X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (127) 127
humans (119) 119
ophthalmology (88) 88
female (68) 68
male (68) 68
glaucoma (61) 61
open-angle glaucoma (48) 48
glaucoma, open-angle - genetics (46) 46
middle aged (44) 44
eye diseases (41) 41
mutation (38) 38
genetics & heredity (37) 37
pedigree (36) 36
aged (34) 34
genetic structures (33) 33
sense organs (33) 33
adult (32) 32
eye proteins - genetics (29) 29
intraocular pressure (27) 27
article (26) 26
genetics (26) 26
genotype (23) 23
mutations (23) 23
polymorphism, single nucleotide (23) 23
risk factors (22) 22
abridged index medicus (21) 21
genetic predisposition to disease (21) 21
glycoproteins - genetics (21) 21
genetic aspects (20) 20
biochemistry & molecular biology (19) 19
genomes (19) 19
animals (18) 18
gene (18) 18
genome-wide association (18) 18
genes (17) 17
polymerase chain reaction (17) 17
aged, 80 and over (16) 16
cytoskeletal proteins (16) 16
genome-wide association study (16) 16
prevalence (16) 16
identification (15) 15
normal-tension glaucoma (15) 15
case-control studies (14) 14
common variants (14) 14
glaucoma - genetics (14) 14
intraocular-pressure (14) 14
mice (14) 14
phenotype (14) 14
research article (14) 14
adolescent (13) 13
analysis (13) 13
expression (13) 13
gene expression (13) 13
dna mutational analysis (12) 12
glaucoma, open-angle - diagnosis (12) 12
protein-serine-threonine kinases - genetics (12) 12
retina (12) 12
blindness (11) 11
disease (11) 11
gene frequency (11) 11
genetic linkage (11) 11
optic nerve (11) 11
research (11) 11
united-states (11) 11
genomics (10) 10
intraocular pressure - physiology (10) 10
macular degeneration (10) 10
multidisciplinary sciences (10) 10
alleles (9) 9
association (9) 9
central corneal thickness (9) 9
child (9) 9
low tension glaucoma - genetics (9) 9
optic disk - pathology (9) 9
visual fields (9) 9
amino acid sequence (8) 8
cohort studies (8) 8
cytoskeletal proteins - genetics (8) 8
eye (8) 8
genetic variation (8) 8
glaucoma, open-angle - metabolism (8) 8
health aspects (8) 8
immunohistochemistry (8) 8
medical colleges (8) 8
polymorphism, single-stranded conformational (8) 8
variants (8) 8
articles (7) 7
cells, cultured (7) 7
chromosome mapping (7) 7
degeneration (7) 7
disease models, animal (7) 7
exfoliation syndrome - genetics (7) 7
family (7) 7
gene mutations (7) 7
glaucoma, open-angle - physiopathology (7) 7
haplotypes (7) 7
linkage (7) 7
molecular sequence data (7) 7
optineurin (7) 7
poag (7) 7
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


JAMA Ophthalmology, ISSN 2168-6165, 01/2019, Volume 137, Issue 1, pp. 35 - 37
Mutations in the myocilin (MYOC) gene were discovered as a cause of primary open-angle glaucoma (POAG) in 1997. Twenty-one years later, mutations in MYOC... 
