C. Jakobs

10.2k citations

218 papers · 7.1k indexed · h-index 42

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders 147
Biochemistry top 0.2%
- Amino Acid Enzymes and Metabolism 38
Rheumatology top 0.5%
- Folate and B Vitamins Research 34
Obstetrics and Gynecology top 1%
Pediatrics, Perinatology and Child Health top 1%
Molecular Biology
- Peroxisome Proliferator-Activated Receptors 42
- Biochemical and Molecular Research 24
- Mitochondrial Function and Pathology 20
- Metabolomics and Mass Spectrometry Studies 17
Physiology
- Diet and metabolism studies 25

Co-authors: K. Michael Gibson Eduard A. Struys H.J. ten Brink Nanda M. Verhoeven Henk J. Blom Mirjam M. C. Wamelink Johanna I.P. de Vries Gajja S. Salomons
Cited by: Clinical Biochemistry Biochemistry Rheumatology
Journals: Journal of Inherited Metabolic Disease (96 papers)European Journal of Pediatrics (17 papers)Molecular Genetics and Metabolism (9 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

C. Jakobs

217 papers receiving 6.9k citations

Peers

Countries citing papers authored by C. Jakobs

Since Specialization

Citations

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

Fields of papers citing papers by C. Jakobs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Presynapses contain distinct actin nanostructures The Journal of Cell Biology ·S. S. Chen,C. Jakobs,Saad Ajaj,Young Ja Park,Nicolas Jullien,博土屋,G de Araujo Germana,عبد السلام بن صالح الجار الله,Changhyup,Ghislaine Caillol,Yuki Ogawa,Marie‐Jeanne Papandréou,Christophe Leterrier	2023	19
2	Guanidinoacetate methyltransferase deficiency: First steps to newborn screening for a treatable neurometabolic disease Molecular Genetics and Metabolism ·Saadet Mercimek‐Mahmutoglu,Graham Sinclair,Silvy J.M. van Dooren,Warsha A. Kanhai,H. Frohnhäuser,Odette Michel,Stephen Arthur Grill,Титлянова-Чайкина Наталья Викторовна,L. Sweetman,C. Jakobs,Gajja S. Salomons	2012	21
3	A lymphoblast model for IDH2 gain-of-function activity in d-2-hydroxyglutaric aciduria type II: Novel avenues for biochemical and therapeutic studies Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Martijn Kranendijk,Gajja S. Salomons,K. Michael Gibson,Emile Van Schaftingen,C. Jakobs,Eduard A. Struys	2011	12
4	The screening of SLC6A8 deficiency among Estonian families with X‐linked mental retardation Journal of Inherited Metabolic Disease ·姚诗海,Kerstin Käll,Gajja S. Salomons,Inga Talvik,Mairi Männamaa,Reet Rein,C. Jakobs,Katrin Õunap	2009	39
5	Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency Human Genomics ·Patrizia Malaspina,Matthew J. Picklo,C. Jakobs,O. Carter Snead,K. Michael Gibson	2009	27
6	Lipid abnormalities in succinate semialdehyde dehydrogenase (Aldh5a1−/−) deficient mouse brain provide additional evidence for myelin alterations Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Gwendolyn Barceló‐Coblijn,Eric J. Murphy,Kevin Mills,Bryan Winchester,C. Jakobs,O. Carter Snead,K. Michael Gibson	2007	14
7	Overexpression of GAMT restores GAMT activity in primary GAMT-deficient fibroblasts Molecular Genetics and Metabolism ·Lígia S. Almeida,Efraim H. Rosenberg,田淵崇文,Nanda M. Verhoeven,Laura Vilarinho,C. Jakobs,Gajja S. Salomons	2006	6
8	Diagnóstico pré-natal de Síndrome de Smith-Lemli-Opitz Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) ·Maria Luı́s Cardoso,Резникова Оксана Бениаминовна,Sérgio Castedo,Carmen Depasquale,Nuno Montenegro,C. Jakobs,Peter T. Clayton,Laura Vilarinho	2005	0
9	L-2-hydroxyglutaric aciduria: novel mutations in the L-2-hydroxyglutarate dehydrogenase gene Journal of Inherited Metabolic Disease ·まなびあテラス,Shu min He,Nelida Jeanette Sánchez Ramos,Nasrin Mohassel Akhlaghi,Antònia Ribes,G. R. Voots,Tran Quoc Toan,Bernd A. Neubauer,Stanley H. Korman,Till Rümenapf,Yeswanth Akula,Hui-qin Tao,S H Seyedi,Vishnu Hegde,Christine Vianey‐Saban,Dimitrios Zafeiriou,Mohnish Suri,Reschi Dwi Fitri,S H Cook,C. Jakobs	2005	1
10	Molecular studies in Portuguese patients with Smith–Lemli–Opitz syndrome and report of three new mutations in DHCR7 Molecular Genetics and Metabolism ·Maria Luı́s Cardoso,Jaime Mauricio Torrez Rivera,Esmeralda Martins,Luís Nunes,Imataka Kiyoharu,Luyang Yu,مهرانوش امامیان طبرستانی,Aubrey Hounshell,Ana Medeira,Romina Pérez Manelli,Sónia N. Pedro,Ž. Plantić,Carlo Dionisi‐Vici,Filippo M. Santorelli,C. Jakobs,Peter T. Clayton,Laura Vilarinho	2005	8
