Yoo, A. J., Chaudhry, Z. A., Leslie-Mazwi, T. M., Chandra, R. V., Hirsch, J. A., González, R. G.
& Simonsen, C. Z. (2012).
Endovascular treatment of acute ischemic stroke: current indications.
Techniques in Vascular and Interventional Radiology,
15(1), 33-40.
https://doi.org/10.1053/j.tvir.2011.12.013
Yoo, A. J.
, Simonsen, C. Z., Prabhakaran, S., Chaudhry, Z. A., Issa, M. A., Fugate, J. E., Linfante, I., Liebeskind, D. S., Khatri, P., Jovin, T. G., Kallmes, D. F., Dabus, G., Zaidat, O. O. & Cerebral Angiographic Revascularization Grading Collaborators (2013).
Refining angiographic biomarkers of revascularization: Improving outcome prediction after intra-arterial therapy.
Stroke; a journal of cerebral circulation,
44(9), 2509-12.
https://doi.org/10.1161/STROKEAHA.113.001990
Yong, M.
, Thomsen, R. W., Schoonen, W. M.
, Farkas, D. K., Riis, A., Fryzek, J. P.
& Sørensen, H. T. (2010).
Mortality risk in splenectomised patients: a Danish population-based cohort study.
European Journal of Internal Medicine,
21(1), 12-6.
https://doi.org/10.1016/j.ejim.2009.10.003
Yong, M.
, Jensen, A. Ø., Jacobsen, J. B., Nørgaard, M., Fryzek, J. P.
& Sørensen, H. T. (2011).
Survival in breast cancer patients with bone metastases and skeletal-related events: a population-based cohort study in Denmark (1999-2007).
Breast Cancer Research and Treatment,
129(2), 495-503.
https://doi.org/10.1007/s10549-011-1475-5
Yong, M.
, Riis, A. H., Fryzek, J. P.
, Møller, B. K. & Johnsen, S. P. (2011).
Predictors and patterns of red blood cell transfusion use among newly diagnosed cancer patients with chemotherapy-associated anemia in Western Denmark (1998-2003).
Clinical Epidemiology,
3, 91-9.
https://doi.org/10.2147/CLEP.S17146
Yonehara, K., Fiscella, M., Drinnenberg, A., Esposti, F., Trenholm, S., Krol, J., Franke, F., Scherf, B. G., Kusnyerik, A., Müller, J., Szabo, A., Jüttner, J., Cordoba, F., Reddy, A. P., Németh, J., Nagy, Z. Z., Munier, F., Hierlemann, A. & Roska, B. (2016).
Congenital Nystagmus Gene FRMD7 Is Necessary for Establishing a Neuronal Circuit Asymmetry for Direction Selectivity.
Neuron,
89(1), 177-93.
https://doi.org/10.1016/j.neuron.2015.11.032
Yoakum, G. H., Korba, B. E., Lechner, J. F., Tokiwa, T., Gazdar, A. F., Seeley, T., Siegel, M., Leeman, L.
& Autrup, H. (1983).
High frequency transfection and cytopathology of the hepatitis B virus core antigen gene in human cells. Kexue (Shanghai),
222, 385-388.
Ylisaukko-oja, S. K., Cybulski, C., Lehtonen, R., Kiuru, M., Matyjasik, J., Szymañska, A., Szymañska-Pasternak, J.
, Andersen, L. D., Butzow, R.
, Ørntoft, T. F., Launonen, V., Lubiñski, J. & Aaltonen, L. A. (2006).
Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma.
European Journal of Human Genetics,
14, 880-883.
https://doi.org/10.1038/sj.ejhg.5201630
Ylinen, S., Uther, M., Latvala, A., Vepsäläinen, S., Iverson, P., Akahane-Yamada, R.
& Näätänen, R. (2010).
Training the brain to weight speech cues differently: a study of Finnish second-language users of English.
