Search Filters
Format Format
Format Format
Sort by Item Count (A-Z)
Filter by Count
Journal Article (14) 14
Publication (4) 4
Dissertation (2) 2
Journal / eJournal (2) 2
Technical Report (2) 2
Book Chapter (1) 1
Conference Proceeding (1) 1
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
index medicus (9) 9
humans (8) 8
autism (6) 6
article (5) 5
female (5) 5
genetics & heredity (5) 5
research (5) 5
genetics (4) 4
genomics (4) 4
children (3) 3
comparative genomic hybridization (3) 3
genome (3) 3
genomes (3) 3
identification (3) 3
intellectual disability (3) 3
male (3) 3
polymorphism, single nucleotide (3) 3
abridged index medicus (2) 2
adult (2) 2
cells, cultured (2) 2
chromosomes (2) 2
chromosomes, human - genetics (2) 2
cognitive ability (2) 2
copy-number variants (2) 2
databases (2) 2
deoxyribonucleic acid--dna (2) 2
developmental delay (2) 2
developmental-disabilities (2) 2
disease (2) 2
dna microarrays (2) 2
genes (2) 2
genetic aspects (2) 2
genetic predisposition to disease (2) 2
genetic research (2) 2
genetic variation (2) 2
genome-wide association study (2) 2
heart (2) 2
medicine (2) 2
mental disorders (2) 2
mice (2) 2
mutation (2) 2
prenatal diagnosis (2) 2
risk factors (2) 2
risk loci (2) 2
seizures (2) 2
spectrum disorders (2) 2
susceptibility gene (2) 2
usage (2) 2
16q24.3 microdeletion (1) 1
6p deletion (1) 1
6p deletions (1) 1
abdominal-surgery (1) 1
adolescent (1) 1
age (1) 1
aged (1) 1
airbag systems (1) 1
algorithms (1) 1
alleles (1) 1
alzheimers-disease (1) 1
american-college (1) 1
analysis (1) 1
anesthesiology (1) 1
aneuploidy (1) 1
angiogenesis (1) 1
animals (1) 1
anterior-chamber (1) 1
array analysis (1) 1
array comparative genomic hybridization (1) 1
array-cgh (1) 1
association (1) 1
author (1) 1
author correction (1) 1
autism spectrum disorder (1) 1
autism spectrum disorder - genetics (1) 1
autism spectrum disorder - physiopathology (1) 1
autism spectrum disorder - psychology (1) 1
autism spectrum disorders (1) 1
autistic disorder - genetics (1) 1
autistic disorder - physiopathology (1) 1
autistic disorder - psychology (1) 1
base sequence (1) 1
behavioural genetics (1) 1
biochemistry (1) 1
biochemistry & molecular biology (1) 1
biochemistry, medical (1) 1
birth defects (1) 1
births (1) 1
ca super/calmodulin-dependent phosphodiesterase (1) 1
ca2 /calmodulin-dependent phosphodiesterase (1) 1
cag repeat (1) 1
cardiac surgical procedures (1) 1
cardiology (1) 1
cardiovascular diseases - genetics (1) 1
cardiovascular diseases - physiopathology (1) 1
cardiovascular malformations (1) 1
caregivers (1) 1
catholic church (1) 1
catholic church doctrines (1) 1
causation (1) 1
cell (1) 1
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

SAE technical paper series, Volume 2015-01-1473.
NHTSA issued the FMVSS 226 ruling in 2011. It established test procedures to evaluate countermeasures that can minimize the likelihood of a complete or partial... 
Six Sigma | Test procedures | Protective systems
SAE technical paper series, Volume 2011-01-0257.
This paper discusses steps for identifying, evaluating and recommending a quantifiable design metric or metrics for Side Airbag (SAB) development. Three... 
Design processes | Airbag systems
Communications Biology, ISSN 2399-3642, 12/2019, Volume 2, Issue 1
Journal Article
Communications biology, 2019, Volume 2, p. 97
[This corrects the article DOI: 10.1038/s42003-018-0226-0.]. 
