Matthew H. McIntyre
Matthew H. McIntyre publishes mostly in Genetics, Molecular Biology and Experimental and Cognitive Psychology, on topics such as Genetic Associations and Epidemiology, Parkinson's Disease Mechanisms and Treatments and Sexual Differentiation and Disorders.
- World rank
- #14,507 of 7,710,434 ranked researchers
- Rank in United States
- #5,117 of 1,627,098
- Works
- 139
- Citations
- 14k
- Citations per work
- 100.7
What does Matthew H. McIntyre research?
Matthew H. McIntyre's work is mostly in Biochemistry, Genetics and Molecular Biology (31%), Medicine (7%), Psychology (6%).
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
- Everything else7352.5%
- Life Sciences4834.6%
- Health Sciences107.4%
- Medicine107.4%
- Social Sciences85.5%
- Psychology85.5%
- 1Genetics22% of their works
- 2Molecular Biology9% of their works
- 3Experimental and Cognitive Psychology6% of their works
- 4Neurology4% of their works
- 5Epidemiology3% of their works
- 6Cognitive Neuroscience3% of their works
Research topics
- Genetic Associations and Epidemiology
- Parkinson's Disease Mechanisms and Treatments
- Sexual Differentiation and Disorders
- Evolutionary Psychology and Human Behavior
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Which keywords describe Matthew H. McIntyre's research?
The keywords of their largest research topics: Genetic Variation, Genome-Wide Association, a-Synuclein, Parkinson's Disease, Congenital Adrenal Hyperplasia, Evolutionary Psychology, Human Behavior and Steroid 21-Hydroxylase Deficiency.
- X Chromosome Inactivation
- Genomic Rearrangements
- BRCA2
- Rett Syndrome
- Steroid 21-Hydroxylase Deficiency
- Evolutionary Psychology
- a-Synuclein
- Genome-Wide Association
- Genetic Variation
- Parkinson's Disease
- Congenital Adrenal Hyperplasia
- Human Behavior
- Fragile X Syndrome
- BRCA1
- Copy Number Variation
- Sex Determination
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
- Genetic Variation361 topic
- Genome-Wide Association361 topic
- Parkinson's Disease111 topic
- a-Synuclein111 topic
- Congenital Adrenal Hyperplasia101 topic
- Evolutionary Psychology101 topic
- Human Behavior101 topic
- Steroid 21-Hydroxylase Deficiency101 topic
- Fragile X Syndrome71 topic
- Rett Syndrome71 topic
- BRCA161 topic
- BRCA261 topic
- Copy Number Variation61 topic
- Genomic Rearrangements61 topic
- Sex Determination51 topic
- X Chromosome Inactivation51 topic
Where does Matthew H. McIntyre work?
Matthew H. McIntyre's main affiliation in the publication record is 23andMe (United States), United States.
How many publications and citations does Matthew H. McIntyre have?
OpenAlex counts 139 works and 13,995 citations for Matthew H. McIntyre, an h-index of 51, ranking #14,507 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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