
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes
Yasunobu Nagata, Satoshi Narumi, Yihong Guan, et al.
Blood (2018) Vol. 132, Iss. 21, pp. 2309-2313
Open Access | Times Cited: 52
Yasunobu Nagata, Satoshi Narumi, Yihong Guan, et al.
Blood (2018) Vol. 132, Iss. 21, pp. 2309-2313
Open Access | Times Cited: 52
Showing 1-25 of 52 citing articles:
Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases
Adriana A. de Jesus, Yangfeng Hou, Stephen R. Brooks, et al.
Journal of Clinical Investigation (2019) Vol. 130, Iss. 4, pp. 1669-1682
Open Access | Times Cited: 192
Adriana A. de Jesus, Yangfeng Hou, Stephen R. Brooks, et al.
Journal of Clinical Investigation (2019) Vol. 130, Iss. 4, pp. 1669-1682
Open Access | Times Cited: 192
Advances in germline predisposition to acute leukaemias and myeloid neoplasms
Jeffery M. Klco, Charles G. Mullighan
Nature reviews. Cancer (2020) Vol. 21, Iss. 2, pp. 122-137
Open Access | Times Cited: 124
Jeffery M. Klco, Charles G. Mullighan
Nature reviews. Cancer (2020) Vol. 21, Iss. 2, pp. 122-137
Open Access | Times Cited: 124
Somatic genetic rescue in Mendelian haematopoietic diseases
Patrick Revy, Caroline Kannengiesser, Alain Fischer
Nature Reviews Genetics (2019) Vol. 20, Iss. 10, pp. 582-598
Closed Access | Times Cited: 92
Patrick Revy, Caroline Kannengiesser, Alain Fischer
Nature Reviews Genetics (2019) Vol. 20, Iss. 10, pp. 582-598
Closed Access | Times Cited: 92
Identification and prioritization of myeloid malignancy germline variants in a large cohort of adult patients with AML
Fei Yang, Nicola Long, Tauangtham Anekpuritanang, et al.
Blood (2021) Vol. 139, Iss. 8, pp. 1208-1221
Open Access | Times Cited: 76
Fei Yang, Nicola Long, Tauangtham Anekpuritanang, et al.
Blood (2021) Vol. 139, Iss. 8, pp. 1208-1221
Open Access | Times Cited: 76
Impact of diagnostic genetics on remission MRD and transplantation outcomes in older patients with AML
H. Moses Murdock, Haesook T. Kim, Nathan Denlinger, et al.
Blood (2022) Vol. 139, Iss. 24, pp. 3546-3557
Open Access | Times Cited: 53
H. Moses Murdock, Haesook T. Kim, Nathan Denlinger, et al.
Blood (2022) Vol. 139, Iss. 24, pp. 3546-3557
Open Access | Times Cited: 53
Myelodysplastic syndromes
Huan Li, Fang‐Wen Hu, Robert Peter Gale, et al.
Nature Reviews Disease Primers (2022) Vol. 8, Iss. 1
Closed Access | Times Cited: 48
Huan Li, Fang‐Wen Hu, Robert Peter Gale, et al.
Nature Reviews Disease Primers (2022) Vol. 8, Iss. 1
Closed Access | Times Cited: 48
Inherited Bone Marrow Failure Syndromes
Lorraine E. Canham, Jill L. O. de Jong
Elsevier eBooks (2024), pp. 51-94
Closed Access | Times Cited: 10
Lorraine E. Canham, Jill L. O. de Jong
Elsevier eBooks (2024), pp. 51-94
Closed Access | Times Cited: 10
A Therapeutic Strategy for Preferential Targeting of TET2-Mutant and TET Dioxygenase–Deficient Cells in Myeloid Neoplasms
Yihong Guan, Anand D. Tiwari, James G. Phillips, et al.
Blood Cancer Discovery (2020) Vol. 2, Iss. 2, pp. 146-161
Open Access | Times Cited: 49
Yihong Guan, Anand D. Tiwari, James G. Phillips, et al.
