X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (196) 196
genetics & heredity (147) 147
article (128) 128
female (128) 128
index medicus (126) 126
male (124) 124
pedigree (97) 97
genetics (87) 87
genetic aspects (67) 67
mutation (57) 57
genetic linkage (51) 51
genotype (51) 51
research (50) 50
mutations (46) 46
genetic variation (45) 45
genes (43) 43
genomes (42) 42
adult (41) 41
phenotype (41) 41
chromosome mapping (40) 40
linkage analysis (40) 40
genetic predisposition to disease (38) 38
genomics (34) 34
lod score (34) 34
otorhinolaryngologic diseases (34) 34
middle aged (33) 33
genes, recessive (32) 32
haplotypes (32) 32
polymorphism, single nucleotide (32) 32
gene frequency (31) 31
deafness (30) 30
hearing loss - genetics (28) 28
child (27) 27
consanguinity (27) 27
risk factors (27) 27
disease (25) 25
gene (25) 25
pakistan (25) 25
adolescent (23) 23
alleles (23) 23
health aspects (23) 23
analysis (22) 22
animals (22) 22
biochemistry & molecular biology (22) 22
gene mutations (22) 22
aged (21) 21
human genetics (21) 21
human genome (21) 21
models, genetic (21) 21
studies (21) 21
exome (20) 20
genetic research (20) 20
genome-wide association study (20) 20
genotype & phenotype (20) 20
hearing impairment (20) 20
molecular sequence data (20) 20
physiological aspects (20) 20
research article (20) 20
sequence analysis, dna (20) 20
linkage disequilibrium (19) 19
base sequence (18) 18
genetic predisposition to disease - genetics (18) 18
homozygote (18) 18
mutation, missense (18) 18
mice (17) 17
microsatellite repeats (17) 17
multidisciplinary sciences (17) 17
program (17) 17
case-control studies (16) 16
genetic markers (16) 16
hearing loss (16) 16
identification (16) 16
proteins (16) 16
susceptibility (16) 16
expression (15) 15
family health (15) 15
genome-wide association (15) 15
linkage (15) 15
deoxyribonucleic acid--dna (14) 14
dna sequencing (14) 14
european continental ancestry group - genetics (14) 14
population (14) 14
quantitative trait, heritable (14) 14
aortic aneurysm, thoracic - genetics (13) 13
association (13) 13
biomedicine (13) 13
child, preschool (13) 13
methods (13) 13
molecular medicine (13) 13
nucleotide sequencing (13) 13
polymorphism, single nucleotide - genetics (13) 13
population genetics (13) 13
age of onset (12) 12
family (12) 12
maps (12) 12
phenotypes (12) 12
recombination (12) 12
report (12) 12
software (12) 12
amino acid sequence (11) 11
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLOS GENETICS, ISSN 1553-7390, 12/2007, Volume 3, Issue 12, pp. 2572 - 2573
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2008, Volume 83, Issue 3, pp. 311 - 321
Journal Article
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 10/2012, Volume 91, Issue 4, p. 585
  Next-generation sequencing has led to many complex-trait rare-variant (RV) association studies. Although single-variant association analysis can be... 
Genotype & phenotype | Genetic research | Heredity | Genetic testing | Estimating techniques | Genetic algorithms
Journal Article