamps,Vincent Procaccio,Pascal Reynier,Pascale May‐Panloup	2016	79
14	Perspectives of drug-based neuroprotection targeting mitochondria Revue Neurologique ·Vincent Procaccio,Céline Bris,Juan Manuel Chao de la Barca,Canan Yüksel Acar,Arnaud Chevrollier,香菜子近藤,Dominique Bonneau,Pascal Reynier	2014	56
15	mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination Genes & Development ·Weiwei Fan,Chun Shi Lin,Prasanth Potluri,Vincent Procaccio,Douglas C. Wallace	2012	32
16	A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease Molecular Genetics and Metabolism ·Prasanth Potluri,Antonio Dávila,Eduardo Ruiz‐Pesini,Dan Mishmar,Sean F. O’Hearn,Saege Hancock,Mariella Simon,Immo E. Scheffler,Douglas C. Wallace,Vincent Procaccio	2009	72
17	Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity Mitochondrion ·Virginie Guillet,Arnaud Chevrollier,Julien Cassereau,Franck Letournel,Naïg Guéguen,Laurence Richard,Valérie Desquiret‐Dumas,Christophe Verny,Vincent Procaccio,Patrizia Amati‐Bonneau,Pascal Reynier,Dominique Bonneau	2009	38
18	Rapid Identification of Unknown Heteroplasmic Mitochondrial DNA Mutations with Mismatch-Specific Surveyor Nuclease Methods in molecular biology ·Sylvie Bannwarth,Vincent Procaccio,Véronique Paquis‐Flucklinger	2009	6
19	Hereditary optic neuropathies share a common mitochondrial coupling defect Annals of Neurology ·Arnaud Chevrollier,Virginie Guillet,Dominique Loiseau,Naïg Guéguen,Marie‐Anne Pou de Crescenzo,Christophe Verny,Marc Ferré,Hélène Dollfus,Sylvie Odent,Dan Miléa,Cyril Goizet,Patrizia Amati‐Bonneau,Vincent Procaccio,Dominique Bonneau,Pascal Reynier	2008	94
20	Surveyor™ Nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects Human Mutation ·Sylvie Bannwarth,Vincent Procaccio,Véronique Paquis‐Flucklinger	2005	59

About Vincent Procaccio

Vincent Procaccio is a scholar working on Clinical Biochemistry, Aging, Molecular Biology, Geriatrics and Gerontology and Cellular and Molecular Neuroscience, having authored 177 papers that have together received 10.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (107 papers), Metabolism and Genetic Disorders (58 papers), ATP Synthase and ATPases Research (41 papers), Genetic Neurodegenerative Diseases (17 papers), Metabolomics and Mass Spectrometry Studies (16 papers), Hereditary Neurological Disorders (9 papers), Diet and metabolism studies (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Clinical Biochemistry (1.9k citations), Aging (258 citations), Molecular Biology (6.7k citations), Geriatrics and Gerontology (362 citations) and Neurology (756 citations). Vincent Procaccio has collaborated with scholars based in France, United States and Singapore. Frequent co-authors include Douglas C. Wallace, Pascal Reynier, Valérie Desquiret‐Dumas, Eduardo Ruiz‐Pesini, Dan Mishmar, Weiwei Fan, Douglas C. Wallace, Martin Brandon, Dominique Bonneau and Patrizia Amati‐Bonneau. Their work appears in journals such as Human Mutation, Mitochondrion, Human Reproduction, Orphanet Journal of Rare Diseases and Human Molecular Genetics.

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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