Ali Naini

9.6k citations

112 papers · 7.4k indexed · 1 hit paper · h-index 45

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Biochemistry top 0.2%
- Biochemical Acid Research Studies

Papers in

Clinical Biochemistry 31
- Metabolism and Genetic Disorders 31
Biochemistry 15
- Biochemical Acid Research Studies 13

Co-authors: Michio Hirano Salvatore DiMauro Serge Przedborski Vernice Jackson‐Lewis Catarina M. Quinzii Peter Teismann Du‐Chu Wu Kim Tieu
Journals: Neurology (11 papers)Journal of the Neurological Sciences (6 papers)Annals of Neurology (5 papers)Movement Disorders (3 papers)Journal of Child Neurology (3 papers)
Partner nations: United States Italy Germany

In The Last Decade

Ali Naini

110 papers receiving 7.2k citations

Hit Papers

align trajectories log scale

Cyclooxygenase-2 is instrumental in Parkinson's disease neurodegeneration 2003 · 546 citations

Peers

Countries citing papers authored by Ali Naini

Since Specialization

Citations

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

Fields of papers citing papers by Ali Naini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Phase I Randomized, Placebo-Controlled, Cross-Over Dose-Finding Study of Coenzyme Q10 on Doxorubicin Pharmacokinetics during Breast Cancer Treatment Integrative Cancer Therapies ·Heather Greenlee, Katherine D. Crew, Matthew Maurer, Kevin Kalinsky, Serge Cremers, Ali Naini, Wei Yann Tsai, Zaixing Shi, Frances Brogan, Dawn L. Hershman	2025	0
2	Genetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines Movement Disorders ·Jill Goldman, Wendy R. Uhlmann, Ali Naini, Robert Klitzman, Karen Marder	2023	3
3	Whole Exome Sequencing detects PYGM variants in two adults with McArdle disease Molecular Case Studies ·Amanda Thomas‐Wilson, Avinash V. Dharmadhikari, Jonas J. Heymann, Vaidehi Jobanputra, Salvatore DiMauro, Michio Hirano, Ali Naini, Mythily Ganapathi	2022	2
4	Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6 Journal of Neurology ·Andrés Berardo, Valentina Emmanuele, Wendy Vargas, Kurenai Tanji, Ali Naini, Michio Hirano	2019	15
5	Cerebellar Ataxia and CoQ10 Deficiency. PubMed Central ·Catarina M. Quinzii, Michio Hirano, Ali Naini	2013	4
6	Short Communication: Transplacental Nucleoside Analogue Exposure and Mitochondrial Parameters in HIV-Uninfected Children AIDS Research and Human Retroviruses ·Susan B. Brogly, Salvatore DiMauro, Russell B. Van Dyke, Paige L. Williams, Ali Naini, Daniel Libutti, Aborisade Titilope Abiola, Michelle Chung, Mariana Gerschenson	2010	30
7	Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNALeu(CUN) gene Journal of the Neurological Sciences ·Jorida Çoku, Sara Shanske, Chaste Uwihoreye, Kurenai Tanji, Ali Naini, Valentina Emmanuele, Marc C. Patterson, Michio Hirano, Salvatore DiMauro	2009	4
8	Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene Neuromuscular Disorders ·Belén Bornstein, Estela Área-Gómez, Kevin M. Flanigan, Jaya Ganesh, Parul Jayakar, Kathryn J. Swoboda, Jorida Çoku, Ali Naini, Sara Shanske, Kurenai Tanji, Michio Hirano, Salvatore DiMauro	2008	65
9	A novel tRNAVal mitochondrial DNA mutation causing MELAS Journal of the Neurological Sciences ·Kurenai Tanji, Petra Kaufmann, Ali Naini, Jiesheng Lu, István Lukács, Dong Wang, Joshua Z. Willey, Sara Shanske, Michio Hirano, Eduardo Bonilla, Alexander G. Khandji, Salvatore DiMauro, Lewis P. Rowland	2008	18
10	Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis Journal of the Neurological Sciences ·Ali Naini, Chaste Uwihoreye, Jiesheng Lu, Gordon Gilbert, Hiroshi Mitsumoto	2007	6
