Blanche P Alter

Publication Activity (10 Years)

Years Active: 2016-2022
Publications (10 Years): 11

Top Topics

Mesenchymal Stem Cells

Machine Learning

Intellectual Disability

Top Venues

British journal of haematology

The EMBO journal

Science advances

This page only lists publications with an associated author ORCID identifier.

Publications

Fernanda Gutierrez-Rodrigues, Eric Munger, Xiaoyang Ma, Emma M Groarke, Youbao Tang, Bhavisha A Patel, Luis Fernando B Catto, Diego Villa Clé, Marena R Niewisch, Raquel Ma Paiva, Flavia Donaires, André Luiz Pinto, Gustavo Borges, Barbara A Santana, Lisa J McReynolds, Neelam Giri, Burak Altintas, Xing Fan, Ruba N Shalhoub, Christopher Mark Siwy, Carrie Diamond, Diego Quinones Raffo, Kathleen Marie Craft, Sachiko Kajigaya, Ronald M Summers, Paul P Liu, Lea Cunningham, Dennis D Hickstein, Cynthia E Dunbar, Ricardo Pasquini, Michel Michels de Oliveira, Elvira Deolinda Rodrigues Pereira Velloso, Blanche P Alter, Sharon A Savage, Carmem Maria Sales Bonfim, Colin O Wu, Rodrigo do Tocantins Calado, Neal S Young
Differential diagnosis of bone marrow failure syndromes guided by machine learning. Blood (2022)
Fernanda Gutierrez-Rodrigues, Eric Munger, Xiaoyang Ma, Emma M Groarke, Youbao Tang, Bhavisha A Patel, Luis Fernando B Catto, Diego Villa Clé, Marena R Niewisch, Raquel Ma Paiva, Flavia Donaires, André Luiz Pinto, Gustavo Borges, Barbara A Santana, Lisa J McReynolds, Neelam Giri, Burak Altintas, Xing Fan, Ruba N Shalhoub, Christopher Mark Siwy, Carrie Diamond, Diego Quinones Raffo, Kathleen Marie Craft, Sachiko Kajigaya, Ronald M Summers, Paul P Liu, Lea Cunningham, Dennis D Hickstein, Cynthia E Dunbar, Ricardo Pasquini, Michel Michels de Oliveira, Elvira Deolinda Rodrigues Pereira Velloso, Blanche P Alter, Sharon A Savage, Carmem Maria Sales Bonfim, Colin O Wu, Rodrigo do Tocantins Calado, Neal S Young
Differential diagnosis of bone marrow failure syndromes guided by machine learning. Blood (2022)
Blanche P Alter, Neelam Giri, Lisa J McReynolds, Burak Altintas
Fanconi anaemia: A syndrome with distinct subgroups. British journal of haematology 197 (4) (2022)
Marena R Niewisch, Neelam Giri, Lisa J McReynolds, Rotana Alsaggaf, Sonia Bhala, Blanche P Alter, Sharon A Savage
Disease Progression and Clinical Outcomes in Telomere Biology Disorders. Blood (2021)
Alison M Taylor, Elizabeth R Macari, Iris T Chan, Megan C Blair, Sergei Doulatov, Linda T Vo, David M Raiser, Kavitha Siva, Anindita Basak, Mehdi Pirouz, Arish N Shah, Katherine McGrath, Jessica M Humphries, Emma Stillman, Blanche P Alter, Eliezer Calo, Richard I Gregory, Vijay G Sankaran, Johan Flygare, Benjamin L Ebert, Yi Zhou, George Q Daley, Leonard I Zon
Calmodulin inhibitors improve erythropoiesis in Diamond-Blackfan anemia. Science translational medicine 12 (566) (2021)
Neelam Giri, Blanche P Alter, Sharon A Savage, Pamela Stratton
Gynaecological and reproductive health of women with telomere biology disorders. British journal of haematology 193 (6) (2021)
Chongkui Sun, Kun Wang, Amanda J Stock, Yi Gong, Tyler G Demarest, Beimeng Yang, Neelam Giri, Lea Harrington, Blanche P Alter, Sharon A Savage, Vilhelm A Bohr, Yie Liu
Re-equilibration of imbalanced NAD metabolism ameliorates the impact of telomere dysfunction. The EMBO journal 39 (21) (2020)
Eléonore Toufektchan, Vincent Lejour, Romane Durand, Neelam Giri, Irena Draskovic, Boris Bardot, Pierre Laplante, Sara Jaber, Blanche P Alter, José-Arturo Londono-Vallejo, Sharon A Savage, Franck Toledo
Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance. Science advances 6 (15) (2020)
Blanche P Alter, Neelam Giri
Serum alpha fetoprotein levels in Fanconi anaemia. British journal of haematology 184 (6) (2018)
Neelam Giri, Pamela Stratton, Sharon A Savage, Blanche P Alter
Pregnancies in patients with inherited bone marrow failure syndromes in the NCI cohort. Blood 130 (14) (2017)
Jennifer T Loud, Renee C Bremer, Phuong L Mai, June A Peters, Neelam Giri, Douglas R Stewart, Mark H Greene, Blanche P Alter, Sharon A Savage
Research participant interest in primary, secondary, and incidental genomic findings. Genetics in medicine : official journal of the American College of Medical Genetics 18 (12) (2016)