Search Filters
Format Format
Format Format
Sort by Item Count (A-Z)
Filter by Count
Journal Article (242) 242
Publication (78) 78
Book / eBook (17) 17
Dissertation (10) 10
Conference Proceeding (5) 5
Book Chapter (4) 4
Newspaper Article (3) 3
Newsletter (2) 2
Book Review (1) 1
Web Resource (1) 1
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
humans (140) 140
female (104) 104
male (102) 102
index medicus (98) 98
genetics & heredity (88) 88
article (63) 63
pedigree (57) 57
mutation (42) 42
genetics (39) 39
genetic linkage (36) 36
middle aged (34) 34
polymorphism, single nucleotide (33) 33
risk factors (30) 30
genes (29) 29
adult (28) 28
deafness (27) 27
genotype (27) 27
aged (26) 26
animals (26) 26
genetic aspects (24) 24
genetic predisposition to disease (24) 24
phenotype (23) 23
association (21) 21
genomics (21) 21
biochemistry & molecular biology (20) 20
chromosome mapping (20) 20
cleft lip - genetics (20) 20
cleft palate - genetics (20) 20
research (20) 20
gene frequency (19) 19
hearing loss (19) 19
linkage (19) 19
mutations (19) 19
gene (18) 18
genes, dominant (18) 18
hispanic americans - genetics (18) 18
mice (18) 18
risk (18) 18
deafness - genetics (17) 17
carotid artery diseases - genetics (16) 16
child (16) 16
proteins (16) 16
alleles (15) 15
atherosclerosis (15) 15
disease (15) 15
family (15) 15
ischemic-stroke (15) 15
lod score (15) 15
otorhinolaryngologic diseases (15) 15
peripheral vascular disease (15) 15
research article (15) 15
analysis (14) 14
clinical neurology (14) 14
european continental ancestry group - genetics (13) 13
genetic markers (13) 13
genome-wide association study (13) 13
health aspects (13) 13
polymerase chain reaction (13) 13
polymorphism, single nucleotide - genetics (13) 13
population (13) 13
adolescent (12) 12
families (12) 12
genome-wide association (12) 12
molecular sequence data (12) 12
multidisciplinary sciences (12) 12
prevalence (12) 12
retinitis pigmentosa - genetics (12) 12
cohort studies (11) 11
dna mutational analysis (11) 11
expression (11) 11
genetic association studies (11) 11
genomes (11) 11
haplotypes (11) 11
human genetics (11) 11
carotid artery diseases - diagnostic imaging (10) 10
chromosomes (10) 10
dna (10) 10
gene mutations (10) 10
genetic predisposition to disease - genetics (10) 10
hearing impairment (10) 10
identification (10) 10
intima-media thickness (10) 10
medicine (10) 10
northern manhattan (10) 10
polymorphisms (10) 10
ultrasonography (10) 10
base sequence (9) 9
carotid intima-media thickness (9) 9
child, preschool (9) 9
deoxyribonucleic acid--dna (9) 9
epidemiology (9) 9
family health (9) 9
genetic research (9) 9
heritability (9) 9
history (9) 9
linkage analysis (9) 9
linkage disequilibrium (9) 9
stroke (9) 9
subclinical atherosclerosis (9) 9
united states (9) 9
Library Location Library Location
Library Location Library Location
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (10) 10
Collection Dvlpm't (Acquisitions) - Vendor file (4) 4
UofT at Mississauga - Stacks (3) 3
UTL at Downsview - May be requested (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Engineering & Comp. Sci. - Reference (1) 1
Gerstein Science - Stacks (1) 1
OISE - Stacks (1) 1
Online Resources - Online (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

Human Molecular Genetics, ISSN 0964-6906, 04/2019, Volume 28, Issue 8, pp. 1286 - 1297
Abstract Molecular mechanisms governing the development of the human cochlea remain largely unknown. Through genome sequencing, we identified a homozygous... 
Journal Article
Stroke, ISSN 0039-2499, 12/2013, Volume 44, Issue 12, pp. e236 - e236
Journal Article
Ethnicity and Disease, ISSN 1049-510X, 12/2017, Volume 27, Issue 1, pp. 11 - 14
Journal Article
International journal of audiology, ISSN 1499-2027, 07/2019, pp. 1 - 17
Universal newborn hearing screening (UNHS) uses otoacoustic emissions testing (OAE) and auditory brainstem response testing (ABR) to screen all newborn infants... 
