Search Results - Andrew Farrell

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  1. 1

    Feeling Seen: Aboriginal and Torres Strait Islander LGBTIQ+ Peoples, (In)Visibility, and Social-Media Assemblages by Andrew Farrell

    Published in Genealogy (2021-06-01)
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  2. 2

    Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias by Eric L. Bogenschutz, Zac D. Fox, Andrew Farrell, Julia Wynn, Barry Moore, Lan Yu, Gudrun Aspelund, Gabor Marth, Mark Yandell, Yufeng Shen, Wendy K. Chung, Gabrielle Kardon

    Published in HGG Advances (2020-10-01)
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  3. 3

    Forward genetic screening identifies a small molecule that blocks Toxoplasma gondii growth by inhibiting both host- and parasite-encoded kinases. by Kevin M Brown, Elena Suvorova, Andrew Farrell, Aaron McLain, Ashley Dittmar, Graham B Wiley, Gabor Marth, Patrick M Gaffney, Marc Jan Gubbels, Michael White, Ira J Blader

    Published in PLoS Pathogens (2014-06-01)
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  4. 4

    Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsies by Xiaomeng Huang, Yi Qiao, Samuel W. Brady, Rachel E. Factor, Erinn Downs-Kelly, Andrew Farrell, Jasmine A. McQuerry, Gajendra Shrestha, David Jenkins, W. Evan Johnson, Adam L. Cohen, Andrea H. Bild, Gabor T. Marth

    Published in Genome Medicine (2021-10-01)
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  5. 5

    P585: Rapid genome sequencing identifies a de novo SNAP25 variant for neonatal congenital myasthenic syndrome by Ting Wen, Hayley Reynolds, Andrew Farrell, Barry Moore, Steven Boyden, Thomas Nicholas, Shawn Rynearson, Carson Holt, Christine Miller, Katherine Noble, Dawn Bentley, Rachel Palmquist, Betsy Ostrander, Stephanie Manberg, Joshua Bonkowsky, Brian Shayota, Sabrina Malone-Jenkins, Pinar Bayrak-Toydemir, Rong Mao

    Published in Genetics in Medicine Open (2023-01-01)
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  6. 6

    P665: Recommendations for the improvement of diagnostic yields in rare disease cases through the integration of structural variants into analytical pipelines by Thomas Nicholas, Andrew Farrell, Shawn Rynearson, Carson Holt, Steven Boyden, Barry Moore, Najla Al-Sweel, Christine Miller, Lucilla Pizzo, Chelsea Solorzano, Rachel Palmquist, Ashley Andrews, Rong Mao, Pinar Bayrak-Toydemir, Eric Fredrickson, Katherine Noble, Brian Shayota, Joshua Bonkowsky, John Carey, Sabrina Malone-Jenkins, Lorenzo Botto, Aaron Quinlan

    Published in Genetics in Medicine Open (2023-01-01)
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  7. 7

    Goanna Walking: A Rubric to Measure Transformation in Critical Indigenous Studies Students by Madi Day, Percy Lezard, Min Kaur, Tamika Worrell, Dylan Barnes, Jo Rey, Ash Moorehead, Zac Roberts, Innez Haua, Tetei Bakic, Andrew Farrell, Michelle Bishop, Sandy O'Sullivan, Bronwyn Carlson, Yanti Ropeyarn, Dakota Jericho Smith, Tyrell Kāmira Sams, Lauren Tynan, Cecilia Marek, Lou Netana-Glover, Nicholet A Deschine Parkhurst, Souksavanh T. Keovorabouth

    Published in Journal of Global Indigeneity (2025-09-01)
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  8. 8

    Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia by Thomas J. Nicholas, Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pinar Bayrak‐Toydemir, Christine E. Miller, Dawn Bentley, Rachel Palmquist, Barry Moore, Edgar J. Hernandez, Michael J. Cormier, Eric Fredrickson, Katherine Noble, Shawn Rynearson, Carson Holt, Mary Anne Karren, Joshua L. Bonkowsky, Martin Tristani‐Firouzi, Mark Yandell, Gabor Marth, Aaron R. Quinlan, Luca Brunelli, Reha M. Toydemir, Brian J. Shayota, John C. Carey, Steven E. Boyden, Sabrina Malone Jenkins