Journal of Cognitive Neuroscience,
22(6), 1319-32.
https://doi.org/10.1162/jocn.2009.21272
Ylinen, S., Nora, A.
, Leminen, A., Hakala, T., Huotilainen, M.
, Shtyrov, Y., Mäkelä, J. P. & Service, E. (2015).
Two distinct auditory-motor circuits for monitoring speech production as revealed by content-specific suppression of auditory cortex.
Cerebral Cortex,
25(6), 1576-86.
https://doi.org/10.1093/cercor/bht351
Ylijoki-Sørensen, S., Boldsen, J. L., Lalu, K., Sajantila, A., Baandrup, U.
, Boel, L. W. T., Ehlers, L. H. & Bøggild, H. (2014).
Cost-consequence analysis of cause of death investigation in Finland and in Denmark.
Forensic Science International,
245, 133-142.
https://doi.org/10.1016/j.forsciint.2014.10.032
Ylijoki-Sørensen, S., Boel, L. W. T., Boldsen, J. L., Bøggild, H., Lalu, K. & Sajantila, A. (2014).
Autopsy rate in suicide is low among elderly in Denmark compared with Finland.
Forensic Science International,
244, 158-165.
https://doi.org/10.1016/j.forsciint.2014.08.035
Ylijoki-Sørensen, S., Sajantila, A., Lalu, K., Bøggild, H., Boldsen, J. L.
& Boel, L. W. T. (2014).
Coding ill-defined and unknown cause of death is 13 times more frequent in Denmark than in Finland.
Forensic Science International,
244, 289-294.
https://doi.org/10.1016/j.forsciint.2014.09.016
Yland, J. J., Bresnick, K. A., Hatch, E. E., Wesselink, A. K.
, Mikkelsen, E. M., Rothman, K. J., Sørensen, H. T., Huybrechts, K. F.
& Wise, L. A. (2020).
Pregravid contraceptive use and fecundability: Prospective cohort study.
The BMJ,
371, Artikel 3966.
https://doi.org/10.1136/bmj.m3966
Yland, J. J., Crowe, H. M., Hatch, E. E., Willis, S. K., Wang, T. R.
, Mikkelsen, E. M., Savitz, D. A., Walkey, A. J., Rothman, K. J. & Wise, L. A. (2022).
A prospective study of preconception asthma and spontaneous abortion.
Annals of Epidemiology,
69, 27-33.
https://doi.org/10.1016/j.annepidem.2022.02.006
Ylä-Herttuala, S.
, Bentzon, J. F., Daemen, M.
, Falk, E., Garcia-Garcia, H. M., Herrmann, J., Hoefer, I., Jukema, J. W., Krams, R., Kwak, B. R., Marx, N., Naruszewicz, M., Newby, A., Pasterkamp, G., Serruys, P. W. J. C., Waltenberger, J., Weber, C. & Tokgözoglu, L. (2011).
Stabilisation of atherosclerotic plaques. Position paper of the European Society of Cardiology (ESC) Working Group on atherosclerosis and vascular biology.
Thrombosis and Haemostasis,
106(1), 1-19.
https://doi.org/10.1160/TH10-12-0784
Ylä-Herttuala, S.
, Bentzon, J. F., Daemen, M.
, Falk, E., Garcia-Garcia, H. M., Herrmann, J., Hoefer, I., Jauhiainen, S., Jukema, J. W., Krams, R., Kwak, B. R., Marx, N., Naruszewicz, M., Newby, A., Pasterkamp, G., Serruys, P. W. J. C., Waltenberger, J., Weber, C., Tokgözoglu, L. & ESC Working Group of Atherosclerosis and Vascular Biology (2013).
Stabilization of atherosclerotic plaques: an update.
European Heart Journal.
https://doi.org/10.1093/eurheartj/eht301
Yiu, G.
, Rasmussen, T. K., Ajami, B., Haddon, D. J., Chu, A. D., Tangsombatvisit, S., Haynes, W. A., Diep, V., Steinman, L., Faix, J. & Utz, P. J. (2016).