Blood Cancer Discovery (2020) Vol. 2, Iss. 2, pp. 146-161
Open Access | Times Cited: 49
New spinocerebellar ataxia subtype caused bySAMD9Lmutation triggering mitochondrial dysregulation (SCA49)
Marc Corral‐Juan, Pilar Casquero, Natalia Giraldo-Restrepo, et al.
Brain Communications (2022) Vol. 4, Iss. 2
Open Access | Times Cited: 26
Marc Corral‐Juan, Pilar Casquero, Natalia Giraldo-Restrepo, et al.
Brain Communications (2022) Vol. 4, Iss. 2
Open Access | Times Cited: 26
Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity
Elisabetta Molteni, Elisa Bono, Anna Gallì, et al.
Blood (2023) Vol. 142, Iss. 7, pp. 643-657
Open Access | Times Cited: 14
Elisabetta Molteni, Elisa Bono, Anna Gallì, et al.
Blood (2023) Vol. 142, Iss. 7, pp. 643-657
Open Access | Times Cited: 14
Insights into the Molecular Mechanisms of Genetic Predisposition to Hematopoietic Malignancies: The Importance of Gene–Environment Interactions
César Cobaleda, Lucy A. Godley, Kim E. Nichols, et al.
Cancer Discovery (2024) Vol. 14, Iss. 3, pp. 396-405
Open Access | Times Cited: 5
César Cobaleda, Lucy A. Godley, Kim E. Nichols, et al.
Cancer Discovery (2024) Vol. 14, Iss. 3, pp. 396-405
Open Access | Times Cited: 5
Idiopathic aplastic anemia vs hypocellular myelodysplastic syndrome
Jibran Durrani, Jaroslaw P. Maciejewski
Hematology (2019) Vol. 2019, Iss. 1, pp. 97-104
Open Access | Times Cited: 37
Jibran Durrani, Jaroslaw P. Maciejewski
Hematology (2019) Vol. 2019, Iss. 1, pp. 97-104
Open Access | Times Cited: 37
Germline predisposition traits in allogeneic hematopoietic stem-cell transplantation for myelodysplastic syndromes: a survey-based study and position paper on behalf of the Chronic Malignancies Working Party of the EBMT
Carmelo Gurnari, Marie Robin, Lucy A. Godley, et al.
The Lancet Haematology (2023) Vol. 10, Iss. 12, pp. e994-e1005
Closed Access | Times Cited: 12
Carmelo Gurnari, Marie Robin, Lucy A. Godley, et al.
The Lancet Haematology (2023) Vol. 10, Iss. 12, pp. e994-e1005
Closed Access | Times Cited: 12
Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome
Hironori Arai, Hirotaka Matsui, SungGi Chi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 1, pp. 652-652
Open Access | Times Cited: 4
Hironori Arai, Hirotaka Matsui, SungGi Chi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 1, pp. 652-652
Open Access | Times Cited: 4
Germline predisposition to hematopoietic malignancies
Simone Feurstein, Michael W. Drazer, Lucy A. Godley
Human Molecular Genetics (2021) Vol. 30, Iss. R2, pp. R225-R235
Open Access | Times Cited: 25
Simone Feurstein, Michael W. Drazer, Lucy A. Godley
Human Molecular Genetics (2021) Vol. 30, Iss. R2, pp. R225-R235
Open Access | Times Cited: 25
Stopping Leukemia in Its Tracks: Should Preemptive Hematopoietic Stem-Cell Transplantation be Offered to Patients at Increased Genetic Risk for Acute Myeloid Leukemia?
Kayla V. Hamilton, Luke Maese, Jonathan M. Marron, et al.
Journal of Clinical Oncology (2019) Vol. 37, Iss. 24, pp. 2098-2104
Closed Access | Times Cited: 26
Kayla V. Hamilton, Luke Maese, Jonathan M. Marron, et al.
