المؤلفون: Shuran Yang, Qianyuan Li, Sheng Xiao, Jie Cheng, Quan He, Hongfei Zhang, Yujun Shao, Jirui He, Min Hu, Chenjiao Yao

المصدر: Environmental Research Communications, Vol 5, Iss 11, p 115018 (2023)

مصطلحات موضوعية: air pollution, cardiovascular disease, bibliometric, CiteSpace, VOSviewer, web of science, Environmental sciences, GE1-350, Meteorology. Climatology, QC851-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2515-7620

URL الوصول: https://doaj.org/article/6aafaef4833b4de88f2d02a8a9fcf48e

المؤلفون: Zizhu Zhang, Yizheng Chong, Yuanhao Liu, Jianji Pan, Cheng Huang, Qi Sun, Zhibo Liu, Xiayang Zhu, Yujun Shao, Congjun Jin, Tong Liu

المصدر: Cancers; Volume 15; Issue 16; Pages: 4060

مصطلحات موضوعية: BNCT, neutron source, boron agents, IHNI-1, NeuPex

وصف الملف: application/pdf

Relation: Cancer Therapy; https://dx.doi.org/10.3390/cancers15164060

الاتاحة: https://doi.org/10.3390/cancers15164060

المؤلفون: Yujun Shao, K. Decena, John R. Gilbert, Ruth K. Abramson, M. M. Menold, Chantelle M. Wolpert, Michael L. Cuccaro, Sarah A. Ravan, Elizabeth R. Hauser, Margaret A. Pericak-Vance, Harry H. Wright, L. Elston, G. R. DeLong, S. L. Donnelly, Kimberly L. Raiford

المصدر: The American Journal of Human Genetics. 72:539-548

مصطلحات موضوعية: Genetic Markers, Biometry, Genetic Linkage, Genes, Recessive, Locus (genetics), Biology, Genetic determinism, 03 medical and health sciences, Chromosome 15, 0302 clinical medicine, Gene mapping, Genetic linkage, Genetics, medicine, Humans, Family, Genetics(clinical), Autistic Disorder, Genetics (clinical), Genes, Dominant, 030304 developmental biology, Chromosome Aberrations, Chromosomes, Human, Pair 15, 0303 health sciences, Genetic heterogeneity, Chromosome Mapping, DNA, Articles, medicine.disease, Developmental disorder, Phenotype, Genetic marker, Multivariate Analysis, Lod Score, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c8d7b7b12befa242179bb802e1cf74
https://doi.org/10.1086/367846

المؤلفون: Sarah A. Ravan, Harry H. Wright, Margaret A. Pericak-Vance, Yujun Shao, S. L. Donnelly, Ruth K. Abramson, Chantelle M. Wolpert, Meredyth P. Bass, Michael L. Cuccaro

المصدر: Journal of Autism and Developmental Disorders. 33:87-91

مصطلحات موضوعية: Genetics, Proband, Genetic heterogeneity, medicine.disease, Genetic determinism, Developmental psychology, Developmental disorder, Race (biology), Neurodevelopmental disorder, Developmental and Educational Psychology, medicine, Etiology, Autism, Psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e25fb240b453ceddd5c80391ba22c40d
https://doi.org/10.1023/a:1022286622534

المؤلفون: Pinky A. McCoy, Yujun Shao, Sarah A. Ravan, Ruth K. Abramson, Harry H. Wright, Chantelle M. Wolpert, Heidi L. Abel, G. Robert DeLong, Margaret A. Pericak-Vance, Allison E. Ashley-Koch, Michael L. Cuccaro, John R. Gilbert, S. L. Donnelly

المصدر: American Journal of Medical Genetics. 114:106-109

مصطلحات موضوعية: Adult, Chromosome 7 (human), Genetics, Language Disorders, education.field_of_study, Adolescent, Population, Locus (genetics), Single-nucleotide polymorphism, Biology, medicine.disease, Wnt2 Protein, Neurodevelopmental disorder, Child, Preschool, Proto-Oncogene Proteins, Genotype, medicine, Humans, Autistic Disorder, Child, education, Allele frequency, Chromosomes, Human, Pair 7, Genetics (clinical), Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::373d4c5f7c8c3c53f5f0594d88e35186
https://doi.org/10.1002/ajmg.10182

المؤلفون: Yujun Shao, G. Robert DeLong, John R. Gilbert, Marisa M. Menold, Ruth K. Abramson, Michael L. Cuccaro, Kimberly L. Raiford, Chantelle M. Wolpert, Eden R. Martin, Sarah A. Ravan, S. L. Donnelly, Margaret A. Pericak-Vance, Harry H. Wright

المصدر: Journal of Neurogenetics. 15:245-259

مصطلحات موضوعية: Genetics, Chromosomes, Human, Pair 15, Linkage disequilibrium, Genotype, biology, GABAA receptor, GABRA5, Single-nucleotide polymorphism, Single-strand conformation polymorphism, Receptors, GABA-A, Polymorphism, Single Nucleotide, Molecular biology, Linkage Disequilibrium, Cellular and Molecular Neuroscience, Chromosome 15, biology.protein, Humans, Genetic Predisposition to Disease, Autistic Disorder, Polymorphism, Single-Stranded Conformational, GABRG3, Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab1b4226656c27cec1db14a7e004fdd5
https://doi.org/10.3109/01677060109167380

