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1.

Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26.

Homan, Claire C; Scott, Hamish S; Brown, Anna L.

Blood ; 141(13): 1533-1543, 2023 03 30.

Artículo en Inglés | MEDLINE | ID: mdl-36626254

2.

Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma.

Flerlage, Jamie E; Myers, Jason R; Maciaszek, Jamie L; Oak, Ninad; Rashkin, Sara R; Hui, Yawei; Wang, Yong-Dong; Chen, Wenan; Wu, Gang; Chang, Ti-Cheng; Hamilton, Kayla; Tithi, Saima S; Goldin, Lynn R; Rotunno, Melissa; Caporaso, Neil; Vogt, Aurélie; Flamish, Deborah; Wyatt, Kathleen; Liu, Jia; Tucker, Margaret; Hahn, Christopher N; Brown, Anna L; Scott, Hamish S; Mullighan, Charles; Nichols, Kim E; Metzger, Monika L; McMaster, Mary L; Yang, Jun J; Rampersaud, Evadnie.

Blood ; 141(11): 1293-1307, 2023 03 16.

Artículo en Inglés | MEDLINE | ID: mdl-35977101

3.

Ceramide-induced integrated stress response overcomes Bcl-2 inhibitor resistance in acute myeloid leukemia.

Lewis, Alexander C; Pope, Victoria S; Tea, Melinda N; Li, Manjun; Nwosu, Gus O; Nguyen, Thao M; Wallington-Beddoe, Craig T; Moretti, Paul A B; Anderson, Dovile; Creek, Darren J; Costabile, Maurizio; Ali, Saira R; Thompson-Peach, Chloe A L; Dredge, B Kate; Bert, Andrew G; Goodall, Gregory J; Ekert, Paul G; Brown, Anna L; D'Andrea, Richard; Robinson, Nirmal; Pitman, Melissa R; Thomas, Daniel; Ross, David M; Gliddon, Briony L; Powell, Jason A; Pitson, Stuart M.

Blood ; 139(26): 3737-3751, 2022 06 30.

Artículo en Inglés | MEDLINE | ID: mdl-35443029

4.

Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia.

Duncavage, Eric J; Bagg, Adam; Hasserjian, Robert P; DiNardo, Courtney D; Godley, Lucy A; Iacobucci, Ilaria; Jaiswal, Siddhartha; Malcovati, Luca; Vannucchi, Alessandro M; Patel, Keyur P; Arber, Daniel A; Arcila, Maria E; Bejar, Rafael; Berliner, Nancy; Borowitz, Michael J; Branford, Susan; Brown, Anna L; Cargo, Catherine A; Döhner, Hartmut; Falini, Brunangelo; Garcia-Manero, Guillermo; Haferlach, Torsten; Hellström-Lindberg, Eva; Kim, Annette S; Klco, Jeffery M; Komrokji, Rami; Lee-Cheun Loh, Mignon; Loghavi, Sanam; Mullighan, Charles G; Ogawa, Seishi; Orazi, Attilio; Papaemmanuil, Elli; Reiter, Andreas; Ross, David M; Savona, Michael; Shimamura, Akiko; Skoda, Radek C; Solé, Francesc; Stone, Richard M; Tefferi, Ayalew; Walter, Matthew J; Wu, David; Ebert, Benjamin L; Cazzola, Mario.

Blood ; 140(21): 2228-2247, 2022 11 24.

Artículo en Inglés | MEDLINE | ID: mdl-36130297

5.

Integrating germline variant assessment into routine clinical practice for myelodysplastic syndrome and acute myeloid leukaemia: current strategies and challenges.

Tawana, Kiran; Brown, Anna L; Churpek, Jane E.

Br J Haematol ; 196(6): 1293-1310, 2022 03.

Artículo en Inglés | MEDLINE | ID: mdl-34658019

6.

Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA).

Brown, Anna L; Hahn, Christopher N; Scott, Hamish S.

Blood ; 136(1): 24-35, 2020 07 02.

Artículo en Inglés | MEDLINE | ID: mdl-32430494

7.

GATA2 deficiency syndrome: A decade of discovery.

Homan, Claire C; Venugopal, Parvathy; Arts, Peer; Shahrin, Nur H; Feurstein, Simone; Rawlings, Lesley; Lawrence, David M; Andrews, James; King-Smith, Sarah L; Harvey, Natasha L; Brown, Anna L; Scott, Hamish S; Hahn, Christopher N.

Hum Mutat ; 42(11): 1399-1421, 2021 11.

Artículo en Inglés | MEDLINE | ID: mdl-34387894

8.

Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss.

Venugopal, Parvathy; Gagliardi, Lucia; Forsyth, Cecily; Feng, Jinghua; Phillips, Kerry; Babic, Milena; Poplawski, Nicola K; Rienhoff, Hugh Young; Schreiber, Andreas W; Hahn, Christopher N; Brown, Anna L; Scott, Hamish S.

BMC Med Genet ; 21(1): 35, 2020 02 17.

Artículo en Inglés | MEDLINE | ID: mdl-32066420

9.

And the germline beat (AML) goes on.

Brown, Anna L.

Blood ; 139(8): 1126-1128, 2022 02 24.

Artículo en Inglés | MEDLINE | ID: mdl-35201331

10.

Conditional knockout mice demonstrate function of Klf5 as a myeloid transcription factor.

Shahrin, Nur Hezrin; Diakiw, Sonya; Dent, Lindsay A; Brown, Anna L; D'Andrea, Richard J.

Blood ; 128(1): 55-9, 2016 07 07.

Artículo en Inglés | MEDLINE | ID: mdl-27207790

11.

