viswateja nelakuditi
viswateja nelakuditi
Bioinformatician
Email verificata su bsd.uchicago.edu
Titolo
Citata da
Citata da
Anno
Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach
G Alkorta-Aranburu, D Carmody, YW Cheng, V Nelakuditi, L Ma, ...
Molecular genetics and metabolism 113 (4), 315-320, 2014
802014
Expanding the boundaries of RNA sequencing as a diagnostic tool for rare mendelian disease
HD Gonorazky, S Naumenko, AK Ramani, V Nelakuditi, P Mashouri, ...
The American Journal of Human Genetics 104 (3), 466-483, 2019
692019
A computational genomics pipeline for prokaryotic sequencing projects
AO Kislyuk, LS Katz, S Agrawal, MS Hagen, AB Conley, P Jayaraman, ...
Bioinformatics 26 (15), 1819-1826, 2010
672010
Frequency of germline mutations in cancer susceptibility genes in malignant mesothelioma
V Panou, M Gadiraju, A Wolin, CM Weipert, E Skarda, AN Husain, ...
Journal of Clinical Oncology 36 (28), 2863, 2018
612018
Supercomputing for the parallelization of whole genome analysis
MJ Puckelwartz, LL Pesce, V Nelakuditi, L Dellefave-Castillo, JR Golbus, ...
Bioinformatics 30 (11), 1508-1513, 2014
602014
Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy
JR Golbus, MJ Puckelwartz, L Dellefave-Castillo, JP Fahrenbach, ...
Circulation: Cardiovascular Genetics 7 (6), 751-759, 2014
472014
Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes
L Guidugli, AK Johnson, G Alkorta-Aranburu, V Nelakuditi, K Arndt, ...
Leukemia 31 (5), 1226-1229, 2017
272017
Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes
M Sun, AK Johnson, V Nelakuditi, L Guidugli, D Fischer, K Arndt, L Ma, ...
Genetics in Medicine 21 (1), 195-206, 2019
232019
Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals
KL Yap, AEK Johnson, D Fischer, P Kandikatla, J Deml, V Nelakuditi, ...
Genetics in Medicine 21 (1), 233-242, 2019
192019
Characterization of patients referred for non‐specific intellectual disability testing: the importance of autosomal genes for diagnosis
CA Tan, S Topper, D Del Gaudio, V Nelakuditi, O Shchelochkov, ...
Clinical genetics 89 (4), 478-483, 2016
142016
Neisseria Base: a comparative genomics database for Neisseria meningitidis
LS Katz, JC Humphrey, AB Conley, V Nelakuditi, AO Kislyuk, S Agrawal, ...
Database 2011, 2011
112011
Correction:“Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals”
KL Yap, AEK Johnson, D Fischer, P Kandikatla, J Deml, V Nelakuditi, ...
Genetics in Medicine 21 (1), 262-265, 2019
22019
Identification of genetic hereditary predisposition to hematologic malignancies by clinical next-generation sequencing
AE Knight Johnson, L Guidugli, K Arndt, G Alkorta-Aranburu, V Nelakuditi, ...
Blood, The Journal of the American Society of Hematology 126 (23), 3854-3854, 2015
22015
OCHROdb: a comprehensive, quality checked database of open chromatin regions from sequencing data
P Shooshtari, S Feng, V Nelakuditi, J Foong, M Brudno, C Cotsapas
bioRxiv, 484840, 2018
12018
A computational genomics pipeline for microbial sequencing projects
AO Kislyuk, LS Katz, S Agrawal, MS Hagen, AB Conley, P Jayaraman, ...
12005
FORCAST: a fully integrated and open source pipeline to design Cas-mediated mutagenesis experiments
H Elrick, V Nelakuditi, G Clark, M Brudno, AK Ramani, LMJ Nutter
bioRxiv, 2020
2020
Pouria Mashouri, 2 Peiqui Wang, 2 Dennis Kao, 2 Krish Ohri, 3 Senthuri Viththiyapaskaran, 3 Mark A. Tarnopolsky, 4 Katherine D. Mathews, 5 Steven A. Moore, 6 Andres N. Osorio …
HD Gonorazky, S Naumenko, AK Ramani, V Nelakuditi
The American Journal of Human Genetics 104, 466-483, 2019
2019
DDX41is the Most Common Gene Predisposed to Hereditary Myeloid Malignancies.:[3]
M Leung, A Johnson, K Arndt, V Nelakuditi, D del Gaudio, S Das, Z Li
Annals of Clinical & Laboratory Science 48 (3), 2018
2018
Improved Diagnosis for Familial Myelodysplastic Syndromes and Acute Leukemia Using Next-generation Sequencing and Splicing Analysis
L Guidugli, AK Johnson, G Alkorta-Aranburu, V Nelakuditi, K Arndt, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 17 (6), 772-772, 2015
2015
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–19