11	[6S]5-methyltetrahydrofolate or folic acid supplementation and absorption and initial elimination of folate in young and middle-aged adults European Journal of Clinical Nutrition ·K. de Meer,Yvo M. Smulders,J. Dainty,Desirée E.C. Smith,Rob Kok,Coen D.A. Stehouwer,Paul Finglas,C. Jakobs	2005	23
12	The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family Molecular Genetics and Metabolism ·Soumeya Bekri,Punky Kusuma Damayanti,道一井芹,東京消防庁消防科学研究所第研究室,Gajja S. Salomons,C. Jakobs,E Van Obberghen	2004	13
13	S‐adenosylhomocysteine and the ratio of S‐adenosylmethionine to S‐adenosylhomocysteine are not related to folate, cobalamin and vitamin B6 concentrations European Journal of Clinical Investigation ·(unknown),Yvo M. Smulders,Tom Teerlink,Eduard A. Struys,K. de Meer,Piet J. Kostense,C. Jakobs,Joost Dekker,Giel Nijpels,Robert J. Heine,L.M. Bouter,Coen D.A. Stehouwer	2003	39
14	Plasma homocysteine and S-adenosylmethionine in erythrocytes as determinants of carotid intima-media thickness: different effects in diabetic and non-diabetic individuals Atherosclerosis ·(unknown),Ronald M.A. Henry,Piet J. Kostense,C. Jakobs,Tom Teerlink,Sonja Zweegman,Joost Dekker,Giel Nijpels,Robert J. Heine,L.M. Bouter,Yvo M. Smulders,Coen D.A. Stehouwer	2003	32
15	Determination of isotopic enrichments of [1-13C]homocysteine, [1-13C]methionine and [2H3-methyl-1-13C]methionine in human plasma by gas chromatography–negative chemical ionization mass spectrometry Journal of Chromatography B Biomedical Sciences and Applications ·Wim Kulik,Rob Kok,K. de Meer,C. Jakobs	2000	8
16	Hyperhomocysteinaemia is not related to risk of distal somatic polyneuropathy: The Hoorn Study Journal of Internal Medicine ·Ellen K. Hoogeveen,Piet J. Kostense,Gerlof D. Valk,Frits W. Bertelsmann,C. Jakobs,Joost Dekker,Giel Nijpels,Robert J. Heine,L.M. Bouter,Coen D.A. Stehouwer	1999	16
17	L-2-Hydroxyglutaric Aciduria: Clinical Heterogeneity Versus Biochemical Homogeneity in a Sibship Neuropediatrics ·So In Yung,J. G. M. Huijmans,Hans Stroink,Simon G. F. Robben,C. Jakobs,M. Durán	1997	18
18	Phytanoyl-CoA Hydroxylase Is Present in Human Liver, Located in Peroxisomes, and Deficient in Zellweger Syndrome: Direct, Unequivocal Evidence for the New, Revised Pathway of Phytanic Acid α-Oxidation in Humans Biochemical and Biophysical Research Communications ·Gerbert A. Jansen,Stephanie J. Mihalik,Paul A. Watkins,H. W. Moser,C. Jakobs,Simone Denis,R. J. A. Wanders	1996	70
19	Galactitol in galactosemia European Journal of Pediatrics ·C. Jakobs,S. Schweitzer,Bert Dorland	1995	36
20	Prenatal diagnosis of isovaleric acidaemia by enzyme and metabolite assay in the first and second trimesters Prenatal Diagnosis ·Wim J. Kleijer,Luo Qiyang,J. G. M. Huijmans,itwriter,C. Jakobs	1995	5

About C. Jakobs

C. Jakobs is a scholar working on Clinical Biochemistry, Biochemistry and Rheumatology, having authored 218 papers that have together received 7.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (147 papers), Peroxisome Proliferator-Activated Receptors (42 papers), Amino Acid Enzymes and Metabolism (38 papers), Folate and B Vitamins Research (34 papers), Diet and metabolism studies (25 papers), Biochemical and Molecular Research (24 papers), Mitochondrial Function and Pathology (20 papers) and Metabolomics and Mass Spectrometry Studies (17 papers). The work is most often cited by research in Clinical Biochemistry (2.8k citations), Biochemistry (896 citations) and Rheumatology (1.5k citations). C. Jakobs has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include K. Michael Gibson, Eduard A. Struys, H.J. ten Brink, Nanda M. Verhoeven, Henk J. Blom, Mirjam M. C. Wamelink, Johanna I.P. de Vries, Gajja S. Salomons, G.A. Dekker and B. Mary E. von Blomberg. Their work appears in journals such as Journal of Inherited Metabolic Disease, European Journal of Pediatrics, Molecular Genetics and Metabolism, Neuropediatrics and Journal of Lipid Research.

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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