11	A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency The American Journal of Human Genetics ·Catarina M. Quinzii, Ali Naini, Leonardo Salviati, Eva Trevisson, Plácido Navas, Salvatore DiMauro, Michio Hirano	2006	263
12	Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations The American Journal of Human Genetics ·Luís C. López, Markus Schuelke, Catarina M. Quinzii, Tomotake Kanki, Richard J. Rodenburg, Ali Naini, Salvatore DiMauro, Michio Hirano	2006	299
13	Effect of Ezetimibe and/or Simvastatin on Coenzyme Q10 Levels in Plasma Drug Safety ·Heiner K. Berthold, Ali Naini, Salvatore Di Mauro, Maarit Hallikainen, Helena Gylling, Wilhelm Krone, Ioanna Gouni‐Berthold	2006	72
14	Sporadic amyotrophic lateral sclerosis and breast cancer: Hyaline conglomerate inclusions lead to identification of SOD1 mutation Journal of the Neurological Sciences ·Arthur P. Hays, Ali Naini, Abdullah Al Ahad, Hiroshi Mitsumoto, Lewis P. Rowland	2006	17
15	Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF Archives of Neurology ·Ali Naini, Jiesheng Lu, Petra Kaufmann, Richard A. Bernstein, Michelangelo Mancuso, Eduardo Bonilla, Michio Hirano, Salvatore DiMauro	2005	55
16	A Pathogenic Peripherin Gene Mutation in a Patient with Amyotrophic Lateral Sclerosis Brain Pathology ·Conrad L. Leung, Abdullah Al Ahad, Petra Kaufmann, Steven Chin, Ali Naini, Ronald K.H. Liem, Hiroshi Mitsumoto, Arthur P. Hays	2004	76
17	Atorvastatin Decreases the Coenzyme Q10 Level in the Blood of Patients at Risk for Cardiovascular Disease and Stroke Archives of Neurology ·Tatjana Rundek, Ali Naini, Ralph L. Sacco, Kristen Coates, Salvatore DiMauro	2004	155
18	D-β-Hydroxybutyrate rescues mitochondrial respiration and mitigates features of Parkinson disease Journal of Clinical Investigation ·Kim Tieu, Céline Perier, Casper Caspersen, Peter Teismann, Du‐Chu Wu, Shi-Du Yan, Ali Naini, Miquel Vila, Vernice Jackson‐Lewis, Ravichandran Ramasamy, Serge Przedborski	2003	357
19	Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis Journal of the Neurological Sciences ·Ali Naini, Olimpia Musumeci, Lindsay N. Hayes, Francesco Pallotti, Maura Del Bene, Hiroshi Mitsumoto	2002	4
20	Augmented pharmacologic stimulation of striatal acetylcholine release following developmental hypoxic-ischemic injury Brain Research ·Liu Le-xin, Ali Naini, Robert E. Burke	1996	3

About Ali Naini

Ali Naini is a scholar working on Clinical Biochemistry, Biochemistry, Neurology, Molecular Biology and Cellular and Molecular Neuroscience, having authored 112 papers that have together received 7.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (44 papers), Coenzyme Q10 studies and effects (31 papers), Metabolism and Genetic Disorders (31 papers), ATP Synthase and ATPases Research (21 papers), Advanced battery technologies research (20 papers), Biochemical Acid Research Studies (13 papers), Amyotrophic Lateral Sclerosis Research (12 papers) and Parkinson's Disease Mechanisms and Treatments (10 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Biochemistry (1.1k citations), Neurology (1.6k citations), Neurology (671 citations) and Cellular and Molecular Neuroscience (1.3k citations). Ali Naini has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Michio Hirano, Salvatore DiMauro, Serge Przedborski, Vernice Jackson‐Lewis, Catarina M. Quinzii, Peter Teismann, Du‐Chu Wu, Kim Tieu, Miquel Vila and Leonardo Salviati. Their work appears in journals such as Neurology, Journal of the Neurological Sciences, Annals of Neurology, Movement Disorders and Journal of Child Neurology.

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.

Explore authors with similar magnitude of impact