Stephanie Kleinle
Stephanie Kleinle publishes mostly in Molecular Biology, Genetics and Clinical Biochemistry, on topics such as Mitochondrial Function and Pathology, Metabolism and Genetic Disorders and Genomics and Rare Diseases.
- World rank
- #2,143,787 of 7,710,434 ranked researchers
- Rank in Germany
- #105,760 of 364,343
- Works
- 48
- Citations
- 1.9k
- Citations per work
- 38.6
What does Stephanie Kleinle research?
Stephanie Kleinle's work is mostly in Biochemistry, Genetics and Molecular Biology (67%), Medicine (9%), Neuroscience (8%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences3675.3%
- Everything else715.3%
- Health Sciences59.4%
- Medicine59.4%
- 1Molecular Biology39% of their works
- 2Genetics19% of their works
- 3Clinical Biochemistry9% of their works
- 4Cellular and Molecular Neuroscience8% of their works
- 5Cardiology and Cardiovascular Medicine5% of their works
- 6Pediatrics, Perinatology and Child Health4% of their works
Research topics
- Mitochondrial Function and Pathology
- Metabolism and Genetic Disorders
- Genomics and Rare Diseases
- Genetic Neurodegenerative Diseases
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Which keywords describe Stephanie Kleinle's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Mitochondria, Reactive Oxygen Species, Biochemical Genetics, Metabolic Disorders, Genetic Variants, Sequence Interpretation and Huntington's Disease.
- Sex Determination
- Genomic Imprinting
- RNA methylation
- ATP Synthase
- Huntington's Disease
- Genetic Variants
- Biochemical Genetics
- Mitochondria
- Mitochondrial Dysfunction
- Reactive Oxygen Species
- Metabolic Disorders
- Sequence Interpretation
- Protein Aggregation
- Vacuolar ATPases
- m6A-seq
- Parental Influence
- X Chromosome Inactivation
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most.
All 17 words, with their numbers
- Mitochondrial Dysfunction312 topics
- Mitochondria231 topic
- Reactive Oxygen Species231 topic
- Biochemical Genetics131 topic
- Metabolic Disorders131 topic
- Genetic Variants111 topic
- Sequence Interpretation111 topic
- Huntington's Disease81 topic
- Protein Aggregation81 topic
- ATP Synthase71 topic
- Vacuolar ATPases71 topic
- RNA methylation51 topic
- m6A-seq51 topic
- Genomic Imprinting41 topic
- Parental Influence41 topic
- Sex Determination31 topic
- X Chromosome Inactivation31 topic
Where does Stephanie Kleinle work?
Stephanie Kleinle's main affiliation in the publication record is Medical Genetics Center, Germany.
How many publications and citations does Stephanie Kleinle have?
OpenAlex counts 48 works and 1,851 citations for Stephanie Kleinle, an h-index of 21, ranking #2,143,787 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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