₂₈Ronald J A Wanders

Summary for 2004 [at-glance overview of Ronald J A Wanders work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Ronald J A Wanders. According to available data, in 2004 Ronald J A Wanders published at least 28 articles. This work was completed in collaboration with several authors including Waterham, Hans R and Duran, Marinus. Many other authors have collaborated with Ronald J A Wanders as well. There is no information about the funding or the grants awarded to support this work.

Ronald J A Wanders is a key opinion leader in numerous areas including Fibroblasts, Peroxisomes, Peroxisomal Disorders, Cytosol, Genetic Complementation Test. This author's highest rank is 1 when compared to all other authors using the keyword Peroxisomes. Analysis of the article abstracts and the titles suggests that Ronald J A Wanders professional interests are focused around "peroxisome biogenesis disorders", "role peroxisomes isoprenoid" and "peroxisome biogenesis disorder". These might also be referred to as "peroxisome biogenesis", "barth syndrome" or "refsum disease". Statistical analysis shows that Ronald J A Wanders's writing is likely to contains terms "patients", "peroxisomal", "gene", "human", "mutations" and "acid".

Unfortunately, there is not enough information to establish Ronald J A Wanders affiliation. Luckily, several email addresses are on file.

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Alternative names (1) [other authors with names similar to Ronald J A Wanders]

₆₉Wanders, R J A

Year 2004 Charts [Ronald J A Wanders frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Ronald J A Wanders publication and funding history for the range of years]

Emails (11) [email addresses extracted from Ronald J A Wanders affiliations]

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Ronald J A Wanders Coauthors (70) [all coauthors with the number of joint publications]

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₂Ferdinandusse, Sacha

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₂Jansen, Gerbert A

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₂Ruiter, Jos P N

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₂van Roermund, Carlo W T

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₈Zafeiriou, Dimitrios I

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₆Majoie, Charles B L M

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₆Osumi, Takashi

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₅Burgering, Boudewijn M T

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₃Rontani, Jean-François

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₂Prud'homme, Jean-François

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₂Trefz, Friedrich K

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₂Wijburg, Frits A

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₂van Marle, Jan

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₂van Spronsen, Francjan J

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₁Admiraal, Ronald J C

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₁de Almeida, Isabel Tavares

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₁van Woerden, Christiaan S

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₁van den Brink, Daan M

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Affiliations (27) [condensed summary of the Ronald J A Wanders affiliations, the leading number and the color conveys importance]

₂Department of Clinical Chemistry, Academic Medical Center, University of Amsterdam, The Netherlands.
₁Department of General Neurology, Hertie Institute for Clinical Brain Research, Tübingen, Germany.
₁Department of Clinical Chemistry and Pediatrics, University of Amsterdam, The Netherlands.
₁Department of Pediatrics, Child Neurology, Hacettepe University Medical Faculty, Ankara, Turkey.
₁University of Amsterdam, Academic Medical Center, Department of Pediatrics/Emma Children's Hospital, Laboratory for Genetic Metabolic Diseases, The Netherlands.
₁Department of Biological Sciences, Wayne State University, Detroit, Michigan 48202, USA.
₁Academic Medical Centre, Departments of Clinical Chemistry and Pediatrics, Emma Children's Hospital, University of Amsterdam, Amsterdam, The Netherlands.
₁Institute of Child Health, Athens, Greece.
₁Department of Clinical Chemistry, University of Amsterdam, Academic Medical Centre, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
₁Emma Children's Hospital AMC, Amsterdam, The Netherlands.
₁Department of General Pediatrics, University Children's Hospital, Moorenstrasse 5, D-40225, Düsseldorf, Germany.
₁Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan.
₁Departments of Clinical Chemistry, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
₁University of Amsterdam, Academic Medical Centre, Department of Clinical Chemistry, Emma Children's Hospital, Laboratory of Genetic Metabolic Diseases, Amsterdam, The Netherlands.
₁Department of Pediatric Neurology, Emma Children's Hospital/AMC, University of Amsterdam, Amsterdam, The Netherlands.
₁Department of Pediatrics, Emma Children's Hospital, Amsterdam, The Netherlands.
₁Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center of Groningen, Groningen, The Netherlands.
₁Department of Clinical Chemistry, University of Amsterdam, Academic Medical Center, Emma Children's Hospital, The Netherlands.
₁Laboratory Genetic Metabolic Diseases, Department of Clinical Chemistry, Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
₁Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
₁Lab. Genetic Metabolic Diseases (F0-224), Department of Clinical Chemistry and Peadiatrics, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
₁Laboratory of Genetic Metabolic Diseases, Department of Clinical Chemistry, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
₁Laboratory of Genetic Metabolic Diseases, Departments of Clinical Chemistry and Pediatrics/Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
₁Department of Clinical Chemistry, Academic Medical Center, Lab Genetic Metabolic Diseases, F0-224, Meibergdreef 9, Amsterdam 1105 AZ, Netherlands.
₁Laboratory Genetic Metabolic Diseases, Department of Pediatrics, Emma Children's Hospital, Academic Medical Center, Amsterdam.
₁Department of Biological Science, Wayne State University, Detroit, MI 48202, USA.
₁Department of Biochemistry of Lipids, Institute of Biomembranes, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.

