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Anushree Bharadwaj
51
results:
Search for persons
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Online (51)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (29)
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1
The Wnt-pathway corepressor TLE3 interacts with the histone..:
Kalita, Bhargab
;
Sahu, Subhashni
;
Bharadwaj, Anushree
...
Oncogene. 43 (2024) 7 - p. 524-538 , 2024
Link:
https://doi.org/10.1038/..
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2
Musculoskeletal defects associated with myosin heavy chain‐..:
Bharadwaj, Anushree
;
Sharma, Jaydeep
;
Singh, Jagriti
...
EMBO Molecular Medicine. 15 (2023) 9 - p. , 2023
Link:
https://doi.org/10.15252..
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3
Ribosome‐associated quality control mediates degradation of..:
Pradhan, Ashis Kumar
;
Kandasamy, Ganapathi
;
Chatterjee, Upasana
...
FEBS Letters. 595 (2021) 15 - p. 2015-2033 , 2021
Link:
https://doi.org/10.1002/..
?
4
Musculoskeletal defects associated with myosin heavy chain‐..:
Anushree Bharadwaj
;
Jaydeep Sharma
;
Jagriti Singh
...
https://doi.org/10.15252/emmm.202217187. , 2023
Link:
https://doi.org/10.15252..
?
5
Musculoskeletal defects associated with myosin heavy chain‐..:
Bharadwaj, Anushree
;
Sharma, Jaydeep
;
Singh, Jagriti
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493586/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
6
Myosin heavy chain-embryonic regulates skeletal muscle diff..:
Agarwal, Megha
;
Sharma, Akashi
;
Kumar, Pankaj
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157585/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
7
Heterogeneous genetic patterns in bilateral perisylvian pol..:
Järvelä, Irma
;
Paetau, Ritva
;
Rajendran, Yasmin
...
Brain Communications. 6 (2024) 3 - p. , 2024
Link:
https://doi.org/10.1093/..
?
8
A Novel Variant in VPS13B Underlying Cohen Syndrome:
Hussain, Abrar
;
Acharya, Anushree
;
Bharadwaj, Thashi
...
BioMed Research International. 2023 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1155/..
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9
Variants in EFCAB7 underlie nonsyndromic postaxial polydact..:
Bilal, Muhammad
;
Khan, Hammal
;
Khan, Muhammad Javed
...
European Journal of Human Genetics. 31 (2023) 11 - p. 1270-1274 , 2023
Link:
https://doi.org/10.1038/..
?
10
Nonsense variant in a consanguineous family expands the phe..:
Liaqat, Khurram
;
Bharadwaj, Thashi
;
Shah, Khadim
...
Clinical Genetics. 104 (2023) 4 - p. 499-501 , 2023
Link:
https://doi.org/10.1111/..
?
11
A novel variant in CYFIP2 in a girl with severe disabilitie..:
Salokivi, Tommi
;
Parkkola, Riitta
;
Rajendran, Yasmin
...
American Journal of Medical Genetics Part A. 194 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1002/..
?
12
Phenotype Expansion for Atypical Gaucher Disease Due to Hom..:
Liaqat, Khurram
;
Hussain, Shabir
;
Acharya, Anushree
...
Genes. 13 (2022) 4 - p. 662 , 2022
Link:
https://doi.org/10.3390/..
?
13
A novel autosomal dominant GREB1L variant associated with n..:
Adadey, Samuel Mawuli
;
Aboagye, Elvis Twumasi
;
Esoh, Kevin
...
BMC Medical Genomics. 15 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
14
Exome sequencing of families from Ghana reveals known and c..:
Wonkam, Ambroise
;
Adadey, Samuel Mawuli
;
Schrauwen, Isabelle
...
Communications Biology. 5 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
15
SCN1A Variants as the Underlying Cause of Genetic Epilepsy ..:
Cornejo-Sanchez, Diana M.
;
Acharya, Anushree
;
Bharadwaj, Thashi
...
Genes. 13 (2022) 5 - p. 754 , 2022
Link:
https://doi.org/10.3390/..
1-15