Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains
Blakey, R., Ranlund, S., Zartaloudi, E., Cahn, W., Calafato, S., Colizzi, M., Crespo-Facorro, B., Daniel, C., Díez-Revuelta, Á., Di Forti, M., Iyegbe, C., Jablensky, A., Jones, R., Hall, M.-H., Kahn, R., Kalaydjieva, L., Kravariti, E., Lin, K., McDonald, C., McIntosh, A. M., Picchioni, M., Powell, J., Presman, A., Rujescu, D., Schulze, K., Shaikh, M., Thygesen, J. H., Toulopoulou, T., Van Haren, N., Van Os, J., Walshe, M., Murray, R. M., Bramon, E.
Published in Psychological medicine (01.06.2018)
Published in Psychological medicine (01.06.2018)
Get full text
Journal Article
Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia
Jablensky, A., Morar, B., Wiltshire, S., Carter, K., Dragovic, M., Badcock, J. C., Chandler, D., Peters, K., Kalaydjieva, L.
Published in Genes, brain and behavior (01.06.2011)
Published in Genes, brain and behavior (01.06.2011)
Get full text
Journal Article
A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes
Gooding, R, Colomer, J, King, R, Angelicheva, D, Marns, L, Parman, Y, Chandler, D, Bertranpetit, J, Kalaydjieva, L
Published in Journal of medical genetics (01.12.2005)
Published in Journal of medical genetics (01.12.2005)
Get full text
Journal Article
Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia
Jablensky, A, Angelicheva, D, Donohoe, G J, Cruickshank, M, Azmanov, D N, Morris, D W, McRae, A, Weickert, C S, Carter, K W, Chandler, D, Alexandrov, B, Usheva, A, Morar, B, Verbrugghe, P L, Filipovska, A, Rackham, O, Bishop, A R, Rasmussen, K Ø, Dragovic, M, Cooper, M, Phillips, M, Badcock, J, Bramon-Bosch, E, Almeida, O P, Flicker, L, Gill, M, Corvin, A, MacGregor, S, Kalaydjieva, L
Published in Molecular psychiatry (01.12.2012)
Published in Molecular psychiatry (01.12.2012)
Get full text
Journal Article
The Gitelman syndrome mutation, IVS9+1G>T, is common across Europe
Bouwer, S.T., Coto, E., Santos, F., Angelicheva, D., Chandler, D., Kalaydjieva, L.
Published in Kidney international (01.10.2007)
Published in Kidney international (01.10.2007)
Get full text
Journal Article
Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies
Sivadorai, P, Cherninkova, S, Bouwer, S, Kamenarova, K, Angelicheva, D, Seeman, P, Hollingsworth, K, Mihaylova, V, Oscar, A, Dimitrova, G, Kaneva, R, Tournev, I, Kalaydjieva, L
Published in Clinical genetics (01.07.2008)
Published in Clinical genetics (01.07.2008)
Get full text
Journal Article
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks
CALAFELL, F., UNDERHILL, P., TOLUN, A., ANGELICHEVA, D., KALAYDJIEVA, L.
Published in Annals of human genetics (01.01.1996)
Published in Annals of human genetics (01.01.1996)
Get full text
Journal Article
Vlax Roma history: what do coalescent-based methods tell us?