Key Opinion Leader In [Ronald J A Wanders is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

₁Peroxisomes | ₁Peroxisomal Disorders | ₂Consanguinity | ₂Genetic Complementation Test | ₂Cardiolipins | ₂Fibroblasts | ₃Cytosol | ₁₀Oxidation-Reduction | ₁₄Membrane Proteins | ₂₂Mutation | ₃₃Phenotype | ₃₆Skin | ₄₄Fatty Acids | ₆₄Lipid Peroxidation | ₆₈DNA Primers | ₉₇Cells, Cultured | ₁₄₆Kidney | ₁₅₄Carrier Proteins | ₁₇₀Liver | ₁₈₄Saccharomyces cerevisiae | ₂₃₇Transcription Factors | ₂₅₆Base Sequence | ₄₄₁Humans | ₄₆₅Child, Preschool | ₅₆₁Cell Line | ₅₉₈Magnetic Resonance Imaging

Keywords (32) [keywords assigned to Ronald J A Wanders articles by PubMed, the leading number and the color conveys importance]

₂₆Humans | ₁₀Fibroblasts | ₉Mutation | ₈Peroxisomes | ₇Membrane Proteins | ₇Female | ₆Peroxisomal Disorders | ₆Cells, Cultured | ₆Oxidation-Reduction | ₆Male | ₅Cytosol | ₅Genetic Complementation Test | ₄Base Sequence | ₄Adolescent | ₄Transcription Factors | ₄Skin | ₄Fatty Acids | ₄Child, Preschool | ₄Magnetic Resonance Imaging | ₄Adult | ₄Liver | ₄Phenotype | ₃Consanguinity | ₃Carrier Proteins | ₃Child | ₃Kidney | ₃Animals | ₃Lipid Peroxidation | ₃Cell Line | ₃Saccharomyces cerevisiae | ₃Cardiolipins | ₃DNA Primers

Ronald J A Wanders Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Ronald J A Wanders might be a good expert witness on these terms]

₄₁patients | ₂₈peroxisomal | ₂₆gene | ₂₆human | ₂₃mutations | ₂₂acid | ₂₀disease | ₂₀deficiency | ₁₉protein | ₁₉disorders | ₁₈cells | ₁₇fibroblasts | ₁₆syndrome | ₁₆mutation | ₁₅biogenesis | ₁₅mutant | ₁₅fatty | ₁₄peroxisome | ₁₄beta-oxidation | ₁₃identification | ₁₃metabolism | ₁₂barth | ₁₂cl | ₁₂involved | ₁₂peroxisomes | ₁₂group | ₁₁taz1delta | ₁₁patient | ₁₁found | ₁₁role | ₁₀mitochondrial | ₁₀enzymes
₁₄peroxisome biogenesis | ₁₂barth syndrome | ₉refsum disease | ₈biogenesis disorders | ₇taz1delta mutant | ₆fatty acid | ₆enzymes involved | ₆molecular basis | ₅isoprenoid biosynthesis | ₅peroxisomes isoprenoid | ₅phosphomevalonate kinase | ₅fatty acids | ₅role peroxisomes | ₄pex12 gene | ₄patients peroxisomal | ₄kinase cytosolic | ₄skin fibroblasts | ₄patients homozygous | ₃gly170arg phe152ile | ₃pex2 gene | ₃basis refsum | ₃biosynthetic pathway | ₃mutations pex2 | ₃chromosome 14q22 | ₃localized chromosome | ₃clinical implications | ₃c14orf160 localized | ₃indication peroxisomal | ₃yeast taz1delta | ₃clinical outcome | ₃gene c14orf160 | ₃mutations pex12
₈peroxisome biogenesis disorders | ₅role peroxisomes isoprenoid | ₅peroxisome biogenesis disorder | ₅patients peroxisome biogenesis | ₅mevalonate pyrophosphate decarboxylase | ₄peroxisomes isoprenoid biosynthesis | ₄pbd patients belonging | ₄human mevalonate pyrophosphate | ₄sterol carrier protein | ₃mutations pex12 gene | ₃localized chromosome 14q22 | ₃mutations pex2 gene | ₃molecular basis refsum | ₃c14orf160 localized chromosome | ₃gene c14orf160 localized | ₃yeast taz1delta mutant | ₃basis refsum disease | ₃presenting leber congenital | ₃without overt cardiomyopathy | ₃neutropenia barth syndrome | ₃phytol phytanic acid | ₃human phosphomevalonate kinase | ₃cardioskeletal myopathy neutropenia | ₃deficiency presenting leber | ₃inborn errors metabolism | ₃breakdown phytol phytanic | ₃results support central | ₃primary hyperoxaluria type | ₃leber congenital amaurosis | ₃support central role | ₃conventional subcellular fractionation | ₃ventricular fibrillation without

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