I. Ceballos

898 citations

21 papers · 587 indexed · h-index 15

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Biochemistry top 10%

Papers in

Clinical Biochemistry 5
- Metabolism and Genetic Disorders 5
Nephrology 2

Co-authors: Annie Nicole P. Kamoun P.-M. Sinet A. Défossez André Delacourte Paul Jungers Pierre‐Marie Sinet Philippe Chauveau
Journals: Journal of Inherited Metabolic Disease (2 papers)Kidney International (2 papers)Clinica Chimica Acta (1 paper)Advances in experimental medicine and biology (1 paper)European Journal of Medical Genetics (1 paper)
Partner nations: France Belgium

In The Last Decade

I. Ceballos

21 papers receiving 571 citations

Peers

Countries citing papers authored by I. Ceballos

Since Specialization

Citations

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

Fields of papers citing papers by I. Ceballos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside I. Ceballos, 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 I. Ceballos Line = papers co-authored together I. Ceballos 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	ATP7A mutation with occipital horns and distal motor neuropathy: A continuum European Journal of Medical Genetics ·Mélanie Fradin, Alinoë Lavillaureix, Sylvie Jaillard, Chloé Quēlin, Paul Sauleau, Katsumi Enomoto, Dominique Ménard, Gilles Edan, I. Ceballos, Catherine Tréguier, Maïa Proisy, Corinne Magdelaine, Anne‐Sophie Lia, Sylvie Odent, Laurent Pasquier	2020	8
2	AICA‐ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long‐term update on the first case Journal of Inherited Metabolic Disease ·Francis Ramond, Marlène Rio, Bénédicte Héron, Apolline Imbard, Sandrine Marie, Kareen Billiemaz, Anne‐Sophie Denommé‐Pichon, Paul Kuentz, I. Ceballos, Monique Piraud, Marie‐Françoise Vincent, Renaud Touraine	2020	26
3	Aromatic L-Amino Acid Decarboxylase Deficiency Is a Cause of Long-Fasting Hypoglycemia The Journal of Clinical Endocrinology & Metabolism ·木戸健治, Léna Damaj, Herton Viana Correia, Valérie Serre, Laurence Hubert, 正治矢部, Gilles Simard, I. Ceballos, Laurence Christa, Pascale de Lonlay	2013	22
4	Homocyst(e)ine, oxidative stress, and endothelium function in uremic patients Kidney International ·Ziad A. Massy, I. Ceballos, Deresse Mersha, Thao Nguyen‐Khoa, Béatrice Descamps‐Latscha, Tilman B. Drüeke, Paul Jungers	2001	23
5	Homocyst(e)ine, oxidative stress, and endothelium function in uremic patients Kidney International ·Ziad A. Massy, I. Ceballos, Deresse Mersha, Thao Nguyen‐Khoa, Béatrice Descamps‐Latscha, Tilman B. Drüeke, Paul Jungers	2001	8
6	Premature thymic involution, observed at the ultrastructural level, in two lineages of human-SOD-1 transgenic mice Mechanisms of Ageing and Development ·B Nabarra, M Casanova, Daniel Paris, Evelyne Paly, Sherlin Tazkiya Nur Salsabila, I. Ceballos, Jacqueline London	1997	14
7	Transgenic mice overexpressing the human Cu/Zn-SOD gene: ultrastructural studies of a premature thymic involution model of Down's syndrome (trisomy 21). PubMed ·B Nabarra, M Casanova, Daniel Paris, Annie Nicole, Keiko Toyama, J. Scott, I. Ceballos, Jacqueline London	1996	24
8	CASE REPORT Lesch-Nyhan syndrome in a girl Patrick Van Bogaert, I. Ceballos, Isabelle Desguerre, Louise Telvi, P. Kamoun, G Ponsot	1992	1
9	Lesch‐Nyhan syndrome in a girl Journal of Inherited Metabolic Disease ·Patrick Van Bogaert, I. Ceballos, Isabelle Desguerre, Louise Telvi, P. Kamoun, G Ponsot	1992	16
10	Expression of Human Cu-Zn Superoxide Dismutase Gene in Transgenic Mice: Model for Gene Dosage Effect in Down Syndrome Free Radical Research Communications ·I. Ceballos, Annie Nicole, Pascale Briand, G Grimber, A. Delacourte, Stéphane Flament, Jean‐Louis Blouin, M. Thévenin, P. Kamoun, P.-M. Sinet	1991	32
