Rapid Flow Cytometry–Based Structural Maintenance of Chromosomes 1 (SMC1) Phosphorylation Assay for Identification of Ataxia-Telangiectasia Homozygotes and Heterozygotes

অনুযায়ী Nahas, Shareef A., Butch, Anthony W., Du, Liutao, Gatti, Richard A.
প্রকাশিত 2009

Assessing ‘Radiosensitivity’ with kinetic profiles of γ-H2AX, 53BP1 and BRCA1 Foci

অনুযায়ী Martin, Nathan T., Nahas, Shareef A., Tunuguntla, Rashmi, Fike, Francesca, Gatti, Richard A.
প্রকাশিত 2011

Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome

অনুযায়ী Farnaes, Lauge, Nahas, Shareef A., Chowdhury, Shimul, Nelson, James, Batalov, Serge, Dimmock, David M., Kingsmore, Stephen F.
প্রকাশিত Cold Spring Harb Mol Case Stud (2017)

ATM–Dependent MiR-335 Targets CtIP and Modulates the DNA Damage Response

অনুযায়ী Martin, Nathan T., Nakamura, Kotoka, Davies, Robert, Nahas, Shareef A., Brown, Christina, Tunuguntla, Rashmi, Gatti, Richard A., Hu, Hailiang
প্রকাশিত 2013

Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons

অনুযায়ী Lai, Chih-Hung, Chun, Helen H., Nahas, Shareef A., Mitui, Midori, Gamo, Kristin M., Du, Liutao, Gatti, Richard A.
প্রকাশিত 2004

Comprehensive Profiling of Radiosensitive Human Cell Lines with DNA Damage Response Assays Identifies the Neutral Comet Assay as a Potential Surrogate for Clonogenic Survival

অনুযায়ী Nahas, Shareef A., Davies, Robert, Fike, Francesca, Nakamura, Kotoka, Du, Liutao, Kayali, Refik, Martin, Nathan T., Concannon, Patrick, Gatti, Richard A.
প্রকাশিত Radiat Res (2011)

The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin–Siris syndrome in an infant with left congenital diaphragm...

অনুযায়ী Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Campo, Miguel Del, Jones, Marilyn C., Dimmock, David P., Kingsmore, Stephen F.
প্রকাশিত Cold Spring Harb Mol Case Stud (2018)

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

অনুযায়ী Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.
প্রকাশিত NPJ Genom Med (2021)

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

অনুযায়ী Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.
প্রকাশিত NPJ Genom Med (2021)

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

অনুযায়ী Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.
প্রকাশিত NPJ Genom Med (2021)

MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significance

অনুযায়ী Kwok, Brian, Hall, Jeff M., Witte, John S., Xu, Yin, Reddy, Prashanti, Lin, Keming, Flamholz, Rachel, Dabbas, Bashar, Yung, Aine, Al-Hafidh, Jenan, Balmert, Emily, Vaupel, Christine, El Hader, Carlos, McGinniss, Matthew J., Nahas, Shareef A., Kines, Julie, Bejar, Rafael
প্রকাশিত Blood (2015)

Rapid whole genome sequencing has clinical utility in children in the pediatric intensive care unit

অনুযায়ী Sanford, Erica F., Clark, Michelle M., Farnaes, Lauge, Williams, Matthew R., Perry, James C., Ingulli, Elizabeth G., Sweeney, Nathaly M., Doshi, Ami, Gold, Jeffrey J., Briggs, Benjamin, Bainbridge, Matthew N., Feddock, Michele, Watkins, Kelly, Chowdhury, Shimul, Nahas, Shareef A., Dimmock, David P., Kingsmore, Stephen F., Coufal, Nicole G.
প্রকাশিত Pediatr Crit Care Med (2019)

Functional precision medicine identifies new therapeutic candidates for medulloblastoma

অনুযায়ী Rusert, Jessica M., Juarez, Edwin F., Brabetz, Sebastian, Jensen, James, Garancher, Alexandra, Chau, Lianne Q., Tacheva-Grigorova, Silvia K., Wahab, Sameerah, Udaka, Yoko T., Finlay, Darren, Seker-Cin, Huriye, Reardon, Brendan, Gröbner, Susanne, Serrano, Jonathan, Ecker, Jonas, Qi, Lin, Kogiso, Mari, Du, Yuchen, Baxter, Patricia A., Henderson, Jacob J., Berens, Michael E., Vuori, Kristiina, Milde, Till, Cho, Yoon-Jae, Li, Xiao-Nan, Olson, James M., Reyes, Iris, Snuderl, Matija, Wong, Terence C., Dimmock, David P., Nahas, Shareef A., Malicki, Denise, Crawford, John R., Levy, Michael L., Van Allen, Eliezer M., Pfister, Stefan M., Tamayo, Pablo, Kool, Marcel, Mesirov, Jill P., Wechsler-Reya, Robert J.
প্রকাশিত Cancer Res (2020)

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis

অনুযায়ী Traspas, Ricardo Moreno, Teoh, Tze Shin, Wong, Pui-Mun, Maier, Michael, Chia, Crystal Y., Lay, Kenneth, Ali, Nur Ain, Larson, Austin, Mutairi, Fuad Al, Al-Sannaa, Nouriya Abbas, Faqeih, Eissa Ali, Alfadhel, Majid, Cheema, Huma Arshad, Dupont, Juliette, Bézieau, Stéphane, Isidor, Bertrand, Yanwen Low, Dorrain, Wang, Yulan, Tan, Grace, Lai, Poh San, Piloquet, Hugues, Joubert, Madeleine, Kayserili, Hulya, Kripps, Kimberly A., Nahas, Shareef A., Wartchow, Eric P., Warren, Mikako, Bhavani, Gandham SriLakshmi, Dasouki, Majed, Sandoval, Renata, Carvalho, Elisa, Ramos, Luiza, Porta, Gilda, Wu, Bin, Lashkari, Harsha Prasada, AlSaleem, Badr, BaAbbad, Raeda M., Abreu Ferrão, Anabela Natália, Karageorgou, Vasiliki, Ordonez-Herrera, Natalia, Khan, Suliman, Bauer, Peter, Cogne, Benjamin, Bertoli-Avella, Aida M., Vincent, Marie, Girisha, Katta Mohan, Reversade, Bruno
প্রকাশিত Nat Genet (2022)