Journal of Clinical Oncology (2019) Vol. 37, Iss. 24, pp. 2098-2104
Closed Access | Times Cited: 26
Assessment of technical heterogeneity among diagnostic tests to detect germline risk variants for hematopoietic malignancies
Gregory W. Roloff, Lucy A. Godley, Michael W. Drazer
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 211-214
Open Access | Times Cited: 24
Gregory W. Roloff, Lucy A. Godley, Michael W. Drazer
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 211-214
Open Access | Times Cited: 24
Acute Myeloid Leukaemia
FRACP Barbara J. Bain MB BS, FRCP Mike Leach MB ChB
(2024), pp. 141-270
Closed Access | Times Cited: 3
FRACP Barbara J. Bain MB BS, FRCP Mike Leach MB ChB
(2024), pp. 141-270
Closed Access | Times Cited: 3
Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome
Jörg Cammenga
Experimental Hematology (2024) Vol. 134, pp. 104217-104217
Open Access | Times Cited: 3
Jörg Cammenga
Experimental Hematology (2024) Vol. 134, pp. 104217-104217
Open Access | Times Cited: 3
Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7
Masanori Yoshida, Kanako Tanase‐Nakao, Hirohito Shima, et al.
British Journal of Haematology (2020) Vol. 191, Iss. 5, pp. 835-843
Open Access | Times Cited: 23
Masanori Yoshida, Kanako Tanase‐Nakao, Hirohito Shima, et al.
British Journal of Haematology (2020) Vol. 191, Iss. 5, pp. 835-843
Open Access | Times Cited: 23
Mechanisms of somatic transformation in inherited bone marrow failure syndromes
Haruna B. Choijilsuren, Yeji Park, Moonjung Jung
Hematology (2021) Vol. 2021, Iss. 1, pp. 390-398
Open Access | Times Cited: 19
Haruna B. Choijilsuren, Yeji Park, Moonjung Jung
Hematology (2021) Vol. 2021, Iss. 1, pp. 390-398
Open Access | Times Cited: 19
The Genomics of Myelodysplastic Syndromes: Origins of Disease Evolution, Biological Pathways, and Prognostic Implications
Hassan Awada, Bicky Thapa, Valeria Visconte
Cells (2020) Vol. 9, Iss. 11, pp. 2512-2512
Open Access | Times Cited: 18
Hassan Awada, Bicky Thapa, Valeria Visconte
Cells (2020) Vol. 9, Iss. 11, pp. 2512-2512
Open Access | Times Cited: 18
Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromes
Joseph H. Oved, Daria V. Babushok, Michele P. Lambert, et al.
Blood Advances (2020) Vol. 4, Iss. 20, pp. 5232-5245
Open Access | Times Cited: 12
Joseph H. Oved, Daria V. Babushok, Michele P. Lambert, et al.
Blood Advances (2020) Vol. 4, Iss. 20, pp. 5232-5245
Open Access | Times Cited: 12
Sticky, Adaptable, and Many‐sided: SAM protein versatility in normal and pathological hematopoietic states
Suhita Ray, Kyle J. Hewitt
BioEssays (2023) Vol. 45, Iss. 8
Open Access | Times Cited: 4
Suhita Ray, Kyle J. Hewitt
BioEssays (2023) Vol. 45, Iss. 8
Open Access | Times Cited: 4
Needle in a haystack or elephant in the room? Identifying germline predisposition syndromes in the setting of a new myeloid malignancy diagnosis
Erica Reinig, Jeremy D. Rubinstein, Apoorva T. Patil, et al.
Leukemia (2023) Vol. 37, Iss. 8, pp. 1589-1599
Open Access | Times Cited: 4
Erica Reinig, Jeremy D. Rubinstein, Apoorva T. Patil, et al.
Leukemia (2023) Vol. 37, Iss. 8, pp. 1589-1599
Open Access | Times Cited: 4