Gabriela M. Baerlocher

Author

Also Known As

A Gratwohl, Baerlocher, Gabriela M., Dominik Heim, G BAERLOCHER, G Baerlocher, G M Baerlocher, G Schlimok, G. Baerlocher, G. M. Baerlocher, G.M. Baerlocher

208

Publications

9.3K

Citations

H-Index

Concepts

All Affiliations

University Hospital of Bern University of Bern University of British Columbia BC Cancer Agency Heidelberg University

About

Gabriela M. Baerlocher is an author at University Hospital of Bern specializing in medicine, cell biology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	29	2.4K
2	Health Sciences	10	11	609
3	Engineering	2	2	172
4	Biology	2	2	838
5	Natural Sciences	1	1	401

Gabriela M. Baerlocher

Publications

8.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in <i>TERT,</i> the Gene for Telomerase Reverse Transcriptase, in Aplastic Anemia Hiroki Yamaguchi, Rodrigo T. Calado, Hinh Ly, New England Journal of Medicine	2005	711
Extension of Cell Life-Span and Telomere Length in Animals Cloned from Senescent Somatic Cells Robert Lanza, José B. Cibelli, Catherine Blackwell, Science	2000	467
Flow cytometry and FISH to measure the average length of telomeres (flow FISH) Gabriela M. Baerlocher, Irma Vulto, Gary de Jong, Nature Protocols BiologyFlow CytometryAverage LengthBiostatisticsCytometry	2006	437
Interactions between Siglec-7/9 receptors and ligands influence NK cell–dependent tumor immunosurveillance Camilla Jandus, Kayluz Frias Boligan, Obinna Chijioke, Journal of Clinical Investigation	2014	424
Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML) Benjamin Hanfstein, Marc Müller, Rüdiger Hehlmann, Leukemia Hematological MalignancyChronic Myeloid LeukemiaHealth SciencesMedicineHematology	2012	416
TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita Sharon A. Savage, Neelam Giri, Gabriela M. Baerlocher, The American Journal of Human Genetics BiologyIs MutatedNatural SciencesGeneticsDyskeratosis Congenita	2008	401
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita Blanche P. Alter, Gabriela M. Baerlocher, Sharon A. Savage, Blood	2007	346
Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome Hiroki Yamaguchi, Gabriela M. Baerlocher, Peter M. Lansdorp, Blood	2003	303
Deep Molecular Response Is Reached by the Majority of Patients Treated With Imatinib, Predicts Survival, and Is Achieved More Quickly by Optimized High-Dose Imatinib: Results From the Randomized CML-Study IV Rüdiger Hehlmann, Martin C. Müller, Michael Lauseker, Journal of Clinical Oncology	2013	296
Impact of additional cytogenetic aberrations at diagnosis on prognosis of CML: long-term observation of 1151 patients from the randomized CML Study IV Alice Fabarius, Armin Leitner, Andreas Hochhaus, Blood	2011	286

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