Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Hahn, Christopher N
3121  Ergebnisse:
Personensuche X
?
1

IDH-mutant myeloid neoplasms are associated with seronegati..:

Hong, Lih En ; Wechalekar, Mihir D. ; Kutyna, Monika...
Blood.  143 (2024)  18 - p. 1873-1877 , 2024
Link: https://doi.org/10.1182/..
 
?
2

The 10th Barossa meeting: Cell Signalling to Cancer Medicin:

Kan, Winnie L. ; McClure, Barbara J. ; Hahn, Christopher N..
Cell Death & Disease.  15 (2024)  3 - p. , 2024
Link: https://doi.org/10.1038/..
 
?
3

Allogeneic hematopoietic stem cell transplant outcomes in a..:

Saygin, Caner ; Roloff, Gregory ; Hahn, Christopher N....
Blood Advances.  7 (2023)  4 - p. 549-554 , 2023
Link: https://doi.org/10.1182/..
 
?
4

Novel modes of MPL activation in triple-negative myeloproli..:

Samaraweera, Saumya E. ; Geukens, Tatjana ; Casolari, Debora A....
Pathology.  55 (2023)  1 - p. 77-85 , 2023
Link: https://doi.org/10.1016/..
 
?
5

Transcription factor genetics and biology in predisposition..:

Zerella, Jiarna R. ; Homan, Claire C. ; Arts, Peer...
Frontiers in Oncology.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
?
6

TP53 mutation variant allele frequency of ≥10% is associate..:

Shah, Mithun Vinod ; Tran, Elizabeth Ngoc Hoa ; Shah, Syed...
Blood Cancer Journal.  13 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
?
7

Clonal hematopoiesis in patients with ANKRD26 or ETV6 germl..:

Drazer, Michael W. ; Homan, Claire C. ; Yu, Kai...
Blood Advances.  6 (2022)  15 - p. 4357-4359 , 2022
Link: https://doi.org/10.1182/..
 
?
8

Role of Germline Predisposition to Therapy-Related Myeloid ..:

Baranwal, Anmol ; Hahn, Christopher N. ; Shah, Mithun Vinod.
Current Hematologic Malignancy Reports.  17 (2022)  6 - p. 254-265 , 2022
Link: https://doi.org/10.1007/..
 
?
9

A practical guide to interpreting germline variants that dr..:

Feurstein, Simone ; Hahn, Christopher N. ; Mehta, Nikita.
Genetics in Medicine.  24 (2022)  4 - p. 931-954 , 2022
Link: https://doi.org/10.1016/..
 
?
10

Cover, Volume 42, Issue 11:

Homan, Claire C. ; Venugopal, Parvathy ; Arts, Peer...
Human Mutation.  42 (2021)  11 - p. , 2021
Link: https://doi.org/10.1002/..
 
?
11

Targeted gene panels identify a high frequency of pathogeni..:

Singhal, Deepak ; Hahn, Christopher N. ; Feurstein, Simone...
Leukemia.  35 (2021)  11 - p. 3245-3256 , 2021
Link: https://doi.org/10.1038/..
 
?
12

GATA2 deficiency syndrome: A decade of discovery:

Homan, Claire C. ; Venugopal, Parvathy ; Arts, Peer...
Human Mutation.  42 (2021)  11 - p. 1399-1421 , 2021
Link: https://doi.org/10.1002/..
 
?
13

A synonymousGATA2variant underlying familial myeloid malign..:

Fox, Lucy C. ; Tan, Michelle ; Brown, Anna L....
British Journal of Haematology.  190 (2020)  5 - p. , 2020
Link: https://doi.org/10.1111/..
 
?
14

Two monogenic disorders masquerading as one: severe congeni..:

Venugopal, Parvathy ; Gagliardi, Lucia ; Forsyth, Cecily...
BMC Medical Genetics.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
?
15

RUNX1-mutated families show phenotype heterogeneity and a s..:

Scott, Hamish S. ; Hahn, Christopher N. ; Poplawski, Nicola K....
Blood Advances.  4 (2020)  6 - p. 1131-1144 , 2020
Link: https://doi.org/10.1182/..
 
1-15