Benjamin Neale

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Benjamin Neale
EducationUniversity of Chicago
Virginia Commonwealth University (B.Sc., 2006)[1]
King's College London (Ph.D., 2009)[2]
Known forPsychiatric genetics
AwardsLeena Peltonen Prize for Excellence in Human Genetics (2016)
Scientific career
FieldsHuman genetics
Statistical genetics
InstitutionsBroad Institute
Harvard Medical School
Massachusetts General Hospital
Websitewww.nealelab.is

Benjamin Michael Neale is a statistical geneticist with a specialty in psychiatric genetics. He is an institute member at the Broad Institute as well as an associate professor at both Harvard Medical School and the Analytic and Translational Genetics Unit at Massachusetts General Hospital.[3] Neale specializes in genome-wide association studies (GWAS).[3] He was responsible for the data analysis of the first GWAS on attention-deficit/hyperactivity-disorder, and he developed new analysis software such as PLINK,[4] which allows for whole-genome data to be analyzed for specific gene markers. Related to his work on GWAS, Neale is the lead of the ADHD psychiatric genetics and also a member of the Psychiatric GWAS Consortium analysis committee.[citation needed][not verified in body]

Education[edit]

Neale's academic background includes a Genetics Bachelor's of Science degree from the University of Chicago and a Ph.D. in human genetics from King’s College. His postdoctoral project was done in the laboratory of Mark Daly at Massachusetts General Hospital.[5] Neale was recently awarded the 2020 Early-Career Award by the American Society of Human Genetics for his emphasis on using statistical methodology in his research analyses.[6]

Research[edit]

Neale has published work on autism and genetic contributions to disease. In 2010, Neale wrote about the function of the hepatic lipase gene, LIPC.[7] The experiment found an association between advanced age-related macular degeneration (AMD), which is the main culprit of late onset blindness, and genetic variants in LIPC of the high-density lipoprotein cholesterol (HDL) pathway. The strongest association was found for rs10468017, which correlated with a protective, HDL-increasing effect of the T allele involved in AMD. Weaker associations were found for other LIPC loci ABCA1 and FADS1-3. The impact of this research lies in its examination of previously unthought-of pathways involved in the development of AMD.[citation needed]

In 2014, Neale contributed to a paper on the design of scientific disease studies focusing on uncommon genetic variants. The article included the operationalization of variables, advice on sample size, discussion of alleles and their frequencies, and information on noncoding and regions of the genome.[8]

That same year, he contributed on a paper examining the gene variant that allows for the experience of euphoria when taking d-amphetamine and connecting it to decreased risk for developing schizophrenia and ADHD.[9] In particular, the research found increased expression, or enrichment, of certain alleles associated with increased sensitivity to amphetamine-induced euphoria and decreased sensitivity to developing schizophrenia and ADHD. This work opens new possibilities to use the alleles that demonstrated changes in expression in order to analyze risk for developing neurological disorders that involve dopamine. Dopamine is the chemical in d-amphetamine that is responsible for its euphoric effects, and some disorders such as schizophrenia involve abnormal dopamine levels, though other factors are involved.[citation needed]

Neale has also researched influences on behaviors indicative of autism, namely that of de novo and familial factors.[10] The purpose of the study was to analyze IQ scores, assessments of behavior and language, spontaneous loss of function mutations, and familial history of mental illness. The study found a negative association between IQ scores and spontaneous loss of function mutation rates, and a positive association between IQ scores and family history of mental illness. This study suggests family history of mental illness could play a more influential role than previously thought in the phenotypic and genetic manifestations of autism.[citation needed]

In 2022, Neale co-published a study which linked potential genetic variants with bipolar disorder, saying "the long-term hope is that the genetic discoveries can form the basis of better understanding of the underlying biological processes that are involved in bipolar disorder".[11][12]

Awards[edit]

