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Author Details
Full Name
Joel N Hirschhorn
Affiliation
Broad Institute of MIT and Harvard
ORCID
Career Start Year
1988
Papers
340
H Index
114
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37690116
Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome.
J Clin Endocrinol Metab
2024
38057443
Inferring compound heterozygosity from large-scale exome sequencing data.
Nat Genet
2024
37690116
Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome.
J Clin Endocrinol Metab
2024
38057443
Inferring compound heterozygosity from large-scale exome sequencing data.
Nat Genet
2024
36798175
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
bioRxiv
2023
37733769
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
PLoS Genet
2023
37987184
Phenotyping children and adolescents with obesity using behavioral, psychological, and familial data.
Obesity (Silver Spring)
2023
37214416
Corrigendum: Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank.
Front Genet
2023
37339320
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty.
J Clin Endocrinol Metab
2023
37443254
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases.
Nat Genet
2023
36993580
Inferring compound heterozygosity from large-scale exome sequencing data.
bioRxiv
2023
36798175
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
bioRxiv
2023
36685884
Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank.
Front Genet
2023
37228756
Genome-wide CRISPR screening of chondrocyte maturation newly implicates genes in skeletal growth and height-associated GWAS loci.
Cell Genom
2023
37292977
Genetics of skeletal proportions in two different populations.
bioRxiv
2023
37987184
Phenotyping children and adolescents with obesity using behavioral, psychological, and familial data.
Obesity (Silver Spring)
2023
37733769
Identification and analysis of individuals who deviate from their genetically-predicted phenotype.
PLoS Genet
2023
36993580
Inferring compound heterozygosity from large-scale exome sequencing data.
bioRxiv
2023
37214416
Corrigendum: Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank.
Front Genet
2023
37443254
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases.
Nat Genet
2023
37339320
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty.
J Clin Endocrinol Metab
2023
37228756
Genome-wide CRISPR screening of chondrocyte maturation newly implicates genes in skeletal growth and height-associated GWAS loci.
Cell Genom
2023
37292977
Genetics of skeletal proportions in two different populations.
bioRxiv
2023
36685884
Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank.
Front Genet
2023
34969092
Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome.
J Clin Endocrinol Metab
2022
35763030
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease.
Diabetologia
2022
35688811
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder.
Nat Commun
2022
35803701
Endocrine and behavioural features of Lowe syndrome and their potential molecular mechanisms.
J Med Genet
2022
35978186
Post-translational control of beige fat biogenesis by PRDM16 stabilization.
Nature
2022
36550108
Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.
Nat Commun
2022
34969092
Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome.
J Clin Endocrinol Metab
2022
35803701
Endocrine and behavioural features of Lowe syndrome and their potential molecular mechanisms.
J Med Genet
2022
35763030
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease.
Diabetologia
2022
35688811
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder.
Nat Commun
2022
36550108
Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.
Nat Commun
2022
35978186
Post-translational control of beige fat biogenesis by PRDM16 stabilization.
Nature
2022
32949984
Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
Blood Cells Mol Dis
2021
33901521
Racial and Ethnic Disparities in the Investigation and Treatment of Growth Hormone Deficiency.
J Pediatr
2021
33663556
The comparative effect of exposure to various risk factors on the risk of hyperuricaemia: diet has a weak causal effect.
Arthritis Res Ther
2021
33933144
Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study.
Clin Epigenetics
2021
33713608
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
2021
34346115
Genes with specificity for expression in the round cell layer of the growth plate are enriched in genomewide association study (GWAS) of human height.
J Bone Miner Res
2021
32989287
Genome-wide association study identifies 48 common genetic variants associated with handedness.
Nat Hum Behav
2021
33174594
Response to Letter to the Editor: "A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness".
J Clin Endocrinol Metab
2021
32949984
Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
Blood Cells Mol Dis
2021
34662877
Growth Hormone Stimulation Testing Patterns Contribute to Sex Differences in Pediatric Growth Hormone Treatment.
Horm Res Paediatr
2021
33713608
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
2021
33901521
Racial and Ethnic Disparities in the Investigation and Treatment of Growth Hormone Deficiency.
J Pediatr
2021
33663556
The comparative effect of exposure to various risk factors on the risk of hyperuricaemia: diet has a weak causal effect.
Arthritis Res Ther
2021
34662877
Growth Hormone Stimulation Testing Patterns Contribute to Sex Differences in Pediatric Growth Hormone Treatment.
Horm Res Paediatr
2021
1 - 50 of 680
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Collaborators
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Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
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Mark I McCarthy
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Erasmus University Medical Center
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Cecilia M Lindgren
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39
Eric Boerwinkle
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39
Cornelia M van Duijn
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39
Fernando Rivadeneira
University Medical Center Rotterdam
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38
Michael Boehnke
Co-authored papers
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Sailaja Vedantam
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38
Jing Hua Zhao
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38
Olli T Raitakari
Co-authored papers
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Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
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37
Andres Metspalu
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Brian E Henderson
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