Development of Th17-Associated Interstitial Kidney Inflammation in Lupus-Prone Mice Lacking the Gene Encoding STAT-1.
Arthritis & Rheumatology,
68(5), 1233–1244.
https://doi.org/10.1002/art.39535
Yiu, G.
, Rasmussen, T. K., Tsai, B. L., Diep, V. K., Haddon, D. J., Tsoi, J., Miller, G. D., Comin-Anduix, B.
, Deleuran, B., Crooks, G. M. & Utz, P. J. (2022).
High Interferon Signature Leads to Increased STAT1/3/5 Phosphorylation in PBMCs From SLE Patients by Single Cell Mass Cytometry.
Frontiers in Immunology,
13, Artikel 833636.
https://doi.org/10.3389/fimmu.2022.833636
Yip, B. H. K., Leonard, H., Stock, S., Stoltenberg, C., Francis, R. W., Gissler, M., Gross, R.
, Schendel, D. & Sandin, S. (2017).
Caesarean section and risk of autism across gestational age: a multi-national cohort study of 5 million births.
International Journal of Epidemiology,
46(2), 429–439.
https://doi.org/10.1093/ije/dyw336
Yip, SY., Ruiz-Morales, J. M.
, Donskov, F., Fraccon, A. P., Basso, U., Rini, B. I., Lee, J.-L., Bjarnason, G. A., Sim, H.-W., Beuselinck, B., Kanesvaran, R., Brugarolas, J., Koutsoukos, K., Yuen Fai Fu, S., Yuasa, T., Davis, I. D., Alva, A., Kollmannsberger, C., Choueiri, T. K. & Heng, D. Y. C. (2017).
Outcomes of Metastatic Chromophobe Renal Cell Carcinoma (chrRCC) in the Targeted Therapy Era: Results from the International Metastatic Renal Cell Cancer Database Consortium (IMDC).
Kidney Cancer,
1(1), 41-47.
https://doi.org/10.3233/KCA-160002
Ying, L., Geleijns, J., Alvey, C., Benjamins, E., Chlapoutakis, K., Fraile Moreno, E.
, Hansen, J., Madsen, K. J. N. B., Meeson, S., Meijer, A., Niemann, T., Patel, R., Ruiz Lopez, L., Salmeron Berliz, I., Theocharopoulos, N., Bongartz, G., Calzado Cantera, A., Damilakis, J., Golding, S.
& Jurik, A. G. (2008).
WP1, Current practices of MSCT: a descriptive analysis. Poster session præsenteret på European Congress of Radiology, Wien, Østrig.
Yin, J., Hedayati, M., Grossman, L.
, Bolund, L. & Nexø, B. A. (2002).
Rapid genotying of human ERCC1 exon 4 polymorphism with fluorescence analysis using fluorophore-labelled hybridization probes and a lightCyclerTM.
Biochemical Genetics,
40, 143-148.
Yin, Y., Rockenbauer, E., Hedayati, M. A., Jacobsen, N. R., Vogel, U., Grossman, L.
, Bolund, L. & Nexø, B. A. (2002).
Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of basal cell carcinoma.
Cancer Epidemiology, Biomarkers, and Prevention,
11, 1449-1453.
Yin, J., Vogel, U.
, Gerdes, U., Dybdahl, M.
, Bolund, L. & Nexø, B. A. (2003).
Twelve single nucleotide polymorphisms on chromosome 19q13.2-3: Linkage disequilibria and associations with basal cell carcinoma in Danish psoriatic patients.
Biochemical Genetics,
1-2(41), 27-37.
Yin, D., Ling, S., Wang, D., Dai, Y., Jiang, H., Zhou, X.
, Paludan, S. R., Hong, J. & Cai, Y. (2021).
Targeting herpes simplex virus with CRISPR–Cas9 cures herpetic stromal keratitis in mice.