In 2016, Neale received the second Leena Peltonen Prize for Excellence in Human Genetics from the Paulo Foundation in Finland. Neale was given the award in recognition of his work in the fields of statistical and psychiatric genetics.[2] This has included research on the genetics of psychiatric disorders such as schizophrenia, major depression,[12][13] and autism.[14]

Personal life[edit]

Neale is openly gay.[15]

References[edit]

  1. ^ "The Editors". Statistical Genetics. Retrieved 2018-09-20.
  2. ^ a b "The second Leena Peltonen Prize for Excellence in Human Genetics to Dr. Benjamin Neale". EurekAlert! (Press release). 2016-03-03. Retrieved 2018-09-20.
  3. ^ a b "Benjamin Neale". Broad Institute. 2015-06-29. Retrieved 2018-09-20.
  4. ^ Purcell, Shaun; Neale, Benjamin; Todd-Brown, Kathe; Thomas, Lori; Ferreira, Manuel A.R.; Bender, David; Maller, Julian; Sklar, Pamela; De Bakker, Paul I.W.; Daly, Mark J.; Sham, Pak C. (2007-09-01). "PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses". The American Journal of Human Genetics. 81 (3): 559–575. doi:10.1086/519795. ISSN 0002-9297. PMC 1950838. PMID 17701901.
  5. ^ "Benjamin Neale". Broad Institute. 2015-06-29. Retrieved 2020-11-17.
  6. ^ Md 20852 (2020-07-13). "ASHG". ASHG. Retrieved 2020-11-17.{{cite web}}: CS1 maint: numeric names: authors list (link)
  7. ^ Neale, Benjamin (2010). "Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)". Proceedings of the National Academy of Sciences. 107 (16): 7396–7400. Bibcode:2010PNAS..107.7395N. doi:10.1073/pnas.0912019107. JSTOR 25665364. PMC 2867697. PMID 20385826.
  8. ^ Neale, Benjamin (January 28, 2014). "Searching for missing heritability: Designing rare variant association studies". Proceedings of the National Academy of Sciences. 111 (4): E455-64. Bibcode:2014PNAS..111E.455Z. doi:10.1073/pnas.1322563111. JSTOR 23769021. PMC 3910587. PMID 24443550.
  9. ^ Neale, Benjamin (April 22, 2014). "Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder". Proceedings of the National Academy of Sciences. 111 (16): 5968–5973. Bibcode:2014PNAS..111.5968H. doi:10.1073/pnas.1318810111. JSTOR 23771486. PMC 4000861. PMID 24711425.
  10. ^ Neale, Benjamin (October 21, 2014). "Autism spectrum disorder severity reflects the average contributions of de novo and familial influences". Proceedings of the National Academy of Sciences. 111 (42): 15161–15165. Bibcode:2014PNAS..11115161R. doi:10.1073/pnas.1409204111. JSTOR 43189895. PMC 4210299. PMID 25288738.
  11. ^ Cosgrove, Jonathan A.; Lu, Andrew M. (22 April 2022). "HMS and Broad Institute Researchers Discover First Strong Genetic Link to Bipolar Disorder | News | The Harvard Crimson". www.thecrimson.com. Retrieved 2023-11-21.
  12. ^ a b Makin, Simon (2014-10-16). "Schizophrenia's Genetic Roots". Scientific American Mind. 25 (6): 13. doi:10.1038/scientificamericanmind1114-13. Retrieved 2018-09-20.
  13. ^ "Same genes drive several psychiatric conditions, study says". UPI. 2018-06-22. Retrieved 2018-09-20.
  14. ^ Yong, Ed (2013-10-25). "Genetic Test for Autism Refuted". The Scientist Magazine. Retrieved 2018-09-20.
  15. ^ Belluck, Pam (2019-08-29). "Many Genes Influence Same-Sex Sexuality, Not a Single 'Gay Gene'". The New York Times. ISSN 0362-4331. Retrieved 2019-08-29.

External links[edit]

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