X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (324) 324
Publication (68) 68
Paper (26) 26
Book / eBook (10) 10
Conference Proceeding (3) 3
Book Chapter (1) 1
Book Review (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
physics (54) 54
physics, particles & fields (47) 47
humans (45) 45
index medicus (42) 42
detector (40) 40
female (35) 35
male (31) 31
astrophysics (30) 30
astronomy & astrophysics (29) 29
lund monte-carlo (29) 29
fysik (28) 28
natural sciences (28) 28
naturvetenskap (28) 28
physical sciences (28) 28
experiment (27) 27
lep (27) 27
e+e annihilation (26) 26
jet fragmentation (25) 25
astronomy, astrophysics and cosmology (24) 24
genetics & heredity (24) 24
particle physics (24) 24
astronomi, astrofysik och kosmologi (23) 23
high energy astrophysical phenomena (23) 23
intellectual disability (23) 23
astroparticle physics (21) 21
astropartikelfysik (20) 20
child (19) 19
mutation (19) 19
adult (18) 18
particle physics - experiment (18) 18
physics - high energy astrophysical phenomena (18) 18
animals (17) 17
de-novo mutations (17) 17
leptons (17) 17
gene (16) 16
phenotype (16) 16
adolescent (15) 15
astrophysics - high energy astrophysical phenomena (15) 15
mutations (14) 14
z0 decays (14) 14
middle aged (13) 13
child, preschool (12) 12
e+e-physics (12) 12
emission (12) 12
expression (12) 12
genes (12) 12
intellectual disability - genetics (12) 12
radiative-corrections (12) 12
article (11) 11
decays (11) 11
opal experiment (11) 11
[phys.astr]physics [physics]/astrophysics [astro-ph] (10) 10
autism (10) 10
cosmology and extragalactic astrophysics (10) 10
family (10) 10
genetics (10) 10
proteins (10) 10
astronomy and astrophysics (9) 9
biochemistry & molecular biology (9) 9
energy (9) 9
fragmentation (9) 9
galaxy astrophysics (9) 9
gamma ray: vhe (9) 9
genetic aspects (9) 9
high-energies (9) 9
life sciences (9) 9
mice (9) 9
model (9) 9
analysis (8) 8
astronomy (8) 8
dna-binding proteins - genetics (8) 8
emissions (8) 8
gamma rays: general (8) 8
gammaover-bar (8) 8
infant (8) 8
intellectual disabilities (8) 8
radiation (8) 8
radiation mechanisms: non-thermal (8) 8
research (8) 8
simulation (8) 8
spectrum (8) 8
z decays (8) 8
aged (7) 7
bhabha scattering (7) 7
cosmic rays (7) 7
discovery (7) 7
mental-retardation (7) 7
opal detector (7) 7
phenotypes (7) 7
photon corrections (7) 7
physics, nuclear (7) 7
seizures (7) 7
transcription factors - genetics (7) 7
x-ray (7) 7
[ phys.astr ] physics [physics]/astrophysics [astro-ph] (6) 6
deletion (6) 6
developmental disabilities - genetics (6) 6
disease (6) 6
disorders (6) 6
epilepsy (6) 6
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


Human mutation, ISSN 1059-7794, 2019
Idiopathic intestinal varicosis is a developmental disorder defined by dilated and convoluted submucosal veins in the colon or small bowel. A limited number of... 
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 05/2012, Volume 18, Issue 10, pp. 2828 - 2837
Journal Article
Journal Article
International Journal of Cancer, ISSN 0020-7136, 03/2015, Volume 136, Issue 5, pp. E207 - E218
HPV‐related HNSCC generally have a better prognosis than HPV‐negative HNSCC. However, a subgroup of HPV‐positive tumors with poor prognosis has been... 
