X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4623) 4623
Conference Proceeding (622) 622
Magazine Article (583) 583
Book Review (384) 384
Patent (280) 280
Publication (220) 220
Newspaper Article (186) 186
Book / eBook (159) 159
Book Chapter (119) 119
Reference (20) 20
Web Resource (20) 20
Dissertation (15) 15
Report (12) 12
Trade Publication Article (10) 10
Government Document (3) 3
Microfilm (3) 3
Paper (3) 3
Journal / eJournal (2) 2
Video Recording (2) 2
Data Set (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1469) 1469
humans (1382) 1382
female (713) 713
male (671) 671
clinical neurology (470) 470
aged (350) 350
middle aged (342) 342
abridged index medicus (338) 338
animals (324) 324
adult (305) 305
genetics & heredity (244) 244
research (215) 215
parkinson's disease (198) 198
old medline (196) 196
analysis (162) 162
surgery (157) 157
materials science, multidisciplinary (155) 155
medicine, general & internal (153) 153
neurosciences (152) 152
dementia (147) 147
child (138) 138
adolescent (128) 128
risk factors (128) 128
psychiatry (127) 127
physics, applied (125) 125
mutation (122) 122
physics (121) 121
aged, 80 and over (119) 119
chemistry (115) 115
biochemistry & molecular biology (114) 114
water resources (114) 114
diagnosis (112) 112
oncology (103) 103
mice (100) 100
article (97) 97
studies (91) 91
photography (90) 90
cinematography (86) 86
electrography (86) 86
holography (86) 86
risk (86) 86
chemistry, physical (85) 85
child, preschool (85) 85
parkinson disease - complications (85) 85
physics, condensed matter (85) 85
apparatus specially adapted therefor (84) 84
materials therefor (84) 84
originals therefor (84) 84
photomechanical production of textured or patterned surfaces,e.g. for printing, for processing of semiconductordevices (84) 84
metallurgy (83) 83
electricity (81) 81
phenotype (79) 79
alzheimers-disease (78) 78
basic electric elements (78) 78
engineering, civil (77) 77
molecular sequence data (77) 77
infant (75) 75
neurology (75) 75
pedigree (75) 75
rats (75) 75
time factors (75) 75
follow-up studies (74) 74
genetic aspects (73) 73
cancer (72) 72
semiconductor devices (72) 72
conjugated polymers (71) 71
light-emitting-diodes (70) 70
genetics (69) 69
cohort studies (68) 68
correspondence (68) 68
magnetic resonance imaging (68) 68
medical research (68) 68
multidisciplinary sciences (67) 67
united kingdom (67) 67
management (65) 65
electric solid state devices not otherwise provided for (64) 64
infant, newborn (64) 64
transporting (64) 64
usage (64) 64
geriatrics & gerontology (63) 63
performing operations (63) 63
environmental sciences (62) 62
care and treatment (61) 61
geosciences, multidisciplinary (61) 61
physiological aspects (61) 61
england (60) 60
parkinsons disease (60) 60
reviews (58) 58
history (57) 57
cell biology (56) 56
devices (56) 56
expression (56) 56
neuropsychological tests (56) 56
polymer science (56) 56
prevalence (56) 56
age factors (55) 55
amino acid sequence (55) 55
chemistry, multidisciplinary (55) 55
efficiency (55) 55
parkinson disease - diagnosis (55) 55
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (48) 48
UTL at Downsview - May be requested (29) 29
Gerstein Science - Stacks (27) 27
Online Resources - Online (26) 26
Collection Dvlpm't (Acquisitions) - Vendor file (12) 12
UofT at Scarborough - Stacks (12) 12
Thomas Fisher Rare Book - Rare Book (9) 9
Victoria University E.J. Pratt - Stacks (8) 8
Royal Ontario Museum - Stacks (7) 7
OISE - Stacks (6) 6
Trinity College (John W Graham) - Storage (6) 6
Media Commons - Microtexts (5) 5
UofT at Mississauga - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (4) 4
Law (Bora Laskin) - Stacks (4) 4
St. Michael's College (John M. Kelly) - 2nd Floor (4) 4
Engineering & Comp. Sci. - Stacks (3) 3
Massey College (Robertson Davies) - Rare Book (2) 2
Media Commons - Audio Visual (2) 2
Music - Stacks (2) 2
Royal Ontario Museum - Reference Desk (2) 2
Victoria University Emmanuel College - Storage (2) 2
Art - Deshman (1) 1
Art - Library use only (1) 1
Art - Reference (1) 1
Earth Sciences (Noranda) - Reference (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Faculty of Information - May be requested in 6-10 wks (1) 1
Faculty of Information - Stacks (1) 1
