Talaat I. Farag
Talaat I. Farag publishes mostly in Genetics, Molecular Biology and Surgery, on topics such as Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics and Connective tissue disorders research.
- World rank
- #5,660,895 of 7,710,434 ranked researchers
- Rank in Kuwait
- #1,695 of 2,469
- Works
- 94
- Citations
- 1.7k
- Citations per work
- 17.9
What does Talaat I. Farag research?
Talaat I. Farag's work is mostly in Biochemistry, Genetics and Molecular Biology (42%), Medicine (26%).
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 Sciences3941.5%
- Everything else3032.0%
- Health Sciences2526.5%
- Medicine2526.5%
- 1Genetics29% of their works
- 2Molecular Biology13% of their works
- 3Surgery10% of their works
- 4Pediatrics, Perinatology and Child Health10% of their works
- 5Genetics4% of their works
- 6Rheumatology3% of their works
Research topics
- Genomic variations and chromosomal abnormalities
- Prenatal Screening and Diagnostics
- Connective tissue disorders research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Sexual Differentiation and Disorders
- Metabolism and Genetic Disorders
- Congenital limb and hand anomalies
Which keywords describe Talaat I. Farag's research?
The keywords of their largest research topics: Copy Number Variation, Genomic Rearrangements, Aneuploidy Screening, Prenatal Diagnosis, Congenital Adrenal Hyperplasia, Ehlers-Danlos Syndrome, Genomic Imprinting and Marfan Syndrome.
- Metabolic Disorders
- Genetic Heterogeneity
- X Chromosome Inactivation
- Sex Determination
- Marfan Syndrome
- Ehlers-Danlos Syndrome
- Prenatal Diagnosis
- Genomic Rearrangements
- Copy Number Variation
- Aneuploidy Screening
- Congenital Adrenal Hyperplasia
- Genomic Imprinting
- Parental Influence
- Steroid 21-Hydroxylase Deficiency
- Biochemical Genetics
- Limb Malformations
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 16 words, with their numbers
- Copy Number Variation191 topic
- Genomic Rearrangements191 topic
- Aneuploidy Screening161 topic
- Prenatal Diagnosis161 topic
- Congenital Adrenal Hyperplasia91 topic
- Ehlers-Danlos Syndrome91 topic
- Genomic Imprinting91 topic
- Marfan Syndrome91 topic
- Parental Influence91 topic
- Sex Determination91 topic
- Steroid 21-Hydroxylase Deficiency91 topic
- X Chromosome Inactivation91 topic
- Biochemical Genetics71 topic
- Genetic Heterogeneity71 topic
- Limb Malformations71 topic
- Metabolic Disorders71 topic
Where does Talaat I. Farag work?
Talaat I. Farag's main affiliation in the publication record is Kuwait Institute for Medical Specialization, Kuwait.
How many publications and citations does Talaat I. Farag have?
OpenAlex counts 94 works and 1,680 citations for Talaat I. Farag, an h-index of 20, ranking #5,660,895 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.
Discussion
Ask a question or share a note about Talaat I. Farag. Keep it to the research: no personal attacks, advertising or links. Any reader can report a post, which collapses it for everyone until it is opened.