X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (205) 205
Publication (31) 31
Conference Proceeding (18) 18
Book Chapter (7) 7
Book / eBook (1) 1
Dissertation (1) 1
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (91) 91
humans (82) 82
implicate (72) 72
male (41) 41
genes (34) 34
autism (33) 33
animals (32) 32
biochemistry & molecular biology (32) 32
de-novo mutations (31) 31
implicate order (28) 28
female (26) 26
genetic aspects (26) 26
analysis (24) 24
genetics (24) 24
genetics & heredity (24) 24
research (23) 23
article (22) 22
expression (19) 19
genomics (19) 19
schizophrenia (19) 19
variants (19) 19
genetic predisposition to disease (18) 18
prime implicates (18) 18
gene expression (17) 17
genomes (17) 17
mutation (17) 17
biology (15) 15
genome-wide association (15) 15
genotype (15) 15
neurosciences (15) 15
proteins (15) 15
middle aged (14) 14
prime implicate (14) 14
risk factors (14) 14
multidisciplinary sciences (13) 13
risk (13) 13
algorithms (12) 12
association (12) 12
autism spectrum disorder - genetics (12) 12
computer science, artificial intelligence (12) 12
genome-wide association study (12) 12
knowledge compilation (12) 12
mental disorders (12) 12
psychiatry (12) 12
adult (11) 11
cell biology (11) 11
gene (11) 11
gene-expression (11) 11
molecular sequence data (11) 11
network (11) 11
phenotype (11) 11
physiological aspects (11) 11
studies (11) 11
artificial intelligence (10) 10
autism spectrum disorder (10) 10
computer science (10) 10
isotope effects implicate (10) 10
mice (10) 10
pathways (10) 10
aged (9) 9
autism spectrum disorders (9) 9
disease (9) 9
health aspects (9) 9
identification (9) 9
implicates distinct functions (9) 9
intellectual disability (9) 9
polymorphism, single nucleotide - genetics (9) 9
protein (9) 9
screen implicates mirna-372 (9) 9
amino acid sequence (8) 8
child (8) 8
computer science, theory & methods (8) 8
consciousness (8) 8
deoxyribonucleic acid--dna (8) 8
diagnosis (8) 8
dna (8) 8
genetic research (8) 8
loci (8) 8
neurodevelopmental disorders (8) 8
polymorphism, single nucleotide (8) 8
prostatic neoplasms - genetics (8) 8
brain (7) 7
children (7) 7
clinical neurology (7) 7
complexity (7) 7
copy-number variation (7) 7
cytochrome p-450 enzyme system - chemistry (7) 7
developmental biology (7) 7
endocrinology & metabolism (7) 7
enzymes (7) 7
immunology (7) 7
models, molecular (7) 7
mutants implicate (7) 7
physics (7) 7
prime implicants (7) 7
signal transduction (7) 7
bacterial proteins - metabolism (6) 6
biophysics (6) 6
c-h hydroxylation (6) 6
cancer (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuron, ISSN 0896-6273, 09/2015, Volume 87, Issue 6, pp. 1215 - 1233
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 02/2015, Volume 100, Issue 2, pp. E333 - E344
Context: Disorders of sex development (DSD) are clinical conditions where there is a discrepancy between the chromosomal sex and the phenotypic (gonadal or... 
PROTEIN | GENE | ENDOCRINOLOGY & METABOLISM | GERMLINE MUTATIONS | MALE PSEUDOHERMAPHRODITISM | IMPLICATE | STEROIDOGENIC FACTOR-I | REVERSAL | Exome | 46, XY Disorders of Sex Development - genetics | Phenotype | 46, XY Disorders of Sex Development - diagnosis | Humans | Male | Genetic Testing - methods | Advances in Genetics | JCEM Online
Journal Article
Bioinformatics, ISSN 1367-4803, 09/2019, Volume 35, Issue 18, pp. 3433 - 3440
Abstract Motivation Whole exome sequencing (WES) studies for autism spectrum disorder (ASD) could identify only around six dozen risk genes to date because the... 
PATHWAYS | NETWORK | PROTEIN | BIOCHEMICAL RESEARCH METHODS | AUTISM SPECTRUM DISORDER | HAPLOINSUFFICIENCY | DE-NOVO MUTATIONS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | MATHEMATICAL & COMPUTATIONAL BIOLOGY | REGULATORS | EPILEPSY | DIFFERENTIATION | IMPLICATE
Journal Article
ACTA NEUROPATHOLOGICA, ISSN 0001-6322, 02/2019, Volume 137, Issue 2, pp. 209 - 226
Cardiovascular (CV)- and lifestyle-associated risk factors (RFs) are increasingly recognized as important for Alzheimer's disease (AD) pathogenesis. Beyond the... 
COMMON VARIANTS | Cardiovascular | Lipids | SCHIZOPHRENIA | Polygenic enrichment | PATHOLOGY | IDENTIFICATION | NEUROSCIENCES | CLINICAL NEUROLOGY | CHOLESTEROL-METABOLISM | Genetic pleiotropy | OVERLAP | PLEIOTROPY | TRAITS | Alzheimer's disease | ASSOCIATION | EXPRESSION | IMPLICATE
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2017, Volume 173, Issue 7, pp. 1951 - 1954
Developmental encephalopathies constitute a broad and genetically heterogeneous spectrum of disorders associated with global developmental delay, intellectual... 
epilepsy | developmental encephalopathy | PLXNA1 | AUTISM | DE-NOVO MUTATIONS | DUBOWITZ-SYNDROME | GENETICS & HEREDITY | IMPLICATE | Epilepsy
Journal Article
Ruan Jian Xue Bao/Journal of Software, ISSN 1000-9825, 08/2015, Volume 26, Issue 8, pp. 1937 - 1945
Journal Article
Cosmos and History, ISSN 1832-9101, 2016, Volume 12, Issue 2, pp. 137 - 149
Journal Article
Pediatric Neurology, ISSN 0887-8994, 09/2019, Volume 98, pp. 46 - 52
The current classification system of neurodevelopmental disorders is based on clinical criteria; however, this method alone fails to incorporate what is now... 
Autism spectrum disorders | Autism | Neurodevelopmental disorders | Molecular pathway | NETWORK | PROTEIN | GENES | BIOLOGY | CLASSIFICATION | PEDIATRICS | IMPLICATE | CLINICAL NEUROLOGY | Decision-making | Medicine, Experimental | Medical research | Genetics
Journal Article
Nature Neuroscience, ISSN 1097-6256, 08/2017, Volume 20, Issue 8, pp. 1043 - 1051
Journal Article