Gerstein Science - Bindery (1) 1
Gerstein Science - Missing (1) 1
Gerstein Science - Periodical Stacks (1) 1
Innis College - Stacks (1) 1
Knox College (Caven) - Stacks (1) 1
Law (Bora Laskin) - May be requested in 6-10 wks (1) 1
Law (Bora Laskin) - Reserve desk (1) 1
Map & Data - Map Collection (1) 1
New College (Ivey) - Stacks (1) 1
OISE - Curriculum Resources (1) 1
Richard Charles Lee Canada-Hong Kong - Library use only (1) 1
Robarts - Storage (1) 1
St. Augustine's Seminary - Stacks (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
Trinity College (John W Graham) - Oversize (1) 1
Trinity College (John W Graham) - Rare Book (1) 1
Trinity College (John W Graham) - SPCK (1) 1
UofT at Mississauga - Reference Oversize (1) 1
Victoria University E.J. Pratt - Rare Book (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6586) 6586
French (126) 126
German (30) 30
Chinese (12) 12
Spanish (12) 12
Korean (4) 4
Danish (3) 3
Japanese (3) 3
Norwegian (2) 2
Hungarian (1) 1
Italian (1) 1
Portuguese (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Annals of the American Association of Geographers, ISSN 2469-4452, 07/2017, Volume 107, Issue 4, pp. 998 - 1010
John Ross Mackay, President of the Association of American Geographers in 1969-1970, died peacefully on 28 October 2014. With his passing, the geographical and... 
GEOGRAPHY | Observers | Permafrost | Scientists | Research | Communities
Journal Article
Arctic, ISSN 0004-0843, 3/2015, Volume 68, Issue 1, pp. 129 - 131
  John Ross Mackay, Canada's pre-eminent authority on permafrost, died peacefully in the early morning of Oct 28, 2014. He was nearly 99 years old. Throughout... 
Obituary | ENVIRONMENTAL SCIENCES | GEOGRAPHY, PHYSICAL | Biography | Scientists | Geography | Science | Permafrost | Field study
Journal Article
Permafrost and Periglacial Processes, ISSN 1045-6740, 07/2017, Volume 28, Issue 3, pp. 513 - 516
No abstract is available for this article. 
LONG-TERM | GEOGRAPHY, PHYSICAL | WESTERN ARCTIC COAST | CANADA | AREA | GEOLOGY | ICE | Permafrost
Journal Article
Permafrost and Periglacial Processes, ISSN 1045-6740, 07/2017, Volume 28, Issue 3, pp. 513 - 516
Journal Article
by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | Index Medicus | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
by Nalls, Mike A and Pankratz, Nathan and Lill, Christina M and Do, Chuong B and Hernandez, Dena G and Saad, Mohamad and DeStefano, Anita L and Kara, Eleanna and Bras, Jose and Sharma, Manu and Schulte, Claudia and Keller, Margaux F and Arepalli, Sampath and Letson, Christopher and Edsall, Connor and Stefansson, Hreinn and Liu, Xinmin and Pliner, Hannah and Lee, Joseph H and Cheng, Rong and Ikram, M. Arfan and Ioannidis, John P. A and Hadjigeorgiou, Georgios M and Bis, Joshua C and Martinez, Maria and Perlmutter, Joel S and Goate, Alison and Marder, Karen and Fiske, Brian and Sutherland, Margaret and Xiromerisiou, Georgia and Myers, Richard H and Clark, Lorraine N and Stefansson, Kari and Hardy, John A and Heutink, Peter and Chen, Honglei and Wood, Nicholas W and Houlden, Henry and Payami, Haydeh and Brice, Alexis and Scott, William K and Gasser, Thomas and Bertram, Lars and Eriksson, Nicholas and Foroud, Tatiana and Singleton, Anew B and Plagnol, Vincent and Sheerin, Una-Marie and Simón-Sánchez, Javier and Lesage, Suzanne and Sveinbjörnsdóttir, Sigurlaug and Barker, Roger and Ben-Shlomo, Yoav and Berendse, Henk W and Berg, Daniela and Bhatia, Kailash and de Bie, Rob M. A and Biffi, Alessano and Bloem, Bas and Bochdanovits, Zoltan and Bonin, Michael and Bras, Jose M and Brockmann, Kathrin and Brooks, Janet and Burn, David J and Charlesworth, Gavin and Chinnery, Patrick F and Chong, Sean and Clarke, Carl E and Cookson, Mark R and Cooper, J. Mark and Corvol, Jean Christophe and Counsell, Carl and Damier, Philippe and Dartigues, Jean-François and Deloukas, Panos and Deuschl, Günther and Dexter, David T and van Dijk, Karin D and Dillman, Allissa and Durif, Frank and Dürr, Alexana and Edkins, Sarah and Evans, Jonathan R and Foltynie, Thomas and Dong, Jing and Gardner, Michelle and Gibbs, J. Raphael and Gray, Emma and Guerreiro, Rita and Harris, Clare and van Hilten, Jacobus J and Hofman, Albert and Hollenbeck, Albert and