Mike Gerards

1.7k citations

33 papers · 910 · h-index 18

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Aging top 10%

Papers in

Molecular Biology 32
- Mitochondrial Function and Pathology 31
- ATP Synthase and ATPases Research 12
- Genomics and Phylogenetic Studies 2
- Metabolomics and Mass Spectrometry Studies 2
- RNA modifications and cancer 2
Clinical Biochemistry 12
- Metabolism and Genetic Disorders 12

Co-authors: Hubert J.M. Smeets (20 shared papers)I.F.M. de Coo (16 shared papers)Suzanne C.E.H. Sallevelt (4 shared papers)B.J.C. van den Bosch (5 shared papers)Rick Kamps (7 shared papers)H.R. Scholte (4 shared papers)Debby M.E.I. Hellebrekers (8 shared papers)Kees Schoonderwoerd (5 shared papers)
Journals: Mitochondrion (6 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Brain (2 papers)Biomolecules (2 papers)
Partner nations: Netherlands Finland Belgium

In The Last Decade

Mike Gerards

33 papers receiving 901 citations

Peers

Countries citing papers authored by Mike Gerards

Since Specialization

Citations

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

Fields of papers citing papers by Mike Gerards

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options Molecular Genetics and Metabolism ·Mike Gerards, Suzanne C.E.H. Sallevelt, Hubert J.M. Smeets	2015	89
2	Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene Brain ·Mike Gerards, B.J.C. van den Bosch, Katharina Danhauser, Valérie Serre, Michel van Weeghel, Ronald J. A. Wanders, Gerry A. F. Nicolaes, Wim J. Sluiter, Kees Schoonderwoerd, H.R. Scholte, Holger Prokisch, Agnès Rötig, I.F.M. de Coo, Hubert J.M. Smeets	2010	86
3	Exome sequencing reveals a novel Moroccan founder mutation inSLC19A3as a new cause of early-childhood fatal Leigh syndrome Brain ·Mike Gerards, Rick Kamps, Jo van Oevelen, Iris Boesten, Eveline Jongen, Bart de Koning, H.R. Scholte, Isabel de Angst, Kees Schoonderwoerd, Abdelaziz Sefiani, Ilham Ratbi, Wouter Coppieters, Latifa Karim, I.F.M. de Coo, Bianca van den Bosch, Hubert J.M. Smeets	2013	69
4	Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause Frontiers in Genetics ·Tom E. J. Theunissen, Minh Nguyen, Rick Kamps, Alexandra T.M. Hendrickx, Suzanne C.E.H. Sallevelt, Ralph W.H. Gottschalk, Chantal Calis, Alphons P. M. Stassen, Bart de Koning, Elvira N. M. Mulder-Den Hartog, Kees Schoonderwoerd, Sabine A. Fuchs, Yvonne Hilhorst‐Hofstee, Marjolein Visser, Jo Vanoevelen, Radek Szklarczyk, Mike Gerards, I.F.M. de Coo, Debby M.E.I. Hellebrekers, Hubert J.M. Smeets	2018	62
5	Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome Journal of Medical Genetics ·Mike Gerards, Wim J. Sluiter, B.J.C. van den Bosch, L. Elly A. de Wit, Chantal Calis, M. Frentzen, Hana Akbari, Kees Schoonderwoerd, H.R. Scholte, R. J. E. Jongbloed, Alexandra T.M. Hendrickx, I.F.M. de Coo, Hubert J.M. Smeets	2009	59
6	Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy Mitochondrion ·Mike Gerards, Bianca van den Bosch, Chantal Calis, Kees Schoonderwoerd, Klaartje van Engelen, Marina A.J. Tijssen, I.F.M. de Coo, Anneke J. van der Kooi, Hubert J.M. Smeets	2010	55
7	Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors Annals of Neurology ·Juan Darío Ortigoza‐Escobar, Majid Alfadhel, Marta Molero-Luís, Niklas Darín, Ronen Spiegel, I.F.M. de Coo, Mike Gerards, Robert W. Taylor, Rafael Artuch, Marwan Nashabat, Pilar Rodríguez‐Pombo, Brahim Tabarki, Belén Pérez‐Dueñas, (unknown)	2017	48
8	Defective NDUFA9 as a novel cause of neonatally fatal complex I disease Journal of Medical Genetics ·B.J.C. van den Bosch, Mike Gerards, Wim J. Sluiter, Alexander P.A. Stegmann, Eveline Jongen, Debby M.E.I. Hellebrekers, Renske Oegema, Ellen Lambrichs, Holger Prokisch, Katharina Danhauser, Kees Schoonderwoerd, I.F.M. de Coo, Hubert J.M. Smeets	2011	46
9	Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline Cells Cell Reports ·Auke B.C. Otten, Tom E. J. Theunissen, Josien G. Derhaag, Ellen Lambrichs, Iris Boesten, Marie Winandy, Aafke P.A. van Montfoort, Katsiaryna Tarbashevich, Erez Raz, Mike Gerards, Jo Vanoevelen, B.J.C. van den Bosch, Marc Müller, Hubert J.M. Smeets	2016	41
