Bochra Ben Rhouma
Bochra Ben Rhouma publishes mostly in Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism, on topics such as Sexual Differentiation and Disorders, Hormonal and reproductive studies and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities.
- World rank
- #5,175,681 of 7,710,434 ranked researchers
- Rank in Tunisia
- #4,939 of 12,803
- Works
- 26
- Citations
- 279
- Citations per work
- 10.7
What does Bochra Ben Rhouma research?
Bochra Ben Rhouma's work is mostly in Biochemistry, Genetics and Molecular Biology (47%), Medicine (23%), Neuroscience (3%).
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 Sciences1350.0%
- Everything else727.4%
- Health Sciences622.6%
- Medicine622.6%
- 1Molecular Biology30% of their works
- 2Genetics17% of their works
- 3Endocrinology, Diabetes and Metabolism14% of their works
- 4Hematology4% of their works
- 5Rheumatology4% of their works
- 6Developmental Neuroscience3% of their works
Research topics
- Sexual Differentiation and Disorders
- Hormonal and reproductive studies
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hormonal Regulation and Hypertension
- Metabolism and Genetic Disorders
- Diabetes and associated disorders
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Which keywords describe Bochra Ben Rhouma's research?
The keywords of their largest research topics: Genetic Variants, Congenital Adrenal Hyperplasia, Steroid 21-Hydroxylase Deficiency, Metabolic Syndrome, Hormone Therapy, Testosterone, Aldosterone and Primary Aldosteronism.
- Type 1 Diabetes
- Rett Syndrome
- Genetics
- Clinical Genomics
- X Chromosome Inactivation
- Primary Aldosteronism
- Testosterone
- Metabolic Syndrome
- Congenital Adrenal Hyperplasia
- Genetic Variants
- Steroid 21-Hydroxylase Deficiency
- Hormone Therapy
- Aldosterone
- Sex Determination
- Biochemical Genetics
- Fragile X Syndrome
- Metabolic Disorders
- Sequence Interpretation
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. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.
All 18 words, with their numbers
- Genetic Variants112 topics
- Congenital Adrenal Hyperplasia91 topic
- Steroid 21-Hydroxylase Deficiency91 topic
- Metabolic Syndrome82 topics
- Hormone Therapy51 topic
- Testosterone51 topic
- Aldosterone31 topic
- Primary Aldosteronism31 topic
- Sex Determination31 topic
- X Chromosome Inactivation31 topic
- Biochemical Genetics21 topic
- Clinical Genomics21 topic
- Fragile X Syndrome21 topic
- Genetics21 topic
- Metabolic Disorders21 topic
- Rett Syndrome21 topic
- Sequence Interpretation21 topic
- Type 1 Diabetes21 topic
Where does Bochra Ben Rhouma work?
Bochra Ben Rhouma's main affiliation in the publication record is Hopital Universitaire Hedi Chaker, Tunisia.
How many publications and citations does Bochra Ben Rhouma have?
OpenAlex counts 26 works and 279 citations for Bochra Ben Rhouma, an h-index of 10, ranking #5,175,681 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised citation 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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