Luba Kalaydjieva

Mosaicism for a missense SCN1A mutation and borderline Dravet syndrome in a Roma/Gypsy family

Josemir W. Sander, Laura Florez, Ingrid E. Scheffer, 2010 .

Impact of the Reelin signaling cascade (Ligands–Receptors–Adaptor Complex) on cognition in schizophrenia

Steven Wiltshire, Leon Flicker, Luba Kalaydjieva, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

RefGenes: identification of reliable and condition specific reference genes for RT-qPCR data normalization

Tomas Hruz, Wilhelm Gruissem, Philip Zimmermann, 2011, BMC Genomics.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.

Luba Kalaydjieva, Assen Jablensky, Patricia T Michie, 2005, American journal of human genetics.

The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time.

Giovanni Destro-Bisol, David Gresham, Marcus W Feldman, 2004, American journal of human genetics.

Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease

Hanns Lochmüller, Thomas Voit, P K Thomas, 2003, Human mutation.