X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (292) 292
Patent (7) 7
Book Chapter (3) 3
Publication (2) 2
Streaming Video (2) 2
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (186) 186
genetics & heredity (126) 126
female (120) 120
male (104) 104
child (61) 61
dna methylation (57) 57
genomic imprinting (46) 46
adult (44) 44
genetics (44) 44
phenotype (43) 43
adolescent (41) 41
child, preschool (40) 40
mutation (40) 40
beckwith-wiedemann syndrome - genetics (39) 39
infant (35) 35
epigenetics (34) 34
biochemistry & molecular biology (33) 33
methylation (32) 32
syndrome (32) 32
genes (30) 30
genetic aspects (30) 30
children (28) 28
cancer (27) 27
mutations (26) 26
research (26) 26
analysis (25) 25
beckwith-wiedemann syndrome (25) 25
expression (24) 24
gene (24) 24
pregnancy (24) 24
pediatrics (23) 23
pedigree (23) 23
autism (21) 21
chromosomes, human, pair 11 - genetics (20) 20
genomes (20) 20
infant, newborn (19) 19
animals (18) 18
beckwith-wiedemann-syndrome (18) 18
chromosomes, human, pair 11 (18) 18
gene expression (18) 18
genetic research (18) 18
dna (17) 17
epigenesis, genetic (17) 17
chromosome deletion (16) 16
genomics (16) 16
health aspects (16) 16
insulin-like growth factor ii - genetics (16) 16
sequence analysis, dna (16) 16
abnormalities, multiple - genetics (15) 15
chromosome mapping (15) 15
mice (15) 15
molecular sequence data (15) 15
risk factors (15) 15
chromosomes (14) 14
medical genetics (14) 14
cell line (13) 13
cpg islands (13) 13
in situ hybridization, fluorescence (13) 13
intellectual disability - genetics (13) 13
oncology (13) 13
wilms-tumor (13) 13
beckwith-wiedemann syndrome - diagnosis (12) 12
biotechnology & applied microbiology (12) 12
children's hospitals (12) 12
diagnosis (12) 12
genotype (12) 12
h19 (12) 12
overgrowth (12) 12
proteins (12) 12
tumors (12) 12
alleles (11) 11
base sequence (11) 11
chromosome aberrations (11) 11
development and progression (11) 11
gene mutations (11) 11
genetic disorders (11) 11
genomic imprinting - genetics (11) 11
imprinting (11) 11
middle aged (11) 11
risk (11) 11
schizophrenia (11) 11
chromatin (10) 10
dna - genetics (10) 10
igf2 (10) 10
in-vitro fertilization (10) 10
mental disorders (10) 10
microdeletion (10) 10
mosaicism (10) 10
patient (10) 10
uniparental disomy (10) 10
22q11 deletion syndrome (9) 9
beckwith-wiedemann syndrome - complications (9) 9
case-control studies (9) 9
chromosomes, human, pair 22 - genetics (9) 9
genetic predisposition to disease (9) 9
genetic testing (9) 9
growth (9) 9
human genetics (9) 9
hypomethylation (9) 9
individuals (9) 9
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 8, pp. 794 - 809
Objective Current research suggests that the causes of autism spectrum disorders (ASD) are multifactorial and include both genetic and environmental factors.... 
Pediatrics | Psychiatry | autism spectrum disorders | epigenetics | genetics | DNA METHYLATION | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | NEUROTROPHIC FACTOR BDNF | ANGELMAN-SYNDROME | UNIPARENTAL DISOMY | SEROTONIN TRANSPORTER GENE | RECEPTOR OXTR GENE | BECKWITH-WIEDEMANN-SYNDROME | FRAGILE-X-SYNDROME | LINKAGE-DISEQUILIBRIUM | PEDIATRICS | PRADER-WILLI-SYNDROME | Autism | Etiology | Pervasive Developmental Disorders | Mental Retardation | Evidence | Genetics | Environmental Influences | Cognitive Development | Symptoms (Individual Disorders) | Megalencephaly - psychology | Angelman Syndrome - psychology | Humans | Rett Syndrome - psychology | Angelman Syndrome - diagnosis | Social Environment | CHARGE Syndrome - psychology | Turner Syndrome - diagnosis | Prader-Willi Syndrome - psychology | Child Development Disorders, Pervasive - diagnosis | Angelman Syndrome - genetics | Prader-Willi Syndrome - genetics | Child | Fragile X Syndrome - genetics | Genetic Predisposition to Disease - psychology | Megalencephaly - genetics | Prader-Willi Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Genetic Association Studies | Rett Syndrome - diagnosis | Comorbidity | Risk Factors | CHARGE Syndrome - diagnosis | Chromosomes, Human, Pair 15 - genetics | Megalencephaly - diagnosis | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | Epigenesis, Genetic - genetics | Fragile X Syndrome - psychology | Adolescent | Turner Syndrome - genetics | CHARGE Syndrome - genetics | Rett Syndrome - genetics | Fragile X Syndrome - diagnosis | Psychological aspects | Epigenetic inheritance | Genetic aspects | Epigenetics | Child psychology | Gene expression | Genomics | Deoxyribonucleic acid--DNA
Journal Article
European journal of human genetics : EJHG, ISSN 1476-5438, 2009, Volume 18, Issue 1, pp. 8 - 14
Beckwith-Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigenesis. Unique observations in this... 