OPHTHALMOLOGY | IDENTIFICATION | Glaucoma | Heredity | Genetic disorders | Mutation | Ophthalmology | Genes
Journal Article
by Klionsky, Daniel J and Abdelmohsen, Kotb and Abe, Akihisa and Abedin, Md Joynal and Abeliovich, Hagai and Acevedo Arozena, Abraham and Adachi, Hiroaki and Adams, Christopher M and Adams, Peter D and Adeli, Khosrow and Adhihetty, Peter J and Adler, Sharon G and Agam, Galila and Agarwal, Rajesh and Aghi, Manish K and Agnello, Maria and Agostinis, Patrizia and Aguilar, Patricia V and Aguirre-Ghiso, Julio and Airoldi, Edoardo M and Ait-Si-Ali, Slimane and Akematsu, Takahiko and Akporiaye, Emmanuel T and Al-Rubeai, Mohamed and Albaiceta, Guillermo M and Albanese, Chris and Albani, Diego and Albert, Matthew L and Aldudo, Jesus and Algül, Hana and Alirezaei, Mehrdad and Alloza, Iraide and Almasan, Alexandru and Almonte-Beceril, Maylin and Alnemri, Emad S and Alonso, Covadonga and Altan-Bonnet, Nihal and Altieri, Dario C and Alvarez, Silvia and Alvarez-Erviti, Lydia and Alves, Sandro and Amadoro, Giuseppina and Amano, Atsuo and Amantini, Consuelo and Ambrosio, Santiago and Amelio, Ivano and Amer, Amal O and Amessou, Mohamed and Amon, Angelika and An, Zhenyi and Anania, Frank A and Andersen, Stig U and Andley, Usha P and Andreadi, Catherine K and Andrieu-Abadie, Nathalie and Anel, Alberto and Ann, David K and Anoopkumar-Dukie, Shailendra and Antonioli, Manuela and Aoki, Hiroshi and Apostolova, Nadezda and Aquila, Saveria and Aquilano, Katia and Araki, Koichi and Arama, Eli and Aranda, Agustin and Araya, Jun and Arcaro, Alexandre and Arias, Esperanza and Arimoto, Hirokazu and Ariosa, Aileen R and Armstrong, Jane L and Arnould, Thierry and Arsov, Ivica and Asanuma, Katsuhiko and Askanas, Valerie and Asselin, Eric and Atarashi, Ryuichiro and Atherton, Sally S and Atkin, Julie D and Attardi, Laura D and Auberger, Patrick and Auburger, Georg and Aurelian, Laure and Autelli, Riccardo and Avagliano, Laura and Avantaggiati, Maria Laura and Avrahami, Limor and Awale, Suresh and Azad, Neelam and Bachetti, Tiziana and Backer, Jonathan M and Bae, Dong-Hun and Bae, Jae-sung and Bae, Ok-Nam and Bae, Soo Han and Baehrecke, Eric H and Baek, Seung-Hoon and Baghdiguian, Stephen and Bagniewska-Zadworna, Agnieszka and ... and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Institutionen för medicin och hälsa and Avdelningen för läkemedelsforskning and Avdelningen för cellbiologi
Autophagy, ISSN 1554-8627, 01/2016, Volume 12, Issue 1, pp. 1 - 222
Journal Article
by Aung, T and Ozaki, M and Lee, M.C and Schlotzer-Schrehardt, U and Thorleifsson, G and Mizoguchi, T and Igo, R.P., Jr and Haripriya, A and Williams, S.E and Astakhov, Y.S and Orr, A.C and Burdon, K.P and Nakano, S and Mori, K and Abu-Amero, K and Hauser, M and Li, Z and Prakadeeswari, G and Bailey, J.N and Cherecheanu, A.P and Kang, J.H and Nelson, S and Hayashi, K and Manabe, S.I and Kazama, S and Zarnowski, T and Inoue, K and Irkec, M and Coca-Prados, M and Sugiyama, K and Jarvela, I and Schlottmann, P and Lerner, S.F and Lamari, H and Nilgun, Y and Bikbov, M and Park, K.H and Cha, S.C and Yamashiro, K and Zenteno, J.C and Jonas, J.B and Kumar, R.S.S and Perera, S.A and Chan, A.S.Y and Kobakhidze, N and George, R and Vijaya, L and Do, T and Edward, D.P and Juan Marcos, L. de and Pakravan, M and Moghimi, S and Ideta, R and Bach-Holm, D and Kappelgaard, P and Wirostko, B and Thomas, S and Gaston, D and Bedard, K and Greer, W.L and Yang, Z and Chen, X and Huang, L and Sang, J and Jia, H and Jia, L and Qiao, C and Zhang, H and Liu, X and Zhao, B and Wang, Y.X and Xu, L and Leruez, S and Reynier, P and Chichua, G and Tabagari, S and Uebe, S and Zenkel, M and Berner, D and Mossbock, G and Weisschuh, N and Hoja, U and Welge-Luessen, U.C and Mardin, C and Founti, P and Chatzikyriakidou, A and Pappas, T and Anastasopoulos, E and Lambropoulos, A and Ghosh, A and Shetty, R and Porporato, N and Saravanan, V and Venkatesh, R and Shivkumar, C and Kalpana, N and Sarangapani, S and Kanavi, M.R and Beni, A.N and Yazdani, S and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 7, pp. 993 - 1004
Exfoliation syndrome (XFS) is the most common known risk factor for secondary glaucoma and a major cause of blindness worldwide. Variants in two genes, LOXL1... 
