Purvi M. Kakadia - Concepedia

Author

Purvi M. Kakadia

Also Known As

P M Kakadia, P. Kakadia, P. M. Kakadia, P.M. Kakadia, Purvi Kakadia, Purvi M Kakadia, Purvi M. Kakadia, Purvi M. Kakadia, Stephanie Schneider

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München University of Auckland Helmholtz Zentrum München Philipps University of Marburg University of Münster

About

Purvi M. Kakadia is an author at Ludwig-Maximilians-Universität München specializing in medicine, cell biology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	433
2	Cell Biology	5	5	353
3	Immunology	4	4	179
4	Health Sciences	3	3	151
5	Molecular Genetics	1	1	174

Purvi M. Kakadia

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta Lutz Garbes, Kyung‐Ho Kim, Angelika Rieß, The American Journal of Human Genetics Developmental BiologyCell DivisionBone Morphogenic ProteinGenetic DisorderGenetics	2015	174
GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia Philipp A. Greif, Annika Dufour, Nikola P. Konstandin, Blood	2012	147
Acute myeloid leukemia is propagated by a leukemic stem cell with lymphoid characteristics in a mouse model of CALM/AF10-positive leukemia Aniruddha J. Deshpande, Monica Cusan, Vijay P.S. Rawat, Cancer Cell Hematological MalignancyMedicineAcute Myeloid LeukemiaMixed-phenotype Acute LeukemiaImmunology	2006	125
Combined Molecular and Clinical Prognostic Index for Relapse and Survival in Cytogenetically Normal Acute Myeloid Leukemia Friederike Pastore, Annika Dufour, Tobias Benthaus, Journal of Clinical Oncology	2014	113
Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis Tobias Herold, Klaus H. Metzeler, Sebastian Vosberg, Blood	2014	104
RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes Philipp A. Greif, Nikola P. Konstandin, Klaus H. Metzeler, Haematologica	2012	98
Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML (NK-AML) Friederike Schneider, Eva Hoster, Stephanie Schneider, Annals of Hematology Age-dependent FrequenciesGenetic DisorderMedicineGeneticsNormal Karyotype Aml	2011	80
Rapid and sensitive screening for <i>CEBPA</i> mutations in acute myeloid leukaemia Tobias Benthaus, Friederike Schneider, Gudrun Mellert, British Journal of Haematology	2008	69
Global reduction of the epigenetic H3K79 methylation mark and increased chromosomal instability in CALM-AF10–positive leukemias Yi-Hui Lin, Purvi M. Kakadia, Ying Chen, Blood	2009	65
Evofosfamide for the treatment of human papillomavirus-negative head and neck squamous cell carcinoma Stephen M. F. Jamieson, Peter Tsai, Maria Kondratyev, JCI Insight	2018	58

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