Nature Biotechnology,
39(5), 567-577.
https://doi.org/10.1038/s41587-020-00781-8
Yin, Y., Yakar, D., Dierckx, R. A. J. O.
, Mouridsen, K. B., Kwee, T. C. & de Haas, R. J. (2021).
Liver fibrosis staging by deep learning: a visual-based explanation of diagnostic decisions of the model.
European Radiology,
31(12), 9620-9627.
https://doi.org/10.1007/s00330-021-08046-x
Yin, Y., Yakar, D., Dierckx, R. A. J. O.
, Mouridsen, K. B., Kwee, T. C. & de Haas, R. J. (2022).
Combining Hepatic and Splenic CT Radiomic Features Improves Radiomic Analysis Performance for Liver Fibrosis Staging.
Diagnostics,
12(2), Artikel 550.
https://doi.org/10.3390/diagnostics12020550
Yilmaz, Z., Halvorsen, M., Bryois, J., Yu, D., Thornton, L. M., Zerwas, S., Micali, N., Moessner, R., Burton, C. L., Zai, G., Erdman, L., Kas, M. J., Arnold, P. D., Davis, L. K., Knowles, J. A., Breen, G., Scharf, J. M., Nestadt, G., Mathews, C. A. ... Eating Disorders Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive–Compulsive Disorder Working Group of the Psychiatric Genomics Consortium (2020).
Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder.
Molecular Psychiatry,
25(9), 2036-2046.
https://doi.org/10.1038/s41380-018-0115-4
Yilmaz, M., Sørensen, M. S.
, Sæbye, C., Baad-Hansen, T. & Petersen, M. M. (2019).
Long-term results of the Global Modular Replacement System tumor prosthesis for reconstruction after limb-sparing bone resections in orthopedic oncologic conditions: Results from a national cohort.
Journal of Surgical Oncology,
120(2), 183-192.
https://doi.org/10.1002/jso.25490
Yilmaz, Z., Schaumberg, K., Halvorsen, M., Goodman, E. L., Brosof, L. C., Crowley, J. J., Mathews, C. A.
, Mattheisen, M., Breen, G., Bulik, C. M., Micali, N., Zerwas, S. C. & Anorexia Nervosa Genetics Initiative (2023).
Predicting eating disorder and anxiety symptoms using disorder-specific and transdiagnostic polygenic scores for anorexia nervosa and obsessive-compulsive disorder.
Psychological Medicine,
53(7), 1-15.
https://doi.org/10.1017/S0033291721005079
Yilmaz, Z., Larsen, J. T., Nissen, J. B., Crowley, J. J.
, Mattheisen, M., Bulik, C. M.
& Petersen, L. V. (2022).
The role of early-life family composition and parental socio-economic status as risk factors for obsessive-compulsive disorder in a Danish national cohort.
Journal of Psychiatric Research,
149, 18-27.
https://doi.org/10.1016/j.jpsychires.2022.02.004
Yilmaz, Z., Quattlebaum, M. J., Pawar, P. S., Thornton, L. M., Bulik, C. M., Javaras, K. N., Yao, S., Lichtenstein, P., Larsson, H. & Baker, J. H. (2023).
Associations Between Attention Deficit Hyperactivity Disorder Symptom Dimensions and Disordered Eating Symptoms in Adolescence: A Population-Based Twin Study.
Behavior Genetics,
53(2), 143-153.
https://doi.org/10.1007/s10519-022-10128-5
Yıldız, Y.
, Olsen, R. K. J., Sivri, H. S., Akçören, Z.
, Nygaard, H. H. & Tokatlı, A. (2018).
Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy.
Neuromuscular Disorders,
28(9), 787-790.
https://doi.org/10.1016/j.nmd.2018.05.009
Yiallouris, A., Patrikios, I., Johnson, E. O., Sereti, E., Dimas, K., De Ford, C.
, Fedosova, N., Graier, W. F., Sokratous, K., Kyriakou, K. & Stephanou, A. (2018).
