X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (91) 91
Newspaper Article (13) 13
Publication (10) 10
Book / eBook (4) 4
Book Review (3) 3
Conference Proceeding (1) 1
Dissertation (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (54) 54
humans (41) 41
female (27) 27
male (25) 25
article (21) 21
genomes (16) 16
research (16) 16
animals (14) 14
genetics & heredity (14) 14
genomics (14) 14
studies (14) 14
adult (12) 12
gene expression (12) 12
genetic aspects (12) 12
genes (11) 11
multidisciplinary sciences (10) 10
adolescent (9) 9
analysis (9) 9
autism (9) 9
genetic variation (9) 9
mutation (9) 9
phenotype (9) 9
cancer (8) 8
genetics (8) 8
middle aged (8) 8
brain (7) 7
child (7) 7
gene expression profiling (7) 7
genome-wide association (7) 7
proteins (7) 7
young adult (7) 7
aged (6) 6
causes of (6) 6
cell biology (6) 6
chromosomes (6) 6
disease (6) 6
expression (6) 6
gene rearrangement (6) 6
gene-expression (6) 6
mice (6) 6
physiological aspects (6) 6
tissues (6) 6
biochemistry & molecular biology (5) 5
bioinformatics (5) 5
copy number variation (5) 5
dna sequencing (5) 5
gene (5) 5
genetic research (5) 5
genome (5) 5
identification (5) 5
internal medicine (5) 5
medical colleges (5) 5
medical research (5) 5
neurosciences (5) 5
oncology (5) 5
pancreatic cancer (5) 5
sequence analysis, dna (5) 5
tennis (5) 5
translocation, genetic (5) 5
variants (5) 5
aged, 80 and over (4) 4
athletes (4) 4
child, preschool (4) 4
disease models, animal (4) 4
dna copy number variations (4) 4
exons (4) 4
framework (4) 4
genetic predisposition to disease (4) 4
genome, human - genetics (4) 4
genotype (4) 4
health aspects (4) 4
life sciences (4) 4
magnetic resonance imaging (4) 4
metastasis (4) 4
mutations (4) 4
neoplasms. tumors. oncology. including cancer and carcinogens (4) 4
neurodevelopmental disorders (4) 4
nucleotide sequencing (4) 4
organ specificity - genetics (4) 4
schizophrenia (4) 4
transcriptome (4) 4
adenocarcinoma - mortality (3) 3
behavioral disciplines and activities (3) 3
biological-tissue (3) 3
cell line (3) 3
cells (3) 3
cells, cultured (3) 3
chromosome breakpoints (3) 3
chromosome deletion (3) 3
chromosome inversion (3) 3
chromosome rearrangements (3) 3
chromothripsis (3) 3
computational biology (3) 3
computer simulation (3) 3
copy number variations (3) 3
deoxyribonucleic acid--dna (3) 3
developmental delay (3) 3
diagnosis (3) 3
diagnostic tests (3) 3
differentiation (3) 3
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


Genome Biology, ISSN 1474-7596, 06/2014, Volume 15, Issue 6, pp. R84 - R84
Journal Article
Nature Genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 5, pp. 692 - 699
Journal Article
Journal Article
01/2019, ISBN 9781392018682
Structural variants (SVs) are an important source of human genetic diversity but their contribution to traits, disease, and gene regulation remains unclear. In... 
Genetics | Biology | Bioinformatics
Dissertation
AIDS Research and Human Retroviruses, ISSN 0889-2229, 10/2018, Volume 34, Issue S1, pp. 1 - 407
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 1, pp. 36 - 45
Journal Article
by Barbeira, Alvaro N and Dickinson, Scott P and Bonazzola, Rodrigo and Zheng, Jiamao and Wheeler, Heather E and Torres, Jason M and Torstenson, Eric S and Shah, Kaanan P and Garcia, Tzintzuni and Edwards, Todd L and Stahl, Eli A and Huckins, Laura M and Aguet, François and Ardlie, Kristin G and Cummings, Beryl B and Gelfand, Ellen T and Getz, Gad and Hadley, Kane and Handsaker, Robert E and Huang, Katherine H and Kashin, Seva and Karczewski, Konrad J and Lek, Monkol and Li, Xiao and MacArthur, Daniel G and Nedzel, Jared L and Nguyen, Duyen T and Noble, Michael S and Segrè, Ayellet V and Trowbridge, Casandra A and Tukiainen, Taru and Abell, Nathan S and Balliu, Brunilda and Barshir, Ruth and Basha, Omer and Battle, Alexis and Bogu, Gireesh K and Brown, Andrew and Brown, Christopher D and Castel, Stephane E and Chen, Lin S and Chiang, Colby and Conrad, Donald F and Damani, Farhan N and Davis, Joe R and