Harendra Guturu - Concepedia

Author

Harendra Guturu

Also Known As

Analysis Team Lead, Asher Haug Baltzell, Asher K Haug Baltzell, Asher K. Haug Baltzell, Chris C. A. Spencer, Crawford, Gregory E., Guturu, Harendra, H Guturu, H. Guturu, Harendra Guturu

Publications

4.4K

Citations

H-Index

Concepts

All Affiliations

Stanford University Geisinger Medical Center Stanford Medicine Cardiff University University of Pennsylvania

About

Harendra Guturu is an author at Stanford University specializing in medicine, genetics, and biostatistics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1.5K
2	Natural Sciences	4	4	169
3	Public Health	3	3	982
4	Biology	2	2	111
5	Social Sciences	1	1	38

Harendra Guturu

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, Nature Genetics High SensitivityUncertain SignificanceMedicineGenetic EpidemiologyPathology	2016	902
Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers Aaron M. Wenger, Harendra Guturu, Jonathan A. Bernstein, Genetics in Medicine InfertilityDiagnosisGynecologyBiostatisticsMenopause	2016	316
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease Julie Horowitz, Jack A. Kosmicki, Amy Damask, Nature Genetics	2022	174
Microbiota modulate transcription in the intestinal epithelium without remodeling the accessible chromatin landscape J. Gray Camp, Christopher L. Frank, Colin R. Lickwar, Genome Research	2014	166
BioText Search Engine: beyond abstract search Marti A. Hearst, Anna Divoli, Harendra Guturu, Bioinformatics	2007	156
Clustering of 770,000 genomes reveals post-colonial population structure of North America Eunjung Han, Peter Carbonetto, Ross E. Curtis, Nature Communications	2017	119
AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature Johannes Birgmeier, Maximilian Haeussler, Cole A. Deisseroth, Science Translational Medicine	2020	117
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly Diana Alcantara, Andrew E. Timms, Karen W. Gripp, Brain	2017	110
Computational methods to detect conserved non-genic elements in phylogenetically isolated genomes: application to zebrafish Michael Hiller, Saatvik Agarwal, James H. Notwell, Nucleic Acids Research Comparative GenomicsGeneticsGenomicsPhylogenetic AnalysisPhylogenetics	2013	91
Phrank measures phenotype sets similarity to greatly improve Mendelian diagnostic disease prioritization Karthik A. Jagadeesh, Johannes Birgmeier, Harendra Guturu, Genetics in Medicine Mendelian DisorderVariant InterpretationMedicineGeneticsGenetic Epidemiology	2018	57

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