genetic localization | integration | viral integration | DIPS-PCR | APOT-PCR | APOT‐PCR | DIPS‐PCR | Integration | Genetic localization | Viral integration | SURVIVAL | HEAD | RISK-FACTORS | HUMAN-PAPILLOMAVIRUS TYPE-16 | PROGNOSIS | CERVICAL INTRAEPITHELIAL NEOPLASIA | HUMAN-PAPILLOMAVIRUS-16 DNA | NECK-CANCER | ONCOLOGY | HPV16 INTEGRATION | CARCINOMA | Receptor, Epidermal Growth Factor - genetics | Head and Neck Neoplasms - virology | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - pathology | Carcinoma, Squamous Cell - virology | Humans | Middle Aged | Male | Gene Expression Profiling | Immunoenzyme Techniques | Viral Load | Papillomavirus Infections - pathology | Human papillomavirus 16 - isolation & purification | Receptor, Epidermal Growth Factor - metabolism | Polymerase Chain Reaction | Female | Oncogene Proteins, Viral - genetics | Papillomavirus Infections - virology | Tumor Cells, Cultured | Virus Integration - genetics | In Situ Hybridization, Fluorescence | Head and Neck Neoplasms - pathology | Papillomavirus Infections - genetics | Head and Neck Neoplasms - genetics | DNA, Viral - genetics | Human papillomavirus 16 - genetics | Antiviral agents | Analysis | Genes | Genomics | Genetic research | Gene expression | Papillomavirus infections | Cervical cancer | Human papillomavirus | Genomes | Rodents | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
American Journal of Medical Genetics. Part A, ISSN 1552-4825, 2017, Volume 173, Issue 12, pp. 3238 - 3240
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2017, Volume 19, Issue 6, pp. 667 - 675
PURPOSE: Copy-number variation is a common source of genomic variation and an important genetic cause of disease. Microarray-based analysis of copy-number... 
read depth | exome sequencing | structural variation | Copy-number variants | diagnostic yield | QT SYNDROME | copy-number variants | SEVERE INTELLECTUAL DISABILITY | DEVELOPMENTAL DELAY | MODEL | POLYMORPHISM | CONGENITAL-ANOMALIES | GENOME | INSERTIONS | GENETICS & HEREDITY | MAP | Original
Journal Article
Plos Genetics, ISSN 1553-7404, 10/2017, Volume 13, Issue 10, p. e1006864
Kleefstra syndrome, caused by haploinsufficiency of euchromatin histone methyltransferase 1 (EHMT1), is characterized by intellectual disability (ID), autism... 
SUBTELOMERIC DELETION SYNDROME | MEMORY FORMATION | KLEEFSTRA SYNDROME | CONSTITUTIVE ANDROSTANE RECEPTOR | MOLECULAR CONVERGENCE | GENE-EXPRESSION | COMPASS FAMILY | DEVELOPMENTAL DELAY | ADULT DROSOPHILA-MELANOGASTER | NUCLEAR RECEPTOR | METHYLATION | MEMORY | GENETICS & HEREDITY | COURTSHIP | DROSOPHILA | DELETION | Cytoskeletal Proteins - genetics | Humans | Male | Craniofacial Abnormalities - physiopathology | Drosophila melanogaster - genetics | Intellectual Disability - genetics | Chromosomes, Human, Pair 9 - genetics | Heart Defects, Congenital - genetics | Neuronal Plasticity - genetics | Adult | Female | Child | Craniofacial Abnormalities - genetics | Chromosome Deletion | Autism Spectrum Disorder - genetics | Promoter Regions, Genetic | Histone-Lysine N-Methyltransferase - genetics | Gene Expression Regulation | Binding Sites - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Haploinsufficiency | Intellectual Disability - physiopathology | Animals | Histones - genetics | Adolescent | Heart Defects, Congenital - physiopathology | Drosophila Proteins - genetics | Mutation | Autism Spectrum Disorder - physiopathology | Physiological aspects | Histones | Methyltransferases | Mental retardation | Pervasive developmental disorders | Neurosciences | Transcription | Laboratories | Funding | Intellectual disabilities | Memory | Genes | Genomics | Disorders | Nervous system | Convergence | Euchromatin | Histone methyltransferase | Genetics | Life sciences | Bioinformatics | Protein families | Supervision | Medical research | Head | Developmental biology | Drosophila | Autism | Brain research | Plasticity (synaptic) | Cognition & reasoning | Insects | Short term memory | Binding sites
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2017, Volume 173, Issue 12, pp. 3238 - 3240
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 01/2017, Volume 100, Issue 1, pp. 91 - 104
Journal Article
Journal Article