INDIVIDUALS | RISK LOCI | PSEUDOEXFOLIATION SYNDROME | INFLAMMATORY-BOWEL-DISEASE | METAANALYSIS | POLYMORPHISMS | COMMON SEQUENCE VARIANTS | GENETICS & HEREDITY | GLAUCOMA | BLOOD-PRESSURE | GENOME-WIDE ASSOCIATION | Haplotypes | Humans | Asian Continental Ancestry Group - genetics | Extracellular Matrix - metabolism | Male | Gene Expression Profiling | Mutation, Missense | Amino Acid Oxidoreductases - genetics | Exfoliation Syndrome - ethnology | RNA, Messenger - biosynthesis | Aged, 80 and over | Female | Spheroids, Cellular | Calcium Channels - genetics | Molecular Chaperones - biosynthesis | Eye - metabolism | Genetic Predisposition to Disease | Genome-Wide Association Study | Amino Acid Oxidoreductases - physiology | Molecular Chaperones - genetics | Cell Adhesion | Point Mutation | Alleles | Exfoliation Syndrome - genetics | Amino Acid Substitution | Exfoliatins | Disease susceptibility | Genetic aspects | Analysis | Risk factors | Glaucoma | Genes | Principal components analysis | Cardiovascular disease | Genomes | Biology | Loci | Exfoliation | Studies | Collaboration | Blindness | Alzheimers disease | Index Medicus | Life Sciences | Populations and Evolution | Microbiology and Parasitology | Parasitology | Quantitative Methods | Computer Science | Genetics | Santé publique et épidémiologie | Bioinformatics | Human genetics | Virology
Journal Article
by Khor, Chiea Chuen and Do, Tan and Jia, Hongyan and Nakano, Masakazu and George, Ronnie and Abu-Amero, Khaled and Duvesh, Roopam and Chen, Li Jia and Li, Zheng and Nongpiur, Monisha E and Perera, Shamira A and Qiao, Chunyan and Wong, Hon-Tym and Sakai, Hiroshi and De Melo, Mônica Barbosa and Lee, Mei-Chin and SChan, Anita and Azhany, Yaakub and Dao, Thi Lam Huong and Ikeda, Yoko and Perez-Grossmann, Rodolfo A and Zarnowski, Tomasz and Day, Alexander C and Jonas, Jost B and Tam, Pancy O.S and Tran, Tuan Anh and Ayub, Humaira and Akhtar, Farah and Micheal, Shazia and Chew, Paul T.K and Aljasim, Leyla A and Dada, Tanuj and Luu, Tam Thi and Awadalla, Mona S and Kitnarong, Naris and Wanichwecharungruang, Boonsong and Aung, Yee Yee and Mohamed-Noor, Jelinar and Vijayan, Saravanan and Sarangapani, Sripriya and Husain, Rahat and Jap, Aliza and Baskaran, Mani and Goh, David and Su, Daniel H and Wang, Huaizhou and Yong, Vernon K and Yip, Leonard W and Trinh, Tuyet Bach and Makornwattana, Manchima and Nguyen, Thanh Thu and Leuenberger, Edgar U and Park, Ki-Ho and Wiyogo, Widya Artini and SKumar, Rajesh and Tello, Celso and Kurimoto, Yasuo and Thapa, Suman S and Pathanapitoon, Kessara and Salmon, John F and Sohn, Yong Ho and Fea, Antonio and Ozaki, Mineo and Lai, Jimmy S.M and Tantisevi, Visanee and Khaing, Chaw Chaw and Mizoguchi, Takanori and Nakano, Satoko and Kim, Chan-Yun and Tang, Guangxian and Fan, Sujie and Wu, Renyi and Meng, Hailin and Nguyen, Thi Thuy Giang and Tran, Tien Dat and Ueno, Morio and Martinez, Jose Maria and Ramli, Norlina and Aung, Yin Mon and Reyes, Rigo Daniel and Vernon, Stephen A and Fang, Seng Kheong and Xie, Zhicheng and Chen, Xiao Yin and Foo, Jia Nee and Sim, Kar Seng and Wong, Tina T and Quek, Desmond T and Venkatesh, Rengaraj and Kavitha, Srinivasan and Krishnadas, Subbiah R and Soumittra, Nagaswamy and Shantha, Balekudaru and Lim, Boon-Ang and Ogle, Jeanne and Vasconcellos, José P. Cde and Costa, Vital P and Abe, Ricardo Y and De Souza, Bruno B and Sng, Chelvin C and ...
Nature Genetics, ISSN 1061-4036, 05/2016, Volume 48, Issue 5, pp. 556 - 562
Journal Article