The genomic landscape of UM-SCC oral cavity squamous cell carcinoma cell lines

by Birkeland, A.C, Brenner, J.C, Carey, T.E, Devenport, S.N, Foltin, S.K, Hoesli, R.C, Jewell, B.M, Jiang, H., Kulkarni, A., Ludwig, M.L, Mann, J.E, Michmerhuizen, N.L, Shuman, A.G, Spector, M.E
Published 2018

Frequent HPV-independent p16/INK4A overexpression in head and neck cancer

by Chakravarthy, A.R, Chester, K., Feber, A., Fenton, T.R, Forde, C.T, Forster, M., Hayes, D.N, Jay, A., Jones, T.M, Kalavrezos, N., Lechner, M., Masterson, L., McIndoe, R.A, O'Flynn, P., Vaz, F.M, Walter, V., Weinberger, P.M
Published 2018

Base of tongue cancer—is it tongue cancer located at the base of the tongue, or is it a type of lingual tonsil cancer? The perspective from a genomic analysis

by Choi, K.Y, Kim, J.H, Kim, K., Lee, D.J, Park, I.S, Rho, Y.S
Published 2018

Comparative genomic analysis of oral versus laryngeal and pharyngeal cancer

by van den Brekel, M.W.M, Vens, C., Verhagen, C.V.M, Verheij, M., Vossen, D.M, Wessels, L.F.A
Published 2018

Prenatal genetic testing in 19 fetuses with corpus callosum abnormality

by Peng, C., She, Q., Tan, W., Tang, E., Wang, D., Wang, L.
Published 2021

Prediction of Synthetic Lethal Interactions in Human Cancers Using Multi-View Graph Auto-Encoder

by Cai, R., Fang, Y., Hao, Z., Li, X., Wu, D., Wu, M.
Published 2021

Exploring the Genomic Landscape of Cancer Patient Cohorts with GenVisR

by Campbell, K.M, Cotto, K.C, Griffith, M., Griffith, O.L, Skidmore, Z.L
Published 2021

Generating CRISPR-Cas9-Mediated Null Mutations and Screening Targeting Efficiency in Human Pluripotent Stem Cells

by Alanis-Lobato, G., Bower, O.J, Gerri, C., Lea, R.A, McCarthy, A., Niakan, K.K, Turner, J.M.A, Zohren, J.
Published 2021

Association of DYNC1H1 gene SNP/CNV with disease susceptibility, GCs efficacy, HRQOL, anxiety, and depression in Chinese SLE patients

by Cai, J., Chen, Y., Huang, H., Huang, S., Li, M., Li, Z., Liu, S., Lou, Q., Teng, Y., Wang, L., Wang, Y., Xu, Z., Yan, Z., Zhang, T., Zou, Y.
Published 2021

Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center

by Cai, M., Fu, X., Huang, H., Lin, N., Su, L., Wu, X., Xie, X., Xu, L., Xu, S.
Published 2022

Distinct diagnostic trajectories in NBAS-associated acute liver failure highlights the need for timely functional studies

by Akesson, L.S, Amarasekera, S., Bordador, E., Brown, N.J, Chai, C., Chong, B., Christodoulou, J., Compton, A.G, Donoghue, S., Guo, Y., Hakonarson, H., Lee, C., Lunke, S., Marum, J., Monaco, A., Rius, R., Rosenbaum, J., Stark, Z., Stormon, M., Thorburn, D.R
Published 2022

ggComp enables dissection of germplasm resources and construction of a multiscale germplasm network in wheat

by Chai, L., Feng, X., Guo, W., Hu, Z., Li, J., Liang, R., Liu, J., Ni, Z., Peng, H., Su, Z., Sun, Q., Wang, W., Wang, X., Wang, Z., Xie, X., Xin, M., Yang, Z., Yao, Y., You, M.
Published 2022

Chromosome 22 Deletions and Suicidal Behavior in Schizophrenia

by Adanty, C., Bani-Fatemi, A., Dai, N., De Luca, V., Gerretsen, P., Graff, A.
Published 2021

A mutation-based gene set predicts survival benefit after immunotherapy across multiple cancers and reveals the immune response landscape

by Bian, J., Chen, P., Lin, Y., Long, J., Sang, X., Wang, A., Wang, D., Yang, X., Zhang, H., Zhao, H., Zheng, M., Zheng, Y.
Published 2022

Genome-scale CRISPR screens identify host factors that promote human coronavirus infection

by Bluhm, A.P, Grodzki, M., Karst, S.M, Norris, M.H, Rafiee, R., Russo, M., Schaefer, M., Sobh, A., Tagmount, A., Vulpe, C.D
Published 2022

Subtype-specific and co-occurring genetic alterations in B-cell non-Hodgkin lymphoma

by Akhter, A., Bhalla, K., Bouska, A., Buckley, S., Carey, C., Chen, B.J, Davidson, M., Davis, R.E, Deng, Q., Fowler, N.H, Gandhi, M., Ghosh, S., Green, M.R, Greiner, T., Hartert, K., Heavican, T., Iqbal, J., Jain, N., Lunning, M.A, Ma, M.C.J, Mansoor, A., Moore, D., Nastoupil, L.J, Neelapu, S., Parekh, S., Perumal, D., Rodig, S.J, Showell, J., Sohani, A.R, Stewart, D., Street, L., Tadros, S., Tobin, J., Vose, J.M, Westin, J.R, Yang, H.
Published 2022

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans

by Bhoj, E.J, Brasch-Andersen, C., Brites, P., Bupp, C., Caluseriu, O., Costa, A.R, Fagerberg, C., Falk, M.J, Feng, I., Ganetzky, R.D, Hakonarson, H., Hansen, L.K, Hill, R.S, Hu, K., Kahle, K.T, Kang, B., Li, D., Muraresku, C.C, Neil, J.E, Pinto-Costa, R., Qi, C., Ruan, X., Sousa, M.M, Walsh, C.A, Zhang, X., Zhong, R.
Published 2022

MCKAT: a multi-dimensional copy number variant kernel association test

by Catchpoole, D., Kennedy, P.J, Khan, J., Maus Esfahani, N.
Published 2021

GSA: an independent development algorithm for calling copy number and detecting homologous recombination deficiency (HRD) from target capture sequencing

by Cai, Y., Chen, D., Li, Q., Meng, P., Shao, M., Shi, T., Song, C., Wang, C., Wang, X.
Published 2021

isoCNV: in silico optimization of copy number variant detection from targeted or exome sequencing data

by Aiese Cigliano, R., Barcelona-Cabeza, R., Sanseverino, W.
Published 2021