Journal Article
Birth Defects Research Part A: Clinical and Molecular Teratology, ISSN 1542-0752, 09/2014, Volume 100, Issue 9, pp. 679 - 685
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2016, Volume 22, pp. 1239 - 1247
Purpose: To identify the underlying cause of disease in a large family with North Carolina macular dystrophy (NCMD). Methods: A large four-generation family... 
Journal Article
by Adams, H.H and Hibar, D.P and Chouraki, V and Stein, J.L and Nyquist, P.A and Renteria, M.E and Trompet, S and Arias-Vasquez, A and Seshai, S and Desrivieres, S and Beecham, A.H and Jahanshad, N and Wittfeld, K and Lee, S.J. van der and Abramovic, L and Alhusaini, S and Amin, N and Andersson, M and Arfanakis, K and Aribisala, B.S and Armstrong, N.J and Athanasiu, L and Axelsson, T and Beiser, A and Bernard, M and Bis, J.C and Blanken, L.M and Blanton, S.H and Bohlken, M.M and Boks, M.P and Bralten, J and Brickman, A.M and Carmichael, O and Chakravarty, M.M and Chauhan, G and Chen, Q and Ching, C.R and Cuellar-Partida, G and Braber, A.D and Doan, N.T and Ehrlich, S and Filippi, I and Ge, T and Giddaluru, S and Goldman, A.L and Gottesman, R.F and Greven, C.U and Grimm, O and Griswold, M.E and Guadalupe, T.M and Hass, J and Haukvik, U.K and Hilal, S and Hofer, E and Hoehn, D and Holmes, A.J and Hoogman, M and Janowitz, D and Jia, T and Kasperaviciute, D and Kim, S and Klein, M and Kraemer, B and Lee, P.H and Liao, J and Liewald, D.C and Lopez, L.M and Luciano, M and Macare, C and Marquand, A and Matarin, M and Mather, K.A and Mattheisen, M and Mazoyer, B and McKay, D.R and McWhirter, R and Milaneschi, Y and Mirza-Schreiber, N and Muetzel, R.L and Maniega, S.M and Nho, K and Nugent, A.C and Loohuis, L.M and Oosterlaan, J and Papmeyer, M and Pappa, I and Pirpamer, L and Pudas, S and Putz, B and Rajan, K.B and Ramasamy, A and Richards, J.S and Risacher, S.L and Roiz-Santianez, R and Rommelse, N and Rose, E.J and Royle, N.A and Rundek, T and Samann, P.G and Satizabal, C.L and ... and EPIGEN and SYS and Alzheimer's Dis Neuroimaging Initi and IMAGEN and Mind Research Network, Albuquerque, NM (United States) and Medicinska fakulteten and Institutionen för integrativ medicinsk biologi (IMB) and Umeå centrum för funktionell hjärnavbildning (UFBI) and Umeå universitet
Nature Neuroscience, ISSN 1097-6256, 2016, Volume 19, Issue 12, pp. 1569 - 1582
Journal Article
by Hibar, Derrek P and Adams, Hieab H. H and Jahanshad, Neda and Chauhan, Ganesh and Stein, Jason L and Hofer, Edith and Renteria, Miguel E and Bis, Joshua C and Arias-Vasquez, Alejano and Ikram, M. Kamran and Desrivières, Sylvane and Vernooij, Meike W and Abramovic, Lucija and Alhusaini, Saud and Amin, Najaf and Andersson, Micael and Arfanakis, Konstantinos and Aribisala, Benjamin S and Armstrong, Nicola J and Athanasiu, Lavinia and Axelsson, Tomas and Beecham, Ashley H and Beiser, Alexa and Bernard, Manon and Blanton, Susan H and Bohlken, Marc M and Boks, Marco P and Bralten, Janita and Brickman, Adam M and Carmichael, Owen and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher R. K and Chouraki, Vincent and Cuellar-Partida, Gabriel and Crivello, Fabrice and den Braber, Anouk and Doan, Nhat Trung and Ehrlich, Stefan and Giddaluru, Sudheer and Goldman, Aaron L and Gottesman, Rebecca F and Grimm, Oliver and Griswold, Michael E and Guadalupe, Tulio and Gutman, Boris A and Hass, Johanna and Haukvik, Unn K and Hoehn, David and Holmes, Avram J and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Jørgensen, Kjetil N and Karbalai, Nazanin and Kasperaviciute, Dalia and Kim, Sungeun and Klein, Marieke and Kraemer, Bernd and Lee, Phil H and Liewald, David C. M and Lopez, Lorna M and Luciano, Michelle