10	A hitchhiker’s guide to mitochondrial quantification Mitochondrion ·Irene M. G. M. Hemel, Bob P. H. Engelen, Nicole Luber, Mike Gerards	2021	38
11	Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthase Molecular Systems Biology ·Atsushi Fukuoh, Giuseppe Cannino, Mike Gerards, Suzanne M. K. Buckley, Selena Kazancioglu, Filippo Scialò, Eero Lihavainen, André S. Ribeiro, Éric Dufour, Howard T. Jacobs	2014	36
12	mtDNA point mutations are present at various levels of heteroplasmy in human oocytes Molecular Human Reproduction ·L.J.A.M. Jacobs, Mike Gerards, Patrick F. Chinnery, John C.M. Dumoulin, I.F.M. de Coo, Joep Geraedts, Hubert J.M. Smeets	2007	34
13	Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos Frontiers in Cell and Developmental Biology ·Auke B.C. Otten, Rick Kamps, Patrick Lindsey, Mike Gerards, Hélène Pendeville-Samain, Marc Müller, Florence H. J. van Tienen, H.J.M. Smeets	2020	32
14	Novel pathogenic SLC25A46 splice‐site mutation causes an optic atrophy spectrum disorder Clinical Genetics ·Minh Nguyen, Iris Boesten, Debby M.E.I. Hellebrekers, N. M. Mulder‐den Hartog, I.F.M. de Coo, Hubert J.M. Smeets, Mike Gerards	2016	30
15	Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients Genetics in Medicine ·Rudy G. E. van Eijsden, Mike Gerards, Lars Eijssen, Alexandra T.M. Hendrickx, Roselie Jongbloed, John H. J. Wokke, Rogier Q. Hintzen, Maria Estela Rubio‐Gozalbo, I.F.M. de Coo, Egill Briem, Valeria Tiranti, Hubert J.M. Smeets	2006	28
16	Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects Frontiers in Neurology ·Tom E. J. Theunissen, Radek Szklarczyk, Mike Gerards, Debby M.E.I. Hellebrekers, Elvira N. M. Mulder-Den Hartog, Jo Vanoevelen, Rick Kamps, Bart de Koning, S. Lane Rutledge, Thomas Schmitt‐Mechelke, Carola G.M. van Berkel, Marjo S. van der Knaap, I.F.M. de Coo, Hubert J.M. Smeets	2016	21
17	Ciona intestinalis NADH dehydrogenase NDX confers stress-resistance and extended lifespan on Drosophila Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Dmytro V. Gospodaryov, Oleh Lushchak, Bohdana M. Rovenko, Natalia V. Perkhulyn, Mike Gerards, Tea Tuomela, Howard T. Jacobs	2014	19
18	Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy European Journal of Human Genetics ·Minh Nguyen, Iris Boesten, Debby M.E.I. Hellebrekers, Jo Vanoevelen, Rick Kamps, Bart de Koning, I.F.M. de Coo, Mike Gerards, Hubert J.M. Smeets	2015	18
19	Elevated mitochondrial DNA copy numbers in pediatric acute lymphoblastic leukemia: A potential biomarker for predicting inferior survival Pediatric Blood & Cancer ·Ayushi Jain, Sameer Bakhshi, Himani Thakkar, Mike Gerards, Archna Singh	2017	14
20	It takes two to tango: The essential role of ER-mitochondrial contact sites in mitochondrial dynamics The International Journal of Biochemistry & Cell Biology ·Irene M. G. M. Hemel, Rita Sarantidou, Mike Gerards	2021	12

About Mike Gerards

Mike Gerards is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Cell Biology and Public Health, Environmental and Occupational Health, having authored 33 papers that have together received 910 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (12 papers), ATP Synthase and ATPases Research (12 papers), Genetic Neurodegenerative Diseases (4 papers), Genomics and Phylogenetic Studies (2 papers), Alcoholism and Thiamine Deficiency (2 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Clinical Biochemistry (402 citations), Aging (28 citations), Molecular Biology (728 citations), Biochemistry (69 citations) and Neurology (77 citations). Mike Gerards has collaborated with scholars based in Netherlands, Finland and Belgium. Frequent co-authors include Hubert J.M. Smeets, I.F.M. de Coo, Suzanne C.E.H. Sallevelt, B.J.C. van den Bosch, Rick Kamps, H.R. Scholte, Debby M.E.I. Hellebrekers, Kees Schoonderwoerd, Wim J. Sluiter and Kees Schoonderwoerd. Their work appears in journals such as Mitochondrion, European Journal of Human Genetics, Journal of Medical Genetics, Brain and Biomolecules.

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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Mike Gerards

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