المؤلفون: Susan E. Folstein, John R. Gilbert, Jonathan L. Haines, Jacob L. McCauley, James S. Sutcliffe, James M. Jaworski, David A. Skaar, Margaret A. Pericak-Vance, Eden R. Martin, Jason H. Moore, Allison E. Ashley-Koch, Yujun Shao, Michael L. Cuccaro, G. R. DeLong, Judith E. Stenger

المصدر: Molecular psychiatry. 10(6)

مصطلحات موضوعية: Untranslated region, Male, Candidate gene, Genotype, Cell Adhesion Molecules, Neuronal, Single-nucleotide polymorphism, Nerve Tissue Proteins, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, White People, Cellular and Molecular Neuroscience, medicine, Humans, Genetic Predisposition to Disease, Autistic Disorder, Molecular Biology, Gene, Genetic association, Genetics, Chromosome 7 (human), Extracellular Matrix Proteins, Haplotype, Serine Endopeptidases, Infant, medicine.disease, Pedigree, Psychiatry and Mental health, Reelin Protein, Autism, Female, 5' Untranslated Regions, Chromosomes, Human, Pair 7

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff1a5c76cb8f94e164d9f56f30ce6899
https://pubmed.ncbi.nlm.nih.gov/15558079

المؤلفون: Kathleen A. Welsh-Bohmer, Charles E. Jackson, William K. Scott, P. C. Gaskell, Yujun Shao, J. B. Rimmler, Allison E. Ashley-Koch, Margaret A. Pericak-Vance, Jonathan L. Haines

المصدر: Neuroscience letters. 379(3)

مصطلحات موضوعية: Apolipoprotein E, Gerontology, Models, Molecular, Genetic Linkage, Population, Apolipoprotein E4, Apolipoproteins E, Genetic linkage, Alzheimer Disease, Ethnicity, Medicine, Dementia, Chromosomes, Human, Humans, Genetic Predisposition to Disease, Genetic Testing, Allele, education, Genetic testing, Genetics, Family Health, education.field_of_study, medicine.diagnostic_test, business.industry, General Neuroscience, Chromosome Mapping, medicine.disease, Human genetics, Pedigree, Genetic marker, Female, Lod Score, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9298f692a2d2673991c44bdb301688d2
https://pubmed.ncbi.nlm.nih.gov/15843063

المؤلفون: Margaret A. Pericak-Vance, Ruth K. Abramson, Kimberly L. Raiford, Eden R. Martin, Irving C. Allen, Michael L. Cuccaro, G. R. DeLong, Jeffery M. Vance, Harry H. Wright, Gordon Worley, M. M. Menold, John R. Gilbert, Yujun Shao

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)

مصطلحات موضوعية: Genetics, Gene isoform, Untranslated region, Apolipoprotein E, Male, Single-nucleotide polymorphism, Biology, medicine.disease, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Developmental disorder, Reelin Protein, Neurodevelopmental disorder, Apolipoproteins E, nervous system, Chromosome 19, medicine, Autism, Humans, lipids (amino acids, peptides, and proteins), Female, Genetic Predisposition to Disease, Autistic Disorder, Promoter Regions, Genetic, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f30320341cb93a4e122a4641a8997ae
https://pubmed.ncbi.nlm.nih.gov/14755445

المؤلفون: Michael L, Cuccaro, Yujun, Shao, Meredyth P, Bass, Ruth K, Abramson, Sarah A, Ravan, Harry H, Wright, Chantelle M, Wolpert, Shannon L, Donnelly, Margaret A, Pericak-Vance

المصدر: Journal of autism and developmental disorders. 33(1)

مصطلحات موضوعية: Male, Phenotype, Communication Disorders, Humans, Infant, Social Behavior Disorders, Stereotypic Movement Disorder, Female, Interpersonal Relations, Child Behavior Disorders, Autistic Disorder, Child

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0cf314418fa9e972f026ca1d43ce2a28
https://pubmed.ncbi.nlm.nih.gov/12708583

المؤلفون: John R. Gilbert, Sarah A. Ravan, Yujun Shao, Robert DeLong, Michael L. Cuccaro, Margaret A. Pericak-Vance, Kimberly L. Raiford, Harry H. Wright, Allison A. Ashley-Koch, Ruth K. Abramson, Chantelle M. Wolpert, Heidi Cope

مصطلحات موضوعية: Linkage disequilibrium, Genes, Recessive, Biology, Genetic determinism, Linkage Disequilibrium, Speech Disorders, 03 medical and health sciences, Genetic Heterogeneity, 0302 clinical medicine, Neurodevelopmental disorder, Report, medicine, Genetics, Humans, Genetics(clinical), Genetic Predisposition to Disease, Age of Onset, Autistic Disorder, Genetics (clinical), 030304 developmental biology, Genes, Dominant, Linkage (software), 0303 health sciences, Models, Genetic, Chromosome, Chromosome Mapping, medicine.disease, Phenotype, Developmental disorder, Chromosomes, Human, Pair 2, Autism, Lod Score, 030217 neurology & neurosurgery, Algorithms