Journal Article
by Deschamps, Alain and Hall, Richard and Grocott, Hilary and Mazer, C David and Choi, Peter T and Turgeon, Alexis F and de Medicis, Etienne and Bussières, Jean S and Hudson, Christopher and Syed, Summer and Seal, Doug and Herd, Stuart and Lambert, Jean and Denault, André and Deschamps, Alain and Mutch, Alan and Turgeon, Alexis and Denault, Andre and Todd, Andrea and Jerath, Angela and Fayad, Ashraf and Finnegan, Barry and Kent, Blaine and Kennedy, Brent and Cuthbertson, Brian H and Kavanagh, Brian and Warriner, Brian and MacAdams, Charles and Lehmann, Christian and Fudorow, Christine and McCartney, Colin and McIsaac, Dan and Dubois, Daniel and Campbell, David and Mazer, David and Neilpovitz, David and Rosen, David and Cheng, Davy and Drapeau, Dennis and Dillane, Derek and Tran, Diem and Mckeen, Dolores and Wijeysundera, Duminda and Jacobsohn, Eric and Couture, Etienne and Alam, Fahad and Abdallah, Faraj and Ralley, Fiona E and Chung, Frances and Lellouche, Francois and Dobson, Gary and Germain, Genevieve and Djaiani, George and Gilron, Ian and Hare, Gregory and Bryson, Gregory and Clarke, Hance and McDonald, Heather and Roman-Smith, Helen and Yang, Homer and Douketis, James and Paul, James and Beaubien, Jean and Bussières, Jean and Pridham, Jeremy and Armstrong, J N and Parlow, Joel and Murkin, John and Gamble, Jonathan and Duttchen, Kaylene and Karkouti, Keyvan and Turner, Kim and Baghirzada, Leyla and Szabo, Linda and Lalu, Manoj and Wasowicz, Marcin and Bautista, Michael and Jacka, Michael and Murphy, Michael and Schmidt, Michael and Verret, Michaël and Perrault, Michel-Antoine and Beaudet, Nicolas and Buckley, Norman and Choi, Peter and MacDougall, Peter and Jones, Philip and Drolet, Pierre and Beaulieu, Pierre and Taneja, Ravi and Martin, Rene and George, Ronald and Chun, Rosa and McMullen, Sarah and Beattie, Scott and Sampson, Sonia and Choi, Stephen and Kowalski, Stephen and McCluskey, Stuart and Boet, Sylvain and ... and Canadian Perioperative Anesthesia and Canadian Perioperative Anesthesia Clinical Trials Group
Anesthesiology, ISSN 0003-3022, 04/2016, Volume 124, Issue 4, pp. 826 - 836
Journal Article
by Roadmap Epigenomics Consortium, Epigenomics Consortium and Kundaje, Anshul and Meuleman, Wouter and Ernst, Jason and Bilenky, Misha and Yen, Angela and Heravi-Moussavi, Alireza and Kheradpour, Pouya and Zhang, Zhizhuo and Wang, Jianrong and Ziller, Michael J and Amin, Viren and Whitaker, John W and Schultz, Matthew D and Ward, Lucas D and Sarkar, Abhishek and Quon, Gerald and Sandstrom, Richard S and Eaton, Matthew L and Wu, Yi-Chieh and Pfenning, Andreas R and Wang, Xinchen and Claussnitzer, Melina and Liu, Yaping and Coarfa, Cristian and Harris, R. Alan and Shoresh, Noam and Epstein, Charles B and Gjoneska, Elizabeta and Leung, Danny and Xie, Wei and Hawkins, R. David and Lister, Ryan and Hong, Chibo and Gascard, Philippe and Mungall, Andrew J and Moore, Richard and Chuah, Eric and Tam, Angela and Canfield, Theresa K and Hansen, R. Scott and Kaul, Rajinder and Sabo, Peter J and Bansal, Mukul S and Carles, Annaick and Dixon, Jesse R and Farh, Kai-How and Feizi, Soheil and Karlic, Rosa and Kim, Ah-Ram and Kulkarni, Ashwinikumar and Li, Daofeng and Lowdon, Rebecca and Elliott, Ginell and Mercer, Tim R and Neph, Shane J and Onuchic, Vitor and Polak, Paz and Rajagopal, Nisha and Ray, Pradipta and Sallari, Richard C and Siebenthall, Kyle T and Sinnott-Armstrong, Nicholas A and Stevens, Michael and Thurman, Robert E and Wu, Jie and Zhang, Bo and Zhou, Xin and Beaudet, Arthur E and Boyer, Laurie A and De Jager, Philip L and Farnham, Peggy J and Fisher, Susan J and Haussler, David and Jones, Steven J. M and Li, Wei and Marra, Marco A and McManus, Michael T and Sunyaev, Shamil and Thomson, James A and Tlsty, Thea D and Tsai, Li-Huei and Wang, Wei and Waterland, Robert A and Zhang, Michael Q and Chadwick, Lisa H and Bernstein, Bradley E and Costello, Joseph F and Ecker, Joseph R and Hirst, Martin and Meissner, Alexander and Milosavljevic, Aleksandar and Ren, Bing and Stamatoyannopoulos, John A and Wang, Ting and Kellis, Manolis and Roadmap Epigenomics Consortium
Nature, ISSN 0028-0836, 02/2015, Volume 518, Issue 7539, pp. 317 - 329
Journal Article
