Mutations in the PCNA-binding site of CDKN1C inhibit cell proliferation by impairing the entry into S phase

por Borges, Kleiton S, Arboleda, Valerie A, Vilain, Eric
Publicado 2015

DMRscaler: a scale-aware method to identify regions of differential DNA methylation spanning basepair to multi-megabase features

por Bondhus, Leroy, Wei, Angela, Arboleda, Valerie A.
Publicado 2022

Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificity

por Bondhus, Leroy, Varma, Roshni, Hernandez, Yenifer, Arboleda, Valerie A
Publicado 2022

From chemoproteomic‐detected amino acids to genomic coordinates: insights into precise multi‐omic data integration

por Palafox, Maria F, Desai, Heta S, Arboleda, Valerie A, Backus, Keriann M
Publicado 2021

Lean Principles to Improve Quality in High-Throughput COVID-19 Testing Using SwabSeq: A Barcoded Sequencing-Based Testing Platform

por Jones, Janae, Saul, Rosita, Sathe, Laila, Xie, Joanna, Marquette, Dawn, Arboleda, Valerie A
Publicado 2021

Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease

por Spendlove, Sarah J., Bondhus, Leroy, Lluri, Gentian, Sul, Jae Hoon, Arboleda, Valerie A.
Publicado 2022

Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation

por Lin, Isabella, Wei, Angela, Awamleh, Zain, Singh, Meghna, Ning, Aileen, Herrera, Analeyla, Russell, Bianca E., Weksberg, Rosanna, Arboleda, Valerie A.
Publicado 2023

Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells

por Bramble, Matthew S., Roach, Lara, Lipson, Allen, Vashist, Neerja, Eskin, Ascia, Ngun, Tuck, Gosschalk, Jason E., Klein, Steven, Barseghyan, Hayk, Arboleda, Valerie A., Vilain, Eric
Publicado 2016

MicroRNA-146a modulates B-cell oncogenesis by regulating Egr1

por Contreras, Jorge R., Palanichamy, Jayanth Kumar, Tran, Tiffany M., Fernando, Thilini R., Rodriguez-Malave, Norma I., Goswami, Neha, Arboleda, Valerie A., Casero, David, Rao, Dinesh S.
Publicado 2015

Lower Severe Acute Respiratory Syndrome Coronavirus 2 Viral Shedding Following Coronavirus Disease 2019 Vaccination Among Healthcare Workers in Los Angeles, California

por Adamson, Paul C, Pfeffer, Michael A, Arboleda, Valerie A, Garner, Omai B, de St Maurice, Annabelle, von Bredow, Benjamin, Flint, Jonathan, Kruglyak, Leonid, Currier, Judith S
Publicado 2021

KAT6A mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior HOXC cluster

por Singh, Meghna, Spendlove, Sarah, Wei, Angela, Bondhus, Leroy, Nava, Aileen, de L. Vitorino, Francisca N., Amano, Seth, Lee, Jacob, Echeverria, Gesenia, Gomez, Dianne, Garcia, Benjamin A., Arboleda, Valerie A.
Publicado 2023

Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y(POS) mouse model

por Barseghyan, Hayk, Symon, Aleisha, Zadikyan, Mariam, Almalvez, Miguel, Segura, Eva E., Eskin, Ascia, Bramble, Matthew S., Arboleda, Valerie A., Baxter, Ruth, Nelson, Stanley F., Délot, Emmanuèle C., Harley, Vincent, Vilain, Eric
Publicado 2018

KAT6A mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior HOXC cluster

por Singh, Meghna, Spendlove, Sarah J., Wei, Angela, Bondhus, Leroy M., Nava, Aileen A., de L. Vitorino, Francisca N., Amano, Seth, Lee, Jacob, Echeverria, Gesenia, Gomez, Dianne, Garcia, Benjamin A., Arboleda, Valerie A.
Publicado 2023

DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

por Awamleh, Zain, Chater-Diehl, Eric, Choufani, Sanaa, Wei, Elizabeth, Kianmahd, Rebecca R., Yu, Anna, Chad, Lauren, Costain, Gregory, Tan, Wen-Hann, Scherer, Stephen W., Arboleda, Valerie A., Russell, Bianca E., Weksberg, Rosanna
Publicado 2022

Genomic epidemiology of the Los Angeles COVID-19 outbreak and the early history of the B.1.43 strain in the USA

por Guo, Longhua, Boocock, James, Hilt, Evann E., Chandrasekaran, Sukantha, Zhang, Yi, Munugala, Chetan, Sathe, Laila, Alexander, Noah, Arboleda, Valerie A., Flint, Jonathan, Eskin, Eleazar, Luo, Chongyuan, Yang, Shangxin, Garner, Omai B., Yin, Yi, Bloom, Joshua S., Kruglyak, Leonid
Publicado 2022

Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy

por Sono, Reiri, Larrinaga, Tania M., Huang, Alden, Makhlouf, Frank, Kang, Xuedong, Su, Jonathan, Lau, Ryan, Arboleda, Valerie A., Biniwale, Reshma, Fishbein, Gregory A., Khanlou, Negar, Si, Ming-Sing, Satou, Gary M., Halnon, Nancy, Van Arsdell, Glen S., Gregorio, Carol C., Nelson, Stanly, Touma, Marlin
Publicado 2023

Mutations in the PCNA-binding domain of CDKN1C cause IMAGE Syndrome

por Arboleda, Valerie A., Lee, Hane, Parnaik, Rahul, Fleming, Alice, Banerjee, Abhik, Ferraz-de-Souza, Bruno, Délot, Emmanuèle C., Rodriguez-Fernandez, Imilce A., Braslavsky, Debora, Bergadá, Ignacio, Dell’Angelica, Esteban C., Nelson, Stanley F., Martinez-Agosto, Julian A., Achermann, John C., Vilain, Eric
Publicado 2012

Metabolic reprogramming and epigenetic changes of vital organs in SARS-CoV-2–induced systemic toxicity

por Li, Shen, Ma, Feiyang, Yokota, Tomohiro, Garcia, Gustavo, Palermo, Amelia, Wang, Yijie, Farrell, Colin, Wang, Yu-Chen, Wu, Rimao, Zhou, Zhiqiang, Pan, Calvin, Morselli, Marco, Teitell, Michael A., Ryazantsev, Sergey, Fishbein, Gregory A., Hoeve, Johanna ten, Arboleda, Valerie A., Bloom, Joshua, Dillon, Barbara, Pellegrini, Matteo, Lusis, Aldons J., Graeber, Thomas G., Arumugaswami, Vaithilingaraja, Deb, Arjun
Publicado 2021

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

por Johnson, Ruth, Ding, Yi, Venkateswaran, Vidhya, Bhattacharya, Arjun, Boulier, Kristin, Chiu, Alec, Knyazev, Sergey, Schwarz, Tommer, Freund, Malika, Zhan, Lingyu, Burch, Kathryn S., Caggiano, Christa, Hill, Brian, Rakocz, Nadav, Balliu, Brunilda, Denny, Christopher T., Sul, Jae Hoon, Zaitlen, Noah, Arboleda, Valerie A., Halperin, Eran, Sankararaman, Sriram, Butte, Manish J., Lajonchere, Clara, Geschwind, Daniel H., Pasaniuc, Bogdan
Publicado 2022

Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

por Johnson, Ruth, Ding, Yi, Venkateswaran, Vidhya, Bhattacharya, Arjun, Boulier, Kristin, Chiu, Alec, Knyazev, Sergey, Schwarz, Tommer, Freund, Malika, Zhan, Lingyu, Burch, Kathryn S., Caggiano, Christa, Hill, Brian, Rakocz, Nadav, Balliu, Brunilda, Denny, Christopher T., Sul, Jae Hoon, Zaitlen, Noah, Arboleda, Valerie A., Halperin, Eran, Sankararaman, Sriram, Butte, Manish J., Lajonchere, Clara, Geschwind, Daniel H., Pasaniuc, Bogdan
Publicado 2022