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::384e5f6e90b3ed0d159b9ab7ec681ef7
https://europepmc.org/articles/PMC379103/

المؤلفون: Cate McClain, Kimberly L. Raiford, Margaret A. Pericak-Vance, Ruth H. Abramson, Michael L. Cuccaro, Jeffery M. Vance, S. L. Donnelly, Robert DeLong, Marisa M. Menold, Allison E. Ashley-Koch, Sarah A. Ravan, John R. Gilbert, Lennart von Wendt, Harry H. Wright, Meredyth P. Bass, Chantelle M. Wolpert, Yujun Shao

المصدر: American journal of medical genetics. 114(1)

مصطلحات موضوعية: Genetics, Adult, medicine.diagnostic_test, Genotype, Chromosome, Chromosome Mapping, Biology, medicine.disease, Centimorgan, Neurodevelopmental disorder, Chromosome 3, Genetic marker, Child, Preschool, medicine, Humans, Heritability of autism, Genetic Predisposition to Disease, Genetic Testing, Autistic Disorder, Lod Score, Genetics (clinical), X chromosome, Genetic testing, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb02894493c2d6903da08fbf2dca75b
https://pubmed.ncbi.nlm.nih.gov/11840513

المؤلفون: Silke Schmidt, Elizabeth R. Hauser, Eden R. Martin, William K. Scott, Yujun Shao, Susan H. Slifer, Marcy C. Speer, Margaret A. Pericak-Vance

المصدر: Genetic epidemiology. 21

مصطلحات موضوعية: 0301 basic medicine, Linkage (software), Structure (mathematical logic), Genotype, Models, Genetic, Epidemiology, Computer science, Association (object-oriented programming), Chromosome Mapping, 030105 genetics & heredity, computer.software_genre, Genome, Correlation, 03 medical and health sciences, 030104 developmental biology, Phenotype, Product (mathematics), Humans, Genetic Predisposition to Disease, Data mining, Genetic Testing, computer, Mathematical Computing, Genetics (clinical), Software

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::964bf66edfb58ae9aad77f282f6a2e45
https://pubmed.ncbi.nlm.nih.gov/11793734

المؤلفون: Bmc Genetics, Evadnie Rampersaud, Andrew Allen, Yi-ju Li, Yujun Shao, Meredyth Bass, Carol Haynes, Allison Ashley-koch, Eden R Martin, Silke Schmidt, Elizabeth R Hauser, Family Data, Complex Diseases, Christopher I Amos, Joan E Bailey-wilson, Rita M Cantor, Cashell E Jaquish, Maria Martinez, Rosalind J Neuman, Jane M

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/1b/a5/BMC_Genet_2003_Dec_31_4(Suppl_1)_S50.tar.gz

وصف الملف: application/zip

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.279.3372

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.279.3372

المؤلفون: Rampersaud, Evadnie, Allen, Andrew, Yi-Ju Li, Yujun Shao, Bass, Meredyth, Haynes, Carol, Ashley-Koch, Allison, Martin, Eden R., Schmidt, Silke, Hauser, Elizabeth R.

المصدر: BMC Genetics; 2003 Supplement 1, Vol. 4, pS50-7, 7p, 2 Charts, 2 Graphs

مصطلحات موضوعية: LINKAGE (Genetics), GENETIC research, GENEALOGY, GENETIC engineering, BLOOD pressure

المؤلفون: Yujun Shao, Elizabeth R. Hauser, Meredyth P. Bass, Eden R. Martin, Allison E. Ashley-Koch, Silke Schmidt, Evadnie Rampersaud, Yi-Ju Li, Andrew S. Allen, Carol Haynes

المصدر: BMC Genetics
Scopus-Elsevier
BMC Genetics, Vol 4, Iss Suppl 1, p S50 (2003)

مصطلحات موضوعية: Subset Analysis, Multifactorial Inheritance, lcsh:QH426-470, Chromosomes, Human, Pair 21, Genetic Linkage, Matched-Pair Analysis, Quantitative Trait Loci, Blood Pressure, Biology, Quantitative trait locus, 01 natural sciences, Genetic analysis, Time, 010104 statistics & probability, 03 medical and health sciences, Genetic linkage, Gene Order, Covariate, Genetics, Humans, Computer Simulation, Genetics(clinical), Longitudinal Studies, 0101 mathematics, Genetics (clinical), Chromosome 13, 0303 health sciences, Chromosomes, Human, Pair 13, Siblings, 030305 genetics & heredity, Chromosome Mapping, Contrast (statistics), lcsh:Genetics, Proceedings, Hypertension, Chromosomes, Human, Pair 5, Chromosomes, Human, Pair 7, Software, Type I and type II errors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac3977ceb9aa2211e55e19f39d50a0af