Holton, Janice and Hu, Michele and Huang, Xuemei and Wurster, Isabel and Mätzler, Walter and ... and GenePD and IPDG and Ashkenazi Jewish Dataset Investiga and 23AndMe and NABEC and HIHG and Greek Parkinson's Dis Consortium and GParkinson's Study Grp PSG Parkins and NGRC and Alzheimer Genetic Analysis Gr and CHARGE and UKBEC and Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and Hussman Institute of Human Genomics (HIHG) and 23andMe and Greek Parkinson's Disease Consortium and International Parkinson's Disease Genomics Consortium (IPDGC) and Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE) and United Kingdom Brain Expression Consortium (UKBEC) and NeuroGenetics Research Consortium (NGRC) and Ashkenazi Jewish Dataset Investigator and North American Brain Expression Consortium (NABEC) and Alzheimer Genetic Analysis Group and The Ashkenazi Jewish Dataset Investigator
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 9, pp. 989 - +
Journal Article
by Fitzgerald, T.W and Gerety, S.S and Jones, W.D and Van Kogelenberg, M and King, D.A and McRae, J and Morley, K.I and Parthiban, V and Al-Turki, S and Ambridge, K and Barrett, D.M and Bayzetinova, T and Clayton, S and Coomber, E.L and Gribble, S and Jones, P and Krishnappa, N and Mason, L.E and Middleton, A and Miller, R and Prigmore, E and Rajan, D and Sifrim, A and Tivey, A.R and Ahmed, M and Akawi, N and Andrews, R and Anjum, U and Archer, H and Armstrong, R and Balasubramanian, M and Banerjee, R and Baralle, D and Batstone, P and Baty, D and Bennett, C and Berg, J and Bernhard, B and Bevan, A.P and Blair, E and Blyth, M and Bohanna, D and Bourdon, L and Bourn, D and Brady, A and Bragin, E and Brewer, C and Brueton, L and Brunstrom, K and Bumpstead, S.J and Bunyan, D.J and Burn, J and Burton, J and Canham, N and Castle, B and Chandler, K and Clasper, S and Clayton-Smith, J and Cole, T and Collins, A and Collinson, M.N and Connell, F and Cooper, N and Cox, H and Cresswell, L and Cross, G and Crow, Y and D'Alessandro, M and Dabir, T and Davidson, R and Davies, S and Dean, J and Deshpande, C and Devlin, G and Dixit, A and Dominiczak, A and Donnelly, C and Donnelly, D and Douglas, A and Duncan, A and Eason, J and Edkins, S and Ellard, S and Ellis, P and Elmslie, F and Evans, K and Everest, S and Fendick, T and Fisher, R and Flinter, F and Foulds, N and Fryer, A and Fu, B and Gardiner, C and Gaunt, L and Ghali, N and Gibbons, R and Gomes Pereira, S.L and Goodship, J and Goudie, D and ... and Deciphering Dev Disorders Study and Deciphering Developmental Disorders Study and The Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 03/2015, Volume 519, Issue 7542, pp. 223 - 228
Despite three decades of successful, predominantly phenotype-driven discovery of the genetic causes of monogenic disorders(1), up to half of children with... 
INTELLECTUAL DISABILITY | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | MODEL | AUTISM SPECTRUM DISORDERS | COPY-NUMBER VARIATION | CHILDREN | Rare Diseases - genetics | Humans | Parents | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Dynamin I - genetics | Mutation, Missense - genetics | Polycomb Repressive Complex 1 - genetics | Gene Expression Regulation, Developmental | Transposases - genetics | Female | Nuclear Proteins - genetics | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Guanine Nucleotide Exchange Factors - genetics | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | United Kingdom | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Zebrafish - genetics | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Animals | Adolescent | Chromosome Aberrations | Genes, Dominant - genetics | Usage | Genomics | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Studies | Hypotheses | Genes | Developmental psychology | Families & family life | Genomes | Mutation | Children & youth | Index Medicus
Journal Article
Gut, ISSN 0017-5749, 07/2010, Volume 59, Issue 7, pp. 975 - 986
Peutz–Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic polyps throughout the gastrointestinal... 
ANNULAR TUBULES | VIDEO CAPSULE ENDOSCOPY | SEX CORD TUMOR | MUTATION CARRIERS | CLINICAL CHARACTERISTICS | FAMILIAL ADENOMATOUS POLYPOSIS | HEREDITARY COLORECTAL-CANCER | OF-THE-LI