and Macare, Christine and Marquand, Ane F and Matarin, Mar and Mather, Karen A and Mattheisen, Manuel and McKay, David R and Milaneschi, Yuri and Muñoz Maniega, Susana and Nho, Kwangsik and Nugent, Allison C and Nyquist, Paul and Loohuis, Loes M. Olde and Oosterlaan, Jaap and Papmeyer, Martina and Pirpamer, Lukas and Pütz, Benno and Ramasamy, Adaikalavan and Richards, Jennifer S and Risacher, Shannon L and Roiz-Santiañez, Roberto and Rommelse, Nanda and Ropele, Stefan and Rose, Emma J and Royle, Natalie A and Rundek, Tatjana and Sämann, Philipp G and Saremi, Arvin and Satizabal, Claudia L and Schmaal, Lianne and Schork, Anew J and Shen, Li and Shin, Jean and Shumskaya, Elena and Smith, Albert V and Sprooten, Emma and Strike, Lachlan T and Teumer, Alexander and ... and Medicinska fakulteten and Institutionen för integrativ medicinsk biologi (IMB) and Umeå centrum för funktionell hjärnavbildning (UFBI) and Umeå universitet
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, p. 13624
Journal Article
Stroke, ISSN 1524-4628, 01/2011, Volume 42, Issue 3, pp. 588 - 592
BACKGROUND AND PURPOSE{MDASH}: Sex differences have been recognized in stroke risk; however, the sex-dependent genetic contribution to stroke is unclear. We... 
Journal Article
Stroke, ISSN 1524-4628, 12/2010, Volume 41, Issue 12, pp. 2750 - 2756
BACKGROUND: and Purpose-Atherosclerosis is a complex subclinical cardiovascular disorder with a substantial genetic component. This study sought to identify... 
Journal Article
by Morris, Andrew P and Morris, Andrew P and Le, Thu H and Le, Thu H and Wu, Haojia and Akbarov, Artur and van der Most, Peter J and Hemani, Gibran and Hemani, Gibran and Smith, George Davey and Smith, George Davey and Mahajan, Anubha and Mahajan, Anubha and Gaulton, Kyle J and Gaulton, Kyle J and Nadkarni, Girish N and Nadkarni, Girish N and Valladares-Salgado, Adan and Valladares-Salgado, Adan and Wacher-Rodarte, Niels and Wacher-Rodarte, Niels and Mychaleckyj, Josyf C and Dueker, Nicole D and Guo, Xiuqing and Hai, Yang and Haessler, Jeffrey and Kamatani, Yoichiro and Kamatani, Yoichiro and Stilp, Adrienne M and Zhu, Gu and Zhu, Gu and Cook, James P and Ärnlöv, Johan and Blanton, Susan H and de Borst, Martin H and de Borst, Martin H and Bottinger, Erwin P and Bottinger, Erwin P and Buchanan, Thomas A and Buchanan, Thomas A and Cechova, Sylvia and Charchar, Fadi J and Chu, Pei-Lun and Damman, Jeffrey and Eales, James and Gharavi, Ali G and Gharavi, Ali G and Giedraitis, Vilmantas and Heath, Andrew C and Ipp, Eli and Ipp, Eli and Kiryluk, Krzysztof and Kiryluk, Krzysztof and Kramer, Holly J and Kramer, Holly J and Kubo, Michiaki and Kubo, Michiaki and Larsson, Anders and Lindgren, Cecilia M and Lu, Yingchang and Lu, Yingchang and Madden, Pamela A. F and Madden, Pamela A F and Montgomery, Grant W and Papanicolaou, George J and Raffel, Leslie J and Raffel, Leslie J and Sacco, Ralph L and Sacco, Ralph L and Sanchez, Elena and Sanchez, Elena and Stark, Holger and Sundstrom, Johan and Sundstrom, Johan and Taylor, Kent D and Xiang, Anny H and Xiang, Anny H and Zivkovic, Aleksandra and Lind, Lars and Ingelsson, Erik and Ingelsson, Erik and Martin, Nicholas G and Whitfield, John B and Whitfield, John B and Cai, Jianwen and Laurie, Cathy C and Okada, Yukinori and Okada, Yukinori and Matsuda, Koichi and Kooperberg, Charles and Chen, Yii-Der Ida and Rundek, Tatjana and Rundek, Tatjana and Rich, Stephen S and Rich, Stephen S and Loos, Ruth J F and Loos, Ruth J. F and Parra, Esteban J and Parra, Esteban J and Cruz, Miguel and ... and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature Communications, ISSN 2041-1723, 01/2019, Volume 10, Issue 1, pp. 29 - 14
Journal Article