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Journal of Exposure Science & Environmental Epidemiology
|
March 28, 2026
School-based exposures to oil and gas development for public school children in the United States
Cassandra J Clark, Erin Campbell, Stephanie T Grady, et al.
Molecular Genetics and Metabolism
|
June 14, 2008
CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency
Paul J Isackson, Michael J Bennett, Uta Lichter-Konecki, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
November 4, 2016
Dissonance-based eating disorder program reduces cardiac risk: A preliminary trial
Melinda A Green, Mary Willis, Kristen Fernandez-Kong, et al.
Environmental Epidemiology (Philadelphia, Pa.)
|
May 11, 2026
Warm season hourly temperature and psychiatric emergencies: A case-crossover study of a vulnerable population in Boston, 2005-2019
Kate Burrows, Flannery Black-Ingersoll, Nadav L Sprague, et al.
European Journal of Medical Genetics
|
September 21, 2022
Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes
Sabrina Neri, Nuno Maia, Ana M Fortuna, et al.
The Science of the Total Environment
|
February 25, 2025
A high resolution multipollutant assessment of health damages due to the onroad sector in Boston, Massachusetts
Manish Soni, Saravanan Arunachalam, M V S Ramarao, et al.
Environmental Health Perspectives
|
December 28, 2020
Community Approaches for Integrating Environmental Exposures into Human Models of Disease
Anne E Thessen, Cynthia J Grondin, Resham D Kulkarni, et al.
American Journal of Human Genetics
|
March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay
Valerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Journal of Medical Genetics
|
April 19, 2014
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
Kelly A Bear, Benjamin D Solomon, Sonir Antonini, et al.
American Journal of Human Genetics
|
February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
Federico Tessadori, Karen Duran, Karen Knapp, et al.
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Search research articles
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Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Journal of Exposure Science & Environmental Epidemiology
|
March 28, 2026
School-based exposures to oil and gas development for public school children in the United States
Cassandra J Clark, Erin Campbell, Stephanie T Grady, et al.
Molecular Genetics and Metabolism
|
June 14, 2008
CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency
Paul J Isackson, Michael J Bennett, Uta Lichter-Konecki, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
November 4, 2016
Dissonance-based eating disorder program reduces cardiac risk: A preliminary trial
Melinda A Green, Mary Willis, Kristen Fernandez-Kong, et al.
Environmental Epidemiology (Philadelphia, Pa.)
|
May 11, 2026
Warm season hourly temperature and psychiatric emergencies: A case-crossover study of a vulnerable population in Boston, 2005-2019
Kate Burrows, Flannery Black-Ingersoll, Nadav L Sprague, et al.
European Journal of Medical Genetics
|
September 21, 2022
Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes
Sabrina Neri, Nuno Maia, Ana M Fortuna, et al.
The Science of the Total Environment
|
February 25, 2025
A high resolution multipollutant assessment of health damages due to the onroad sector in Boston, Massachusetts
Manish Soni, Saravanan Arunachalam, M V S Ramarao, et al.
Environmental Health Perspectives
|
December 28, 2020
Community Approaches for Integrating Environmental Exposures into Human Models of Disease
Anne E Thessen, Cynthia J Grondin, Resham D Kulkarni, et al.
American Journal of Human Genetics
|
March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay
Valerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Journal of Medical Genetics
|
April 19, 2014
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
Kelly A Bear, Benjamin D Solomon, Sonir Antonini, et al.
American Journal of Human Genetics
|
February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
Federico Tessadori, Karen Duran, Karen Knapp, et al.
Page
of 3