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.

Lewinsohn, Maya; Brown, Anna L; Weinel, Luke M; Phung, Connie; Rafidi, George; Lee, Ming K; Schreiber, Andreas W; Feng, Jinghua; Babic, Milena; Chong, Chan-Eng; Lee, Young; Yong, Agnes; Suthers, Graeme K; Poplawski, Nicola; Altree, Meryl; Phillips, Kerry; Jaensch, Louise; Fine, Miriam; D'Andrea, Richard J; Lewis, Ian D; Medeiros, Bruno C; Pollyea, Daniel A; King, Mary-Claire; Walsh, Tom; Keel, Siobán; Shimamura, Akiko; Godley, Lucy A; Hahn, Christopher N; Churpek, Jane E; Scott, Hamish S.

Blood ; 127(8): 1017-23, 2016 Feb 25.

Artículo en Inglés | MEDLINE | ID: mdl-26712909

12.

Childhood acute myeloid leukemia shows a high level of germline predisposition.

Samaraweera, Saumya E; Wang, Paul P S; Li, Ka Leung; Casolari, Debora A; Feng, Jinghua; Pinese, Mark; Maung, Kyaw Ze Ya; Leo, Paul; Cowley, Mark; Perkins, Kelly; Smith, Amanda M; Ellis, Jonathan; Wee, Amilia; Hiwase, Devendra K; Scott, Hamish S; Schreiber, Andreas W; Brown, Anna L; Deans, Andrew J; Ross, David M; Moore, Andrew S; Gonda, Thomas J; Hahn, Christopher N; D'Andrea, Richard J.

Blood ; 138(22): 2293-2298, 2021 12 02.

Artículo en Inglés | MEDLINE | ID: mdl-34521114

13.

The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy.

Homan, Claire C; King-Smith, Sarah L; Lawrence, David M; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W; Yu, Kai; Bödör, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; DiNardo, Courtney D; Duployez, Nicolas; Favier, Remi; Fröhling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M; Krämer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A; Schreiber, Andreas W; Hahn, Christopher N; Scott, Hamish S; Brown, Anna L.

Haematologica ; 106(11): 3004-3007, 2021 11 01.

Artículo en Inglés | MEDLINE | ID: mdl-34233450

14.

A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability.

Fox, Lucy C; Tan, Michelle; Brown, Anna L; Arts, Peer; Thompson, Ella; Ryland, Georgina L; Lickiss, Jennifer; Scott, Hamish S; Poplawski, Nicola K; Phillips, Kerry; Came, Neil A; James, Paul; Ting, Stephen B; Ritchie, David S; Szer, Jeff; Hahn, Christopher N; Schwarer, Anthony; Blombery, Piers.

Br J Haematol ; 190(5): e297-e301, 2020 09.

Artículo en Inglés | MEDLINE | ID: mdl-32488879

15.

A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia.

Cheah, Jesse J C; Brown, Anna L; Schreiber, Andreas W; Feng, Jinghua; Babic, Milena; Moore, Sarah; Young, Chun-Chun; Fine, Miriam; Phillips, Kerry; Guandalini, Michael; Wilson, Peter; Poplawski, Nicola; Hahn, Christopher N; Scott, Hamish S.

Haematologica ; 104(7): e318-e321, 2019 07.

Artículo en Inglés | MEDLINE | ID: mdl-30923096

16.

An optimized algorithm for detecting and annotating regional differential methylation.

Li, Sheng; Garrett-Bakelman, Francine E; Akalin, Altuna; Zumbo, Paul; Levine, Ross; To, Bik L; Lewis, Ian D; Brown, Anna L; D'Andrea, Richard J; Melnick, Ari; Mason, Christopher E.

BMC Bioinformatics ; 14 Suppl 5: S10, 2013.

Artículo en Inglés | MEDLINE | ID: mdl-23735126

17.

The double life of KLF5: Opposing roles in regulation of gene-expression, cellular function, and transformation.

Diakiw, Sonya M; D'Andrea, Richard J; Brown, Anna L.

IUBMB Life ; 65(12): 999-1011, 2013 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-24323942

18.

The GM-CSF receptor utilizes ß-catenin and Tcf4 to specify macrophage lineage differentiation.

Brown, Anna L; Salerno, Diana G; Sadras, Teresa; Engler, Grant A; Kok, Chung H; Wilkinson, Christopher R; Samaraweera, Saumya E; Sadlon, Timothy J; Perugini, Michelle; Lewis, Ian D; Gonda, Thomas J; D'Andrea, Richard J.

Differentiation ; 83(1): 47-59, 2012 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-22099176

19.

Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy.

Zerella, Jiarna R; Homan, Claire C; Arts, Peer; Brown, Anna L; Scott, Hamish S; Hahn, Christopher N.

Front Oncol ; 13: 1183318, 2023.

Artículo en Inglés | MEDLINE | ID: mdl-37377909

20.

Novel modes of MPL activation in triple-negative myeloproliferative neoplasms.

Samaraweera, Saumya E; Geukens, Tatjana; Casolari, Debora A; Nguyen, Tran; Sun, Caitlyn; Bailey, Sheree; Moore, Sarah; Feng, Jinghua; Schreiber, Andreas W; Parker, Wendy T; Brown, Anna L; Butcher, Carolyn; Bardy, Peter G; Osborn, Michael; Scott, Hamish S; Talaulikar, Dipti; Grove, Carolyn S; Hahn, Christopher N; D'Andrea, Richard J; Ross, David M.

Pathology ; 55(1): 77-85, 2023 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-36031433

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