Luba Kalaydjieva - Concepedia

Author

Luba Kalaydjieva

Harry Perkins Institute of Medical Research

Also Known As

Ames, David, Clement C. Zai, Conrad Iyegbe, David Kavanagh, Erik Söderman, Juha Karjalainen, Kalaydjieva L, Kalaydjieva, L, Kalaydjieva, Luba, L Kalaydjieva

193

Publications

13.6K

Citations

H-Index

158

Concepts

All Affiliations

Harry Perkins Institute of Medical Research The University of Western Australia Medical University of Sofia Edith Cowan University University College London

About

Luba Kalaydjieva is an author at Harry Perkins Institute of Medical Research specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	65	8.1K
2	Engineering	3	3	1.5K
3	Health Sciences	2	2	37
4	Language Studies	2	2	91
5	Education	1	1	206

Luba Kalaydjieva

109

Publications

12.3K

Citations

H-Index

Page 1

	Year	Citations
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores Bjarni J. Vilhjálmsson, Jian Yang, Hilary K. Finucane, The American Journal of Human Genetics Linkage DisequilibriumEngineeringPolygenic RiskRisk ManagementPolygenic Risk Scores	2015	1.5K
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Nature Genetics PsychiatryGeneticsPsychiatric GeneticsGenetic EpidemiologyCopy Number Variants	2016	1.1K
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, Cell PsychiatryPsychotic DisorderGeneticsSchizophreniaSocial Sciences	2018	797
A Genomic Screen of Autism: Evidence for a Multilocus Etiology Neil Risch, Donna Spiker, Linda Lotspeich, The American Journal of Human Genetics Neurodevelopmental DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	1999	687
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases Alexander Gusev, Sang Lee, Gosia Trynka, The American Journal of Human Genetics Genome-wide Association StudyAllelic VariantPhenotypic VariationGenotype-phenotype AssociationMedicine	2014	639
Y-Chromosomal Diversity in Europe Is Clinal and Influenced Primarily by Geography, Rather than by Language Zoë H. Rosser, Tatiana Zerjal, Matthew E. Hurles, The American Journal of Human Genetics Europe Is ClinalHuman VariationCytogeneticsNatural SciencesGenetics	2000	617
The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time Lev A. Zhivotovsky, Peter A. Underhill, Cengiz Cinnioğlu, The American Journal of Human Genetics Linkage DisequilibriumMolecular EcologyEffective Mutation RateMedicineGenetics	2004	397
The origin of the major cystic fibrosis mutation (ΔF508) in European populations Núria Morral, Jaume Bertranpetit, Xavier Estivill, Nature Genetics FibrosisMendelian DisorderGenetic DisorderGeneticsPathogenesis	1994	343
Null Mutations in LTBP2 Cause Primary Congenital Glaucoma Manir Ali, Martin McKibbin, Adam Booth, The American Journal of Human Genetics Mendelian DisorderOphthalmologyNull MutationsGenetic DisorderGenetics	2009	322
RefGenes: identification of reliable and condition specific reference genes for RT-qPCR data normalization Tomáš Hrúz, Markus Wyss, Mylène Docquier, BMC Genomics	2011	294

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