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Ramprasad, Vedam L
90
results:
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Online (90)
Mediatypes
Articles (Online) (42)
OpenAccess-fulltext (48)
Sorted by: Relevance
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1
Comprehensive germline profiling of patients with breast ca..:
Pramanik, Raja
;
Chitikela, Sindhura
;
Deo, SVS
...
ecancermedicalscience. 18 (2024) - p. , 2024
Link:
https://doi.org/10.3332/..
?
2
Comprehensive laboratory diagnosis of Fanconi anaemia: comp..:
Joshi, Gaurav
;
Arthur, Nancy Beryl Janet
;
Geetha, Thenral S
...
Journal of Medical Genetics. 60 (2023) 8 - p. 801-809 , 2023
Link:
https://doi.org/10.1136/..
?
3
Identification of a shared, common haplotype segregating wi..:
Sanga, Shamita
;
Chakraborty, Sudipta
;
Bardhan, Mainak
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
4
Molecular epidemiology of SARS-CoV-2 in healthcare workers ..:
Bhattacharya, Sanjay
;
Chatterji, Soumyadip
;
Chandy, Mammen
...
Indian Journal of Medical Microbiology. 41 (2023) - p. 104-110 , 2023
Link:
https://doi.org/10.1016/..
?
5
Genome‐Wide Polygenic Score Predicts Large Number of High R..:
Kukkle, Prashanth Lingappa
;
Geetha, Thenral S.
;
Chaudhary, Ruchi
...
Advanced Biology. 6 (2022) 11 - p. , 2022
Link:
https://doi.org/10.1002/..
?
6
Genotype–phenotype correlation and natural history study of..:
Nashi, Saraswati
;
Polavarapu, Kiran
;
Bardhan, Mainak
...
neurogenetics. 24 (2022) 1 - p. 43-53 , 2022
Link:
https://doi.org/10.1007/..
?
7
Clinical, genetic profile and disease progression of sarcog..:
Bardhan, Mainak
;
Anjanappa, Ram Murthy
;
Polavarapu, Kiran
...
neurogenetics. 23 (2022) 3 - p. 187-202 , 2022
Link:
https://doi.org/10.1007/..
?
8
Oculogyric Crisis Phenotype of Levodopa‐Induced Ocular Dysk..:
Olszewska, Diana A.
;
Shetty, Rajesh
;
Geetha, Thenral S.
...
Movement Disorders Clinical Practice. 9 (2022) 3 - p. 390-393 , 2022
Link:
https://doi.org/10.1002/..
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9
Growth and neurodevelopmental disorder with arthrogryposis,..:
Bijarnia-Mahay, Sunita
;
Somashekar, Puneeth H.
;
Kaur, Parneet
...
Journal of Human Genetics. 67 (2021) 3 - p. 133-136 , 2021
Link:
https://doi.org/10.1038/..
?
10
Clinical Study of 668 Indian Subjects with Juvenile, Young,..:
Kukkle, Prashanth L.
;
Goyal, Vinay
;
Geetha, Thenral S.
...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49 (2021) 1 - p. 93-101 , 2021
Link:
https://doi.org/10.1017/..
?
11
Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Muta..:
Polavarapu, Kiran
;
Bardhan, Mainak
;
Anjanappa, Ram Murthy
...
Journal of Clinical Neurology. 17 (2021) 3 - p. 409 , 2021
Link:
https://doi.org/10.3988/..
?
12
Matrilineal analysis of mutations in the DMD gene in a mult..:
Shastry, Arun
;
Aravind, Sankaramoorthy
;
Sunil, Meeta
...
Molecular Genetics & Genomic Medicine. 9 (2021) 5 - p. , 2021
Link:
https://doi.org/10.1002/..
?
13
Retinoblastoma genetics screening and clinical management:
Gupta, Himika
;
Malaichamy, Sivasankar
;
Mallipatna, Ashwin
...
BMC Medical Genomics. 14 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
14
A Case of Autosomal Dominant Ataxia with Vocal Cord Palsy A..:
Kukkle, Prashanth L.
;
Geetha, Thenral S.
;
Mahadevan, Anita
.
Movement Disorders Clinical Practice. 7 (2020) 6 - p. 688-692 , 2020
Link:
https://doi.org/10.1002/..
?
15
Factor XIII Deficiency with a Novel Nonsense Mutation:
Khandelwal, Vipin
;
Sharma, Sanjeev Kumar
;
Doval, Divya
...
Indian Journal of Hematology and Blood Transfusion. 36 (2020) 3 - p. 588-589 , 2020
Link:
https://doi.org/10.1007/..
1-15