Delaneau, Olivier and Dermitzakis, Emmanouil T and Engelhardt, Barbara E and Eskin, Eleazar and Ferreira, Pedro G and Frésard, Laure and Gamazon, Eric R and Garrido-Martín, Diego and Gewirtz, Ariel D. H and Gliner, Genna and Gloudemans, Michael J and Guigo, Roderic and Hall, Ira M and Han, Buhm and He, Yuan and Hormozdiari, Farhad and Howald, Cedric and Jo, Brian and Kang, Eun Yong and Kim, Yungil and Kim-Hellmuth, Sarah and Lappalainen, Tuuli and Li, Gen and Li, Xin and Liu, Boxiang and Mangul, Serghei and McCarthy, Mark I and McDowell, Ian C and Mohammadi, Pejman and Monlong, Jean and Montgomery, Stephen B and Muñoz-Aguirre, Manuel and Ndungu, Anne W and Nobel, Andrew B and Oliva, Meritxell and Ongen, Halit and Palowitch, John J and Panousis, Nikolaos and Papasaikas, Panagiotis and Park, YoSon and Parsana, Princy and Payne, Anthony J and Peterson, Christine B and Quan, Jie and Reverter, Ferran and Sabatti, Chiara and Saha, Ashis and Sammeth, Michael and Scott, Alexandra J and Shabalin, Andrey A and Sodaei, Reza and Stephens, Matthew and Stranger, Barbara E and Strober, Benjamin J and Sul, Jae Hoon and ... and GTEx Consortium
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1825 - 20
Journal Article
by Li, Xin and Kim, Yungil and Tsang, Emily K and Davis, Joe R and Damani, Farhan N and Chiang, Colby and Hess, Gaelen T and Zappala, Zachary and Strober, Benjamin J and Scott, Alexandra J and Li, Amy and Ganna, Andrea and Bassik, Michael C and Merker, Jason D and Aguet, François and Ardlie, Kristin G and Cummings, Beryl B and Gelfand, Ellen T and Getz, Gad and Hadley, Kane and Handsaker, Robert E and Huang, Katherine H and Kashin, Seva and Karczewski, Konrad J and Lek, Monkol and Li, Xiao and MacArthur, Daniel G and Nedzel, Jared L and Nguyen, Duyen T and Noble, Michael S and Segrè, Ayellet V and Trowbridge, Casandra A and Tukiainen, Taru and Abell, Nathan S and Balliu, Brunilda and Barshir, Ruth and Basha, Omer and Bogu, Gireesh K and Brown, Andrew and Brown, Christopher D and Castel, Stephane E and Chen, Lin S and Conrad, Donald F and Cox, Nancy J and Delaneau, Olivier and Dermitzakis, Emmanouil T and Engelhardt, Barbara E and Eskin, Eleazar and Ferreira, Pedro G and Frésard, Laure and Gamazon, Eric R and Garrido-Martín, Diego and Gewirtz, Ariel D.H and Gliner, Genna and Gloudemans, Michael J and Guigo, Roderic and Hall, Ira M and Han, Buhm and He, Yuan and Hormozdiari, Farhad and Howald, Cedric and Im, Hae Kyung and Jo, Brian and Kang, Eun Yong and Kim-Hellmuth, Sarah and Lappalainen, Tuuli and Li, Gen and Liu, Boxiang and Mangul, Serghei and McCarthy, Mark I and McDowell, Ian C and Mohammadi, Pejman and Monlong, Jean and Muñoz-Aguirre, Manuel and Ndungu, Anne W and Nicolae, Dan L and Nobel, Andrew B and Oliva, Meritxell and Ongen, Halit and Palowitch, John J and Panousis, Nikolaos and Papasaikas, Panagiotis and Park, Yoson and Parsana, Princy and Payne, Anthony J and Peterson, Christine B and Quan, Jie and Reverter, Ferran and Sabatti, Chiara and Saha, Ashis and Sammeth, Michael and Shabalin, Andrey A and Sodaei, Reza and Stephens, Matthew and Stranger, Barbara E and Sul, Jae Hoon and Urbut, Sarah and Van De Bunt, Martijn and Wang, Gao and Wen, Xiaoquan and ... and GTEx Consortium and Leidos Biomedical—Project Management and NIH/NCI and Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group and Statistical Methods groups—Analysis Working Group and Biospecimen Collection Source Site—NDRI and NIH/NHGRI and Brain Bank Repository—University of Miami Brain Endowment Bank and Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California Santa Cruz and NIH Common Fund and Enhancing GTEx (eGTEx) groups and NIH/NIMH and Genome Browser Data Integration &Visualization—EBI and Biospecimen Collection Source Site—RPCI and Biospecimen Core Resource—VARI and ELSI Study and NIH/NIDA
Nature, ISSN 0028-0836, 10/2017, Volume 550, Issue 7675, pp. 239 - 243
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2011, Volume 89, Issue 4, pp. 551 - 563
Journal Article