M. Y. El‐Khalifa
M. Y. El‐Khalifa publishes mostly in Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, on topics such as Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases and Sexual Differentiation and Disorders.
- World rank
- #4,060,071 of 7,710,434 ranked researchers
- Rank in Kuwait
- #1,135 of 2,469
- Works
- 18
- Citations
- 511
- Citations per work
- 28.4
What does M. Y. El‐Khalifa research?
M. Y. El‐Khalifa's work is mostly in Biochemistry, Genetics and Molecular Biology (44%), Medicine (23%), Immunology and Microbiology (4%).
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 Sciences948.0%
- Everything else528.9%
- Health Sciences423.1%
- Medicine423.1%
- 1Genetics33% of their works
- 2Molecular Biology12% of their works
- 3Pediatrics, Perinatology and Child Health10% of their works
- 4Surgery8% of their works
- 5Genetics6% of their works
- 6Immunology4% of their works
Research topics
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Sexual Differentiation and Disorders
- Prenatal Screening and Diagnostics
- Forensic and Genetic Research
- Connective tissue disorders research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Which keywords describe M. Y. El‐Khalifa's research?
The keywords of their largest research topics: Genetic Variants, Copy Number Variation, Genomic Rearrangements, Aneuploidy Screening, Clinical Genomics, Congenital Adrenal Hyperplasia, Prenatal Diagnosis and Sequence Interpretation.
- Sex Determination
- Marfan Syndrome
- Fragile X Syndrome
- Ancient DNA
- Sequence Interpretation
- Congenital Adrenal Hyperplasia
- Aneuploidy Screening
- Copy Number Variation
- Genetic Variants
- Genomic Rearrangements
- Clinical Genomics
- Prenatal Diagnosis
- Steroid 21-Hydroxylase Deficiency
- Ehlers-Danlos Syndrome
- Genomic Analysis
- Rett Syndrome
- 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. 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 17 words, with their numbers
- Genetic Variants62 topics
- Copy Number Variation41 topic
- Genomic Rearrangements41 topic
- Aneuploidy Screening31 topic
- Clinical Genomics31 topic
- Congenital Adrenal Hyperplasia31 topic
- Prenatal Diagnosis31 topic
- Sequence Interpretation31 topic
- Steroid 21-Hydroxylase Deficiency31 topic
- Ancient DNA21 topic
- Ehlers-Danlos Syndrome21 topic
- Fragile X Syndrome21 topic
- Genomic Analysis21 topic
- Marfan Syndrome21 topic
- Rett Syndrome21 topic
- Sex Determination21 topic
- X Chromosome Inactivation21 topic
Where does M. Y. El‐Khalifa work?
M. Y. El‐Khalifa's main affiliation in the publication record is Kuwait Institute for Medical Specialization, Kuwait.
How many publications and citations does M. Y. El‐Khalifa have?
OpenAlex counts 18 works and 511 citations for M. Y. El‐Khalifa, an h-index of 9, ranking #4,060,071 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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