المؤلفون: Jinkuk Hong, Robert S. Dembo, Leann Smith DaWalt, Mei Wang Baker, Elizabeth Berry-Kravis, Marsha R. Mailick

المصدر: Cells, Vol 12, Iss 17, p 2137 (2023)

مصطلحات موضوعية: FMR1 CGG repeats, mortality, higher education, differential sensitivity, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/12/17/2137; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/84212b94c74b4edfaaa220fa90e0ce1d

المؤلفون: Jinkuk Hong, Leann DaWalt, Mei Wang Baker, Elizabeth M. Berry-Kravis, Marsha R. Mailick

المصدر: Frontiers in Psychiatry, Vol 12 (2021)

مصطلحات موضوعية: FMR1 CGG repeats, genotype-phenotype associations, genetic epidemiology, population cohorts, normal genetic variation, Psychiatry, RC435-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fpsyt.2021.727085/full; https://doaj.org/toc/1664-0640

URL الوصول: https://doaj.org/article/758cf89a24dc456b96f8cde21cea5133

المؤلفون: Marsha R. Mailick, Jinkuk Hong, Leann Smith DaWalt, Jan S. Greenberg, Arezoo Movaghar, Mei Wang Baker, Paul J. Rathouz, Murray H. Brilliant

المصدر: Frontiers in Pediatrics, Vol 8 (2020)

مصطلحات موضوعية: FMR1 CGG repeats, gene x environment interactions, stressful parenting, trinucleotide repeat disorders, low zone genotype-phenotype associations, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fped.2020.00223/full; https://doaj.org/toc/2296-2360

URL الوصول: https://doaj.org/article/94e54bc9129e4949a87b4b2c7a65bc38

المؤلفون: Jinkuk, Hong, Leann, DaWalt, Mei Wang, Baker, Elizabeth M, Berry-Kravis, Marsha R, Mailick

المصدر: Frontiers in Psychiatry

مصطلحات موضوعية: Psychiatry, congenital, hereditary, and neonatal diseases and abnormalities, genetic epidemiology, population cohorts, FMR1 CGG repeats, genotype-phenotype associations, normal genetic variation, nervous system diseases, Original Research

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::611141115c100263d6be98a432375e35
https://pubmed.ncbi.nlm.nih.gov/34456771

المؤلفون: Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, Mei Wang Baker, Elizabeth M. Berry-Kravis, Murray H. Brilliant, Marsha Mailick

المصدر: American journal on intellectual and developmental disabilities. 128(1)

مصطلحات موضوعية: Psychiatry and Mental health, Neuropsychology and Physiological Psychology, Arts and Humanities (miscellaneous), Pediatrics, Perinatology and Child Health, Developmental and Educational Psychology, Neurology (clinical), General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98231cc91a34190e69aad30039e4c05f
https://pubmed.ncbi.nlm.nih.gov/36548377

المؤلفون: Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, Mei Wang Baker, Elizabeth M Berry-Kravis, Murray H. Brilliant, Marsha Mailick

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, nervous system diseases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fa755ac82e7fdd61d2b5ce0f143290f3
https://doi.org/10.21203/rs.3.rs-18291/v2

المؤلفون: Arezoo, Movaghar, David, Page, Murray, Brilliant, Mei Wang, Baker, Jan, Greenberg, Jinkuk, Hong, Leann Smith, DaWalt, Krishanu, Saha, Finn, Kuusisto, Ron, Stewart, Elizabeth, Berry-Kravis, Marsha R, Mailick

المصدر: Science Advances

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Heterozygote, SciAdv r-articles, nervous system diseases, Workflow, Fragile X Mental Retardation Protein, Phenotype, ROC Curve, Fragile X Syndrome, Population Surveillance, Databases, Genetic, Mutation, Genetics, Humans, Female, Genetic Predisposition to Disease, Genetic Association Studies, Research Articles, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::ad46f561894ed3bfb10c63530f8fd92a
https://pubmed.ncbi.nlm.nih.gov/31457090

المؤلفون: Richard H. Finnell, Huiping Zhu, Mei Wang Baker, Gary M. Shaw, Eric Neri, Edward J. Lammer

المصدر: American Journal of Medical Genetics. 108:1-6

مصطلحات موضوعية: Genetics, Pregnancy, education.field_of_study, business.industry, Offspring, Spina bifida, Population, Case-control study, Physiology, Odds ratio, medicine.disease, Genotype, Medicine, Risk factor, business, education, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e8f7a4393d31445e4f3652bd6f012972
https://doi.org/10.1002/ajmg.10195

المؤلفون: Gary M, Shaw, Edward J, Lammer, Huiping, Zhu, Mei Wang, Baker, Eric, Neri, Richard H, Finnell

المصدر: American journal of medical genetics. 108(1)

مصطلحات موضوعية: Oxidoreductases Acting on CH-NH Group Donors, Genotype, Infant, Newborn, Mutation, Missense, Membrane Proteins, Membrane Transport Proteins, Biological Transport, Polymorphism, Single Nucleotide, Folic Acid, Amino Acid Substitution, Pregnancy, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Carrier Proteins, Spinal Dysraphism, Methylenetetrahydrofolate Reductase (NADPH2)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::addfe8ee7a472abdce59d37e07245096
https://pubmed.ncbi.nlm.nih.gov/11857541

المؤلفون: Richard H. Finnell, Gary M. Shaw, Eric Neri, Mei Wang Baker, Huiping Zhu, Edward J. Lammer

المصدر: American Journal of Medical Genetics. 113:392-392

مصطلحات موضوعية: Vitamin, Genetics, chemistry.chemical_compound, medicine.medical_specialty, chemistry, Spina bifida, Reduced Folate Carrier, Genetic variation, medicine, Medical genetics, Biology, medicine.disease, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::542a983507fe153a3e3b58cb187d0dfd
https://doi.org/10.1002/ajmg.10986