    Published in Molecular Genetics & Genomic Medicine (2022-04-01)
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  9. 9

    P516: RNASeq analysis identifies the pathogenicity of inherited synonymous splice-region variant in NEB, confirming a diagnosis of neonatal nemaline myopathy 2 by Barry Moore, Thomas Nicholas, Rong Mao, Brian Shayota, Steven Boyden, Chelsea Solorzano, Rachel Palmquist, Pinar Bayrak-Toydemir, Katherine Noble, Andrew Farrell, Edgar Hernandez, Shawn Rynearson, Carson Holt, Alistair Ward, Eric Fredrickson, Kelsey Nicholson, David Pattison, Jian Zhao, Makenzie Fulmer, Lucilla Pizzo, Ting Wen, John O'Shea, Robert Lewis, Hayley Reynolds, Betsy Ostrander, Hunter Best, Luca Brunelli, Mark Yandell, Gabor Marth, Aaron Quinlan, John Carey, Martin Tristani-Firouzi, Joshua Bonkowsky, Sabrina Malone-Jenkins

    Published in Genetics in Medicine Open (2023-01-01)
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  10. 10

    P243: The Utah NeoSeq Project: Developing and implementing genomic sequencing in acute neonatal care by Sabrina Malone-Jenkins, Brian Shayota, Chelsea Solorzano, Rachel Palmquist, Steven Boyden, Barry Moore, Thomas Nicholas, Rong Mao, Pinar Bayrak-Toydemir, Katherine Noble, Andrew Farrell, Edgar Hernandez, Shawn Rynearson, Carson Holt, Alistair Ward, Najla Al-Sweel, Jian Zhao, Makenzie Fulmer, Lucilla Pizzo, Ting Wen, John O'Shea, Robert Lewis, Hayley Reynolds, Eric Fredrickson, Kelsey Nicholson, David Pattison, Hunter Best, Luca Brunelli, Mark Yandell, Gabor Marth, Aaron Quinlan, John Carey, Martin Tristani-Firouzi, Joshua Bonkowsky

    Published in Genetics in Medicine Open (2023-01-01)
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  11. 11

    Envisioning Aboriginal and Torres Strait Islander AI Futures Communique: March 2025 by Rose Barrowcliffe, Ben Hutchinson, Angie Abdilla, Lesley Acres, Bianca Beetson, Aaron Bell, Penelope Benton, Becky Bligh, Robert Bowen, Nichola Burton, Bronwyn Carlson, Renee Cawthorne, Andrew Hammond, Innez Haua, Courtney Henry, Bernadette Hyland-Wood, Rebecca Lyons, Robert McLellan, Georgia Mokak, Levi Murray, Lotus Rana, Cassandra Sedran-Price, Peter Sefton, Ryan Stoker, Narissa Timbery, Danilo Urzedo, Phoebe Weston-Evans, Tamika Worrell, Shevaun Wright, Becki Cook, Andrew Farrell, Dennis Fay, John Fejo, Jenny Fewster, Neenah Gray, David Hackman

    Published in Journal of Global Indigeneity (2025-03-01)
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  12. 12

    BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistance by Ksenija Nesic, John J. Krais, Yifan Wang, Cassandra J. Vandenberg, Pooja Patel, Kathy Q. Cai, Tanya Kwan, Elizabeth Lieschke, Gwo-Yaw Ho, Holly E. Barker, Justin Bedo, Silvia Casadei, Andrew Farrell, Marc Radke, Kristy Shield-Artin, Jocelyn S. Penington, Franziska Geissler, Elizabeth Kyran, Robert Betsch, Lijun Xu, Fan Zhang, Alexander Dobrovic, Inger Olesen, Rebecca Kristeleit, Amit Oza, Iain McNeish, Gayanie Ratnayake, Nadia Traficante, Australian Ovarian Cancer Study, Anna DeFazio, David D. L. Bowtell, Thomas C. Harding, Kevin Lin, Elizabeth M. Swisher, Olga Kondrashova, Clare L. Scott, Neil Johnson, Matthew J. Wakefield

    Published in Molecular Cancer (2024-08-01)
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