X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (234) 234
female (166) 166
index medicus (145) 145
genetics & heredity (118) 118
mutation (104) 104
breast cancer (95) 95
breast neoplasms - genetics (86) 86
male (84) 84
risk factors (71) 71
adult (70) 70
middle aged (69) 69
oncology (69) 69
genetic aspects (67) 67
genetic predisposition to disease (64) 64
genetics (60) 60
genes (56) 56
research (51) 51
medical and health sciences (49) 49
medicin och hälsovetenskap (49) 49
genotype (47) 47
article (43) 43
cancer (43) 43
pedigree (43) 43
risk (42) 42
gene (40) 40
aged (39) 39
biochemistry & molecular biology (38) 38
genome-wide association (38) 38
polymorphism, single nucleotide (38) 38
alleles (36) 36
base sequence (35) 35
health aspects (35) 35
heterozygote (35) 35
cancer och onkologi (33) 33
phenotype (32) 32
cancer and oncology (31) 31
identification (31) 31
clinical medicine (30) 30
klinisk medicin (30) 30
mutations (30) 30
skin and connective tissue diseases (30) 30
expression (29) 29
genes, brca1 (29) 29
genes, brca2 (29) 29
tuberous sclerosis - genetics (29) 29
case-control studies (28) 28
molecular sequence data (28) 28
analysis (27) 27
genome-wide association study (27) 27
genomes (27) 27
dna mutational analysis (26) 26
gene mutations (26) 26
brca1 (25) 25
diagnosis (25) 25
brca1 protein - genetics (24) 24
child (24) 24
susceptibility (24) 24
tuberous sclerosis (24) 24
tumors (24) 24
ovarian-cancer (23) 23
polymerase chain reaction (23) 23
animals (21) 21
brca1 protein (21) 21
disease (21) 21
genetic variation (21) 21
polymorphism, single nucleotide - genetics (21) 21
tumor suppressor proteins - genetics (21) 21
adolescent (20) 20
breast neoplasms - pathology (20) 20
child, preschool (20) 20
congenital, hereditary, and neonatal diseases and abnormalities (20) 20
women (20) 20
dna (19) 19
epidemiology (19) 19
medicine & public health (19) 19
ovarian cancer (19) 19
research article (19) 19
common variants (18) 18
genetic predisposition to disease - genetics (18) 18
genetic testing (18) 18
medical research (18) 18
medicine (18) 18
polymorphism (18) 18
population (18) 18
brca2 protein (17) 17
breast (17) 17
medical genetics (17) 17
susceptibility loci (17) 17
tuberous sclerosis complex (17) 17
amino acid sequence (16) 16
chromosome mapping (16) 16
european continental ancestry group - genetics (16) 16
mutation - genetics (16) 16
odds ratio (16) 16
brca2 (15) 15
brca2 protein - genetics (15) 15
confer susceptibility (15) 15
genetic markers (15) 15
ovarian neoplasms - genetics (15) 15
prognosis (15) 15
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Gynecologic Oncology, ISSN 0090-8258, 2012, Volume 125, Issue 2, pp. 414 - 420
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 04/2014, Volume 51, Issue 4, pp. 245 - 253
Journal Article
Human mutation, ISSN 1059-7794, 2006, Volume 27, Issue 7, pp. 654 - 666
Journal Article
Journal Article
Journal Article
Genes, Chromosomes and Cancer, ISSN 1045-2257, 04/2016, Volume 55, Issue 4, pp. 350 - 354
In schwannomatosis, germline SMARCB1 or LZTR1 mutations predispose to the development of multiple benign schwannomas. Besides these, other tumors may occur in... 
MULTIPLE MENINGIOMAS | ONCOLOGY | GENETICS & HEREDITY | INI1/SMARCB1 | NF2 | MUTATIONS | SPECTRUM
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 2018, Volume 55, Issue 1, p. 15
Background We previously showed that the BRCA1 variant c.5096G>A p.Arg1699Gln (R1699Q) was associated with an intermediate risk of breast cancer (BC) and... 
Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
Journal Article
Journal Article