CHAIX, R, AUSTERLITZ, F, MORAR, B, KALAYDJIEVA, L, HEYER, E
Published in European journal of human genetics : EJHG (01.04.2004)
Published in European journal of human genetics : EJHG (01.04.2004)
Get full text
Journal Article
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24
Hristova, Anna, Thomas, P.K, Savov, Alexey, Nikolova, Amelia, Angelicheva, Dora, Moskov, Momchil, King, Rosalind H. H, Middleton, Lefkos, Calafell, Francesc, Bittles, Alan H, Ishpekova, Boryana, Shmarov, Alexander, Petkova, Iva, Honeyman, K, Georgieva, Veneta, Chandler, David, Kalaydjieva, Luba, Hallmayer, Joachim, Turnev, Ivailo, Stancheva, Stella, Petrova, Julia
Published in Nature genetics (01.10.1996)
Published in Nature genetics (01.10.1996)
Get full text
Journal Article
The origin of the major cystic fibrosis mutation (ΔF508) in European populations
Russo, M.P, Restagno, G, Nemeti, M, Ferec, C, Varon-Mateeva, R, Angelicheva, D, Dancheva, R, Romeo, G, Garnerone, S, Schwarz, M, Morral, N, Schwartz, M, Nunes, V, Reis, A, Kalaydjieva, L, Dallapiccola, B, Ferrari, M, Kadasi, L, Novelli, G, Macek, M, de Arce, M, Giménez, J, Desgeorges, M, Estivill, X, Kere, J, Claustres, M, Casals, T, Dahl, N, Anvret, M, Magnani, C, Bertranpetit, J
Published in Nature genetics (01.06.1994)
Published in Nature genetics (01.06.1994)
Get full text
Journal Article
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes
Merlini, L, Gooding, R, Lochmüller, H, Müller-Felber, W, Walter, M C, Angelicheva, D, Talim, B, Hallmayer, J, Kalaydjieva, L
Published in Neurology (22.01.2002)
Published in Neurology (22.01.2002)
Get more information
Journal Article
Origins and Divergence of the Roma (Gypsies)
Gresham, David, Morar, Bharti, Underhill, Peter A., Passarino, Giuseppe, Lin, Alice A., Wise, Cheryl, Angelicheva, Dora, Calafell, Francesc, Oefner, Peter J., Shen, Peidong, Tournev, Ivailo, de Pablo, Rosario, Kuĉinskas, Vaidutis, Perez-Lezaun, Anna, Marushiakova, Elena, Popov, Vesselin, Kalaydjieva, Luba
Published in American journal of human genetics (01.12.2001)
Published in American journal of human genetics (01.12.2001)
Get full text
Journal Article
Severe neuropsychiatric symptoms in two siblings with intermediate type of Niemann-Pick disease
Mihaylova, V., Hantke, J., Cherninkova, S., Krastev, S., Radionova, M., Raicheva, M., Sinigerska, I., Jelev, H., Jablensky, A., Kalaydjieva, L., Tournev, I.
Published in Journal of neurology (01.09.2008)
Published in Journal of neurology (01.09.2008)
Get full text
Journal Article
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation
Merlini, L, Kaplan, J C, Navarro, C, Barois, A, Bonneau, D, Brasa, J, Echenne, B, Gallano, P, Jarre, L, Jeanpierre, M, Kalaydjieva, L, Leturcq, F, Levi-Gomes, A, Toutain, A, Tournev, I, Urtizberea, A, Vallat, J M, Voit, T, Warter, J M
Published in Neurology (14.03.2000)
Published in Neurology (14.03.2000)
Get more information
Journal Article
NMP08 Asymptomatic Charcot Marie Tooth
Rasic, V. Milic, Todorovic, S, Nelis, E, Keckarevic, M, Kalaydjieva, L, Brankovic, V
Published in European journal of paediatric neurology (2007)
Published in European journal of paediatric neurology (2007)
Get full text
Journal Article
Double mutant alleles: are they rare?
Savov, A, Angelicheva, D, Balassopoulou, A, Jordanova, A, Noussia-Arvanitakis, S, Kalaydjieva, L
Published in Human molecular genetics (01.07.1995)
Published in Human molecular genetics (01.07.1995)
Get more information
Journal Article
Genetic heterogeneity of polycystic kidney disease in Bulgaria
Bogdanova, N, Dworniczak, B, Dragova, D, Todorov, V, Dimitrakov, D, Kalinov, K, Hallmayer, J, Horst, J, Kalaydjieva, L
Published in Human genetics (01.06.1995)
Published in Human genetics (01.06.1995)
Get more information
Journal Article
Hereditary Motor and Sensory Neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies
Colomer, J, Iturriaga, C, Kalaydjieva, L, Angelicheva, D, King, R.H.M, Thomas, P.K
Published in Neuromuscular disorders : NMD (01.12.2000)
Published in Neuromuscular disorders : NMD (01.12.2000)
Get full text
Journal Article