Connection
Srinivas Ramachandran to Male
This is a "connection" page, showing publications Srinivas Ramachandran has written about Male.
|
|
| |
Connection Strength |
|
 |
|
 |
| |
0.022 |
|
|
|
-
Thakran S, Guin D, Singh P, Uppili B, Ramachandran S, Kushwaha SS, Kukreti R. Genome-Wide Association Study Reveals Genetic Architecture of Common Epilepsies. Clin Genet. 2025 07; 108(1):22-32.
Score: 0.008
-
Valdes P, Caldwell AB, Liu Q, Fitzgerald MQ, Ramachandran S, Karch CM, Galasko DR, Yuan SH, Wagner SL, Subramaniam S. Integrative multiomics reveals common endotypes across PSEN1, PSEN2, and APP mutations in familial Alzheimer's disease. Alzheimers Res Ther. 2025 01 04; 17(1):5.
Score: 0.008
-
Vats A, Gourie-Devi M, Verma M, Ramachandran S, Taneja B, Kukreti R, Taneja V. Identification of L84F mutation with a novel nucleotide change c.255G?>?T in the superoxide dismutase gene in a North Indian family with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener. 2016; 17(3-4):253-9.
Score: 0.004
-
Sharma A, Sharma VK, Horn-Saban S, Lancet D, Ramachandran S, Brahmachari SK. Assessing natural variations in gene expression in humans by comparing with monozygotic twins using microarrays. Physiol Genomics. 2005 Mar 21; 21(1):117-23.
Score: 0.002
|
Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
|