Annonacin promotes selective cancer cell death via NKA-dependent and SERCA dependent pathways.
Cell Death & Disease,
9(7), Artikel 764.
https://doi.org/10.1038/s41419-018-0772-x
Yi, X., Liang, Y., Huerta-Sanchez, E., Jin, X., Cuo, Z. X. P., Pool, J. E., Xu, X., Jiang, H., Vinckenbosch, N., Korneliussen, T. S., Zheng, H., Liu, T., He, W., Li, K., Luo, R., Nie, X., Wu, H., Zhao, M., Cao, H. ... Wang, J. (2010).
Sequencing of 50 human exomes reveals adaptation to high altitude.
Science,
329(5987), 75-8.
https://doi.org/10.1126/science.1190371
Yezli, S., Assiri, A., Nabulsi, H., Awam, A., Blumberg, L., Endericks, T., Stergachis, A., Reicher, S., McCloskey, B.
, Petersen, E., Alotaibi, B. & WHO Collaborating Centre on Mass Gatherings Medicine (2018).
From mass gatherings medicine to mass gatherings health: Conclusions from the 3rd International Conference on Mass Gatherings Medicine, Riyadh, Kingdom of Saudi Arabia.
International Journal of Infectious Diseases,
66, 128-130.
https://doi.org/10.1016/j.ijid.2017.12.019
Yeung, C.-H., Callies, C.
, Rojek, A., Nielsen, S. & Cooper, T. G. (2009).
Aquaporin Isoforms Involved in Physiological Volume Regulation of Murine Spermatozoa.
Biology of Reproduction,
80(2), 350-7.
https://doi.org/10.1095/biolreprod.108.071928
Yetley, E. A., Bailey, R. L., Sempos, C., Coates, P. M., Picciano, M. F., Pfeiffer, C. M., Phinney, K. W., Blackmore, S., Bock, J. L., Brody, L. C., Carmel, R., Curtin, L. R., Lacher, D. A., Johnson, C. L., Durazo-Arvizu, R. A., Eckfeldt, J. H., Green, R., Gregory III, J. F., Hoofnagle, A. N. ... Thorpe, S. J. (2011).
Biomarkers of vitamin B-12 status in NHANES: A roundtable summary.
American Journal of Clinical Nutrition,
94(1), 313-21.
https://doi.org/10.3945/ajcn.111.013243
Yetley, E. A., Pfeiffer, C. M., Phinney, K. W., Fazili, Z., Lacher, D. A., Bailey, R. L., Blackmore, S., Bock, J. L.
& Nexø, E. (2011).
Biomarkers of folate status in NHANES: a roundtable summary.
American Journal of Clinical Nutrition,
94(suppl), 303-12.
Yépez, V. A., Gusic, M., Kopajtich, R., Mertes, C., Smith, N. H., Alston, C. L., Ban, R., Beblo, S., Berutti, R., Blessing, H., Ciara, E., Distelmaier, F., Freisinger, P., Häberle, J., Hayflick, S. J., Hempel, M., Itkis, Y. S., Kishita, Y., Klopstock, T. ... Prokisch, H. (2022).
Clinical implementation of RNA sequencing for Mendelian disease diagnostics.
Genome Medicine,
14(1), Artikel 38.
https://doi.org/10.1186/s13073-022-01019-9
Yengo, L., Vedantam, S., Marouli, E., Sidorenko, J., Bartell, E., Sakaue, S., Graff, M., Eliasen, A. U., Jiang, Y., Raghavan, S., Miao, J., Arias, J. D., Graham, S. E., Mukamel, R. E., Spracklen, C. N., Yin, X., Chen, S.-H., Ferreira, T., Highland, H. H. ... Understanding Society Scientific Group (2022).
A saturated map of common genetic variants associated with human height.
Nature,
610(7933), 704–712.
https://doi.org/10.1038/s41586-022-05275-y