chromosome 11 | tumor predisposition | genomic imprinting | Beckwith-Wiedeman syndrome | epigenetics | METHYLATION | IMPRINTING CENTER | ABNORMALITIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | WILMS-TUMOR | TUMOR RISK | HYPOMETHYLATION | H19 | CHROMOSOME 11P15 | GENETICS & HEREDITY | LIT1 | MUTATIONS
Journal Article
The lancet oncology, ISSN 1470-2045, 2013, Volume 14, Issue 6, pp. 534 - 542
Journal Article
by C Yuen, Ryan K and Merico, Daniele and Bookman, Matt and L Howe, Jennifer and Thiruvahindrapuram, Bhooma and Patel, Rohan V and Whitney, Joe and Deflaux, Nicole and Bingham, Jonathan and Wang, Zhuozhi and Pellecchia, Giovanna and Buchanan, Janet A and Walker, Susan and Marshall, Christian R and Uddin, Mohammed and Zarrei, Mehdi and Deneault, Eric and D'Abate, Lia and Chan, Ada J S and Koyanagi, Stephanie and Paton, Tara and Pereira, Sergio L and Hoang, Ny and Engchuan, Worrawat and Higginbotham, Edward J and Ho, Karen and Lamoureux, Sylvia and Li, Weili and MacDonald, Jeffrey R and Nalpathamkalam, Thomas and Sung, Wilson W L and Tsoi, Fiona J and Wei, John and Xu, Lizhen and Tasse, Anne-Marie and Kirby, Emily and Van Etten, William and Twigger, Simon and Roberts, Wendy and Drmic, Irene and Jilderda, Sanne and Modi, Bonnie MacKinnon and Kellam, Barbara and Szego, Michael and Cytrynbaum, Cheryl and Weksberg, Rosanna and Zwaigenbaum, Lonnie and Woodbury-Smith, Marc and Brian, Jessica and Senman, Lili and Iaboni, Alana and Doyle-Thomas, Krissy and Thompson, Ann and Chrysler, Christina and Leef, Jonathan and Savion-Lemieux, Tal and Smith, Isabel M and Liu, Xudong and Nicolson, Rob and Seifer, Vicki and Fedele, Angie and Cook, Edwin H and Dager, Stephen and Estes, Annette and Gallagher, Louise and Malow, Beth A and Parr, Jeremy R and Spence, Sarah J and Vorstman, Jacob and Frey, Brendan J and Robinson, James T and Strug, Lisa J and Fernandez, Bridget A and Elsabbagh, Mayada and Carter, Melissa T and Hallmayer, Joachim and Knoppers, Bartha M and Anagnostou, Evdokia and Szatmari, Peter and Ring, Robert H and Glazer, David and Pletcher, Mathew T and Scherer, Stephen W
Nature neuroscience, ISSN 1546-1726, 2017, Volume 20, Issue 4, pp. 602 - 611
Journal Article
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 8, pp. 934 - 940
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 04/2018, Volume 103, Issue 4, pp. 1545 - 1557
... Martin Post,2,3 Alessandro Rolfo,1 Rosanna Weksberg,4 and Isabella Caniggia1,2,5 1Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario M5T... 
EARLY-ONSET PREECLAMPSIA | DNA METHYLATION | CERULOPLASMIN | ENDOCRINOLOGY & METABOLISM | TUMOR-SUPPRESSOR GENE | PLACENTAL DEVELOPMENT | IRON | HYPOXIA | EXPRESSION | RENAL-CARCINOMA | PREGNANCY | Chromatin | Animal models | Oxygen | Immunoprecipitation | Homeostasis | Iron | Pharmacology | Pre-eclampsia | Bioavailability | Gestation | Gene expression | Pregnancy | Control | Placenta | Preeclampsia | Epigenetics | Hypoxia | Mice | VHL protein | Supplementation
Journal Article
Epilepsia (Copenhagen), ISSN 0013-9580, 2015, Volume 56, Issue 5, pp. 707 - 716
Journal Article
Genetics in medicine, ISSN 1530-0366, 2017, Volume 20, Issue 4, pp. 435 - 443
Purpose: Genetic testing is an integral diagnostic component of pediatric medicine. Standard of care is often a time-consuming stepwise approach involving... 
diagnostics | copy number variation | next-generation sequencing | noncoding | whole-genome sequencing | SUCCESS | VARIANTS | MENDELIAN DISORDERS | AMERICAN-COLLEGE | MEDICAL GENETICS | IDENTIFICATION | INFANTS | GENETICS & HEREDITY | CAUSE INTELLECTUAL DISABILITY | MUTATIONS | CLINICAL EXOME | Pediatrics | Genes | Genomes | Original
Journal Article