11	Neuronal Localization of Copper-Zinc Superoxide Dismutase Protein and mRNA within the Human Hippocampus from Control and Alzheimer'S Disease Brains Free Radical Research Communications ·I. Ceballos, F. Javoy‐Agid, A. Delacourte, A. Défossez, Monique Lafon, Étienne C. Hirsch, Annie Nicole, P.-M. Sinet, Yves Agid	1991	32
12	Parkinson’s Disease and Alzheimer’s Disease :Neurodegenerative Disorders Due to Brain Antioxidant System Deficiency ? Advances in experimental medicine and biology ·I. Ceballos, France Javoy‐Agid, André Delacourte, A. Défossez, Annie Nicole, Büşra Nur Daşkıran	1990	20
13	Early alterations of plasma free amino acids in chronic renal failure Clinica Chimica Acta ·I. Ceballos, Philippe Chauveau, Valérie Guérin, J Bardet, P Parvy, P. Kamoun, Paul Jungers	1990	89
14	Localization of copper-zinc superoxide dismutase mRNA in human hippocampus by in situ hybridization Neuroscience Letters ·I. Ceballos, France Javoy‐Agid, Étienne C. Hirsch, Sylvie Dumas, P. Kamoun, P.-M. Sinet, Yves Agid	1989	18
15	Expression of transfected human CuZn superoxide dismutase gene in mouse L cells and NS20Y neuroblastoma cells induces enhancement of glutathione peroxidase activity Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·I. Ceballos, Jean‐Maurice Delabar, Annie Nicole, Thomas Michael Speidel, Robert A. Hallewell, P. Kamoun, P.-M. Sinet	1988	80
16	Preferential localization of copper zinc superoxide dismutase in the vulnerable cortical neurons in Alzheimer's disease Neuroscience Letters ·André Delacourte, A. Défossez, I. Ceballos, Annie Nicole, Pierre‐Marie Sinet	1988	71
17	Trisomie 21 et maladie d'Alzheimer médecine/sciences ·Āśisha Kumāra Rāuta, O Chaallal, I. Ceballos, Jordan Caminiti	1987	3
18	Cystathionine beta synthase: Gene dosage effect in trisomy 21 Biochemical and Biophysical Research Communications ·B. Chadefaux, M O Rethoré, O Raoul, I. Ceballos, M Poissonnier, С.С. Корецкая, Delphine Allard	1985	79
19	[Effects of gene localization and its metabolic significance in trisomy 21]. PubMed ·H Jérôme, B. Chadefaux, I. Ceballos, Delphine Allard	1985	2
20	[The effects of cerebral ischemia on the level of metabolites of dopamine and serotonin in the rat cerebrospinal fluid]. PubMed ·I. Ceballos, Dominique Laude, Aarushi Nargas, A. Ender Ersin	1984	2

About I. Ceballos

I. Ceballos is a scholar working on Clinical Biochemistry, Nephrology, Physiology, Neurology and Physiology, having authored 21 papers that have together received 587 indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (6 papers), Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers), Down syndrome and intellectual disability research (2 papers), Trace Elements in Health (2 papers), Cholinesterase and Neurodegenerative Diseases (2 papers), Biochemical and Molecular Research (2 papers) and Pneumocystis jirovecii pneumonia detection and treatment (2 papers). The work is most often cited by research in Clinical Biochemistry (83 citations), Biochemistry (65 citations), Biological Psychiatry (18 citations), Nephrology (45 citations) and Physiology (163 citations). I. Ceballos has collaborated with scholars based in France and Belgium. Frequent co-authors include Annie Nicole, P. Kamoun, P.-M. Sinet, A. Défossez, André Delacourte, Paul Jungers, Pierre‐Marie Sinet, Philippe Chauveau, J Bardet and P Parvy. Their work appears in journals such as Journal of Inherited Metabolic Disease, Kidney International, Clinica Chimica Acta, Advances in experimental medicine and biology and European Journal of Medical 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.

Explore authors with similar magnitude of impact