Somatic Mutation, Genomic Variation, and Neurological Disease
Poduri, Annapurna, Evrony, Gilad D., Cai, Xuyu, Walsh, Christopher A.
Published in Science (American Association for the Advancement of Science) (05.07.2013)
Published in Science (American Association for the Advancement of Science) (05.07.2013)
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Journal Article
Applications of Single-Cell DNA Sequencing
Evrony, Gilad D, Hinch, Anjali Gupta, Luo, Chongyuan
Published in Annual review of genomics and human genetics (31.08.2021)
Published in Annual review of genomics and human genetics (31.08.2021)
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Journal Article
Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain
Evrony, Gilad D., Cai, Xuyu, Lee, Eunjung, Hills, L. Benjamin, Elhosary, Princess C., Lehmann, Hillel S., Parker, J.J., Atabay, Kutay D., Gilmore, Edward C., Poduri, Annapurna, Park, Peter J., Walsh, Christopher A.
Published in Cell (26.10.2012)
Published in Cell (26.10.2012)
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Journal Article
Somatic mutation in single human neurons tracks developmental and transcriptional history
Lodato, Michael A., Woodworth, Mollie B., Lee, Semin, Evrony, Gilad D., Mehta, Bhaven K., Karger, Amir, Lee, Soohyun, Chittenden, Thomas W., D'Gama, Alissa M., Cai, Xuyu, Luquette, Lovelace J., Lee, Eunjung, Park, Peter J., Walsh, Christopher A.
Published in Science (American Association for the Advancement of Science) (02.10.2015)
Published in Science (American Association for the Advancement of Science) (02.10.2015)
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Journal Article
Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain
Cai, Xuyu, Evrony, Gilad D., Lehmann, Hillel S., Elhosary, Princess C., Mehta, Bhaven K., Poduri, Annapurna, Walsh, Christopher A.
Published in Cell reports (Cambridge) (11.09.2014)
Published in Cell reports (Cambridge) (11.09.2014)
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Journal Article
Cell lineage analysis in human brain using endogenous retroelements
Evrony, Gilad D, Lee, Eunjung, Mehta, Bhaven K, Benjamini, Yuval, Johnson, Robert M, Cai, Xuyu, Yang, Lixing, Haseley, Psalm, Lehmann, Hillel S, Park, Peter J, Walsh, Christopher A
Published in Neuron (Cambridge, Mass.) (07.01.2015)
Published in Neuron (Cambridge, Mass.) (07.01.2015)
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Journal Article
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
Poduri, Annapurna, Evrony, Gilad D., Cai, Xuyu, Elhosary, Princess Christina, Beroukhim, Rameen, Lehtinen, Maria K., Hills, L. Benjamin, Heinzen, Erin L., Hill, Anthony, Hill, R. Sean, Barry, Brenda J., Bourgeois, Blaise F.D., Riviello, James J., Barkovich, A. James, Black, Peter M., Ligon, Keith L., Walsh, Christopher A.
Published in Neuron (Cambridge, Mass.) (12.04.2012)
Published in Neuron (Cambridge, Mass.) (12.04.2012)
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Journal Article
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity
Bae, Jin H., Liu, Ruolin, Roberts, Eugenia, Nguyen, Erica, Tabrizi, Shervin, Rhoades, Justin, Blewett, Timothy, Xiong, Kan, Gydush, Gregory, Shea, Douglas, An, Zhenyi, Patel, Sahil, Cheng, Ju, Sridhar, Sainetra, Liu, Mei Hong, Lassen, Emilie, Skytte, Anne-Bine, Grońska-Pęski, Marta, Shoag, Jonathan E., Evrony, Gilad D., Parsons, Heather A., Mayer, Erica L., Makrigiorgos, G. Mike, Golub, Todd R., Adalsteinsson, Viktor A.
Published in Nature genetics (01.05.2023)
Published in Nature genetics (01.05.2023)
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Journal Article
Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation
Yang, Yawei J., Baltus, Andrew E., Mathew, Rebecca S., Murphy, Elisabeth A., Evrony, Gilad D., Gonzalez, Dilenny M., Wang, Estee P., Marshall-Walker, Christine A., Barry, Brenda J., Murn, Jernej, Tatarakis, Antonis, Mahajan, Muktar A., Samuels, Herbert H., Shi, Yang, Golden, Jeffrey A., Mahajnah, Muhammad, Shenhav, Ruthie, Walsh, Christopher A.