by Burrage, Lindsay C and Reynolds, John J and Baratang, Nissan Vida and Phillips, Jennifer B and Wegner, Jeremy and McFarquhar, Ashley and Higgs, Martin R and Christiansen, Audrey E and Lanza, Denise G and Seavitt, John R and Jain, Mahim and Li, Xiaohui and Parry, David A and Raman, Vandana and Chitayat, David and Chinn, Ivan K and Bertuch, Alison A and Karaviti, Lefkothea and Schlesinger, Alan E and Earl, Dawn and Bamshad, Michael and Savarirayan, Ravi and Doddapaneni, Harsha and Muzny, Donna and Jhangiani, Shalini N and Eng, Christine M and Gibbs, Richard A and Bi, Weimin and Emrick, Lisa and Rosenfeld, Jill A and Postlethwait, John and Westerfield, Monte and Dickinson, Mary E and Beaudet, Arthur L and Ranza, Emmanuelle and Huber, Celine and Cormier-Daire, Valérie and Shen, Wei and Mao, Rong and Heaney, Jason D and Orange, Jordan S and Adams, David R and Aday, Aaron and Alejandro, Mercedes E and Allard, Patrick and Ashley, Euan A and Azamian, Mahshid S and Bacino, Carlos A and Baker, Eva and Balasubramanyam, Ashok and Barseghyan, Hayk and Batzli, Gabriel F and Beggs, Alan H and Behnam, Babak and Bellen, Hugo J and Bernstein, Jonathan A and Berry, Gerard T and Bican, Anna and Bick, David P and Birch, Camille L and Bonner, Devon and Boone, Braden E and Bostwick, Bret L and Briere, Lauren C and Brokamp, Elly and Brown, Donna M and Brush, Matthew and Burke, Elizabeth A and Burrage, Lindsay C and Butte, Manish J and Chen, Shan and Clark, Gary D and Coakley, Terra R and Cogan, Joy D and Colley, Heather A and Cooper, Cynthia M and Cope, Heidi and Craigen, William J and D’Souza, Precilla and Davids, Mariska and Davidson, Jean M and Dayal, Jyoti G and Dell’Angelica, Esteban C and Dhar, Shweta U and Dipple, Katrina M and Donnell-Fink, Laurel A and Dorrani, Naghmeh and Dorset, Daniel C and Douine, Emilie D and Draper, David D and Dries, Annika M and Duncan, Laura and Eckstein, David J and Emrick, Lisa T and Eng, Christine M and Enns, Gregory M and Eskin, Ascia and Esteves, Cecilia and Estwick, Tyra and Fernandez, Liliana and ... and University of Washington Center for Mendelian Genomics and Undiagnosed Diseases Network and Univ Washington Ctr Mendelian and Undiagnosed Dis Network
The American Journal of Human Genetics, ISSN 0002-9297, 03/2019, Volume 104, Issue 3, pp. 422 - 438
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 02/2013, Volume 21, Issue 2, pp. 173 - 181
Clinically significant cardiovascular malformations (CVMs) occur in 5-8 per 1000 live births. Recurrent copy number variations (CNVs) are among the known... 
cardiovascular malformations (CVMs) | protein-interaction network | Rare copy number variations | 16q24.3 microdeletion | extracardiac anomalies (ECAs) | GENOTYPE-PHENOTYPE CORRELATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEVELOPMENTAL DELAY | IDENTIFICATION | DIAPHRAGMATIC-HERNIA | ARRAY-CGH | DISEASE | GENETICS & HEREDITY | KBG SYNDROME | rare copy number variations | CONGENITAL HEART-DEFECTS | COMPARATIVE GENOMIC HYBRIDIZATION | CHROMOSOMAL-ABNORMALITIES | Sequence Deletion | Cardiovascular Diseases - physiopathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Aneuploidy | Male | DNA Copy Number Variations - genetics | Cardiovascular Diseases - genetics | Chromosomes, Human, Pair 22 - genetics | Eye Abnormalities | Protein Interaction Maps - genetics | Female | Polymorphism, Single Nucleotide | Chromosome Disorders - physiopathology | Chromosome Disorders - genetics | Chromosomes, Human, Pair 16 - genetics | Cohort Studies | Heart | Pediatrics | Congenital diseases | Ca2 /calmodulin-dependent phosphodiesterase | Copy number | Genes | Cognitive ability | Births | Genomes | Defects | Medicine | Studies | Nutrition research | Databases | Hospitals | Genetics | Mutation | Children | Cardiology | Deoxyribonucleic acid--DNA | Ca super(2+)/calmodulin-dependent phosphodiesterase | DNA | genomics | copy number
Journal Article
Cell Reports, ISSN 2211-1247, 08/2018, Volume 24, Issue 9, pp. 2506 - 2519
Retinal function relies on precisely organized neurons and synapses and a properly patterned vasculature to support them. Alterations in these features can... 
vasculature | nervous system | retina | neural disease | high-throughput screening | neuron | vision loss | synapse | GENE | ANGIOGENESIS | INFORMATION | DISEASE | MOUSE | MICE | IDENTIFICATION | EXPRESSION | CELL | GENOME | CELL BIOLOGY | Retina - physiology | Humans | Synapses | Neurons - physiology
Journal Article