E. Michael Gertz - Concepedia

Author

E. Michael Gertz

Also Known As

E Gertz, E M Gertz, E Michael Gertz, E. M. Gertz, E. Michael Gertz, E. Michael Gertz, Edward Gertz, Edward Michael Gertz, Emilie Gertz, Gertz, E. Michael

152

Publications

7.2K

Citations

H-Index

Concepts

All Affiliations

National Institutes of Health National Center for Biotechnology Information National Cancer Institute Center for Cancer Research University Medical Center Freiburg

About

E. Michael Gertz is an author at National Institutes of Health specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	1.1K
2	Natural Sciences	5	5	791
3	Engineering	4	4	351
4	Public Health	2	2	74
5	Health Sciences	1	1	27

E. Michael Gertz

Publications

Citations

H-Index

Page 1

	Year	Citations
Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor Erik‐Oliver Glocker, Daniel Kotlarz, Kaan Boztuǧ, New England Journal of Medicine	2009	1.4K
Composition-based statistics and translated nucleotide searches: Improving the TBLASTN module of BLAST E. Michael Gertz, Yi‐Kuo Yu, Richa Agarwala, BMC Biology	2006	594
A Fast and Symmetric DUST Implementation to Mask Low-Complexity DNA Sequences Aleksandr Morgulis, E. Michael Gertz, Alejandro A. Schäffer, Journal of Computational Biology GeneticsDna AnalysisMolecular BiologyGenomicsSequence Design	2006	529
Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity Gabriela López‐Herrera, Giacomo Tampella, Qiang Pan‐Hammarström, The American Journal of Human Genetics	2012	513
WindowMasker: window-based masker for sequenced genomes Aleksandr Morgulis, E. Michael Gertz, Alejandro A. Schäffer, Bioinformatics	2005	353
The phenotype of human STK4 deficiency Hengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, Blood	2012	321
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome Cristina Woellner, E. Michael Gertz, Alejandro A. Schäffer, Journal of Allergy and Clinical Immunology Mendelian DisorderGenetic DisorderPathologyMolecular DiagnosticsDiagnostic Guidelines	2010	313
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, Blood	2008	274
Object-oriented software for quadratic programming E. Michael Gertz, Stephen J. Wright ACM Transactions on Mathematical Software Mathematical ProgrammingOoqp DistributionEngineeringObject-oriented ModelingSoftware Engineering	2003	253
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome Daniel Kotlarz, Natalia Ziętara, Gülbû Uzel, The Journal of Experimental Medicine	2013	214

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