Published in Cell (21.11.2012)
Published in Cell (21.11.2012)
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Journal Article
Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome
Evrony, Gilad D, Cordero, Dwight R, Shen, Jun, Partlow, Jennifer N, Yu, Timothy W, Rodin, Rachel E, Hill, R Sean, Coulter, Michael E, Lam, Anh-Thu N, Jayaraman, Divya, Gerrelli, Dianne, Diaz, Diana G, Santos, Chloe, Morrison, Victoria, Galli, Antonella, Tschulena, Ulrich, Wiemann, Stefan, Martel, M Jocelyne, Spooner, Betty, Ryu, Steven C, Elhosary, Princess C, Richardson, Jillian M, Tierney, Danielle, Robinson, Christopher A, Chibbar, Rajni, Diudea, Dana, Folkerth, Rebecca, Wiebe, Sheldon, Barkovich, A James, Mochida, Ganeshwaran H, Irvine, James, Lemire, Edmond G, Blakley, Patricia, Walsh, Christopher A
Published in Genome research (01.08.2017)
Published in Genome research (01.08.2017)
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Journal Article
Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis
Chorin, Odelia, Yachelevich, Naomi, Mohamed, Khaled, Moscatelli, Ilana, Pappas, John, Henriksen, Kim, Evrony, Gilad D.
Published in Molecular genetics & genomic medicine (01.10.2020)
Published in Molecular genetics & genomic medicine (01.10.2020)
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Journal Article
Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons
Townsend, Seth A, Evrony, Gilad D, Gu, Frank X, Schulz, Martin P, Brown, Robert H, Langer, Robert
Published in Biomaterials (01.12.2007)
Published in Biomaterials (01.12.2007)
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Journal Article
METTL23, a transcriptional partner of GABPA, is essential for human cognition
Reiff, Rachel E, Ali, Bassam R, Baron, Byron, Yu, Timothy W, Ben-Salem, Salma, Coulter, Michael E, Schubert, Christian R, Hill, R Sean, Akawi, Nadia A, Al-Younes, Banan, Kaya, Namik, Evrony, Gilad D, Al-Saffar, Muna, Felie, Jillian M, Partlow, Jennifer N, Sunu, Christine M, Schembri-Wismayer, Pierre, Alkuraya, Fowzan S, Meyer, Brian F, Walsh, Christopher A, Al-Gazali, Lihadh, Mochida, Ganeshwaran H
Published in Human molecular genetics (01.07.2014)
Published in Human molecular genetics (01.07.2014)
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Journal Article
One brain, many genomes
Evrony, Gilad D.
Published in Science (American Association for the Advancement of Science) (04.11.2016)
Published in Science (American Association for the Advancement of Science) (04.11.2016)
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Journal Article
High-fidelity, large-scale targeted profiling of microsatellites
Loh, Caitlin A, Shields, Danielle A, Schwing, Adam, Evrony, Gilad D
Published in Genome research (01.07.2024)
Published in Genome research (01.07.2024)
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Journal Article
Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain
Cai, Xuyu, Evrony, Gilad D., Lehmann, Hillel S., Elhosary, Princess C., Mehta, Bhaven K., Poduri, Annapurna, Walsh, Christopher A.
Published in Cell reports (Cambridge) (03.02.2015)
Published in Cell reports (Cambridge) (03.02.2015)
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Journal Article
Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome
Rizvi, Midhat, Truong, Tina K, Zhou, Janet, Batta, Manav, Moran, Ellen S, Pappas, John, Chu, Mary Lynn, Caluseriu, Oana, Evrony, Gilad D, Leslie, Elaine M, Cordat, Emmanuelle
Published in Human molecular genetics (20.04.2023)
Published in Human molecular genetics (20.04.2023)
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Journal Article
Serial enrichment of heteroduplex DNA using a MutS-magnetic bead system
Murphy, Zachary R, Shields, Danielle A, Evrony, Gilad D
Published in Biotechnology journal (01.01.2023)
Published in Biotechnology journal (01.01.2023)
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