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Published in BMC genomics (21.03.2011)
Published in BMC genomics (21.03.2011)
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Angiopoietin-1 is required for Schlemm's canal development in mice and humans
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Use of schizophrenia and bipolar disorder polygenic risk scores to identify psychotic disorders
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Published in British journal of psychiatry (01.09.2018)
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A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains
Ranlund, Siri, Calafato, Stella, Thygesen, Johan H., Lin, Kuang, Cahn, Wiepke, Crespo‐Facorro, Benedicto, de Zwarte, Sonja M.C., Díez, Álvaro, Di Forti, Marta, Iyegbe, Conrad, Jablensky, Assen, Jones, Rebecca, Hall, Mei‐Hua, Kahn, Rene, Kalaydjieva, Luba, Kravariti, Eugenia, McDonald, Colm, McIntosh, Andrew M., McQuillin, Andrew, Picchioni, Marco, Prata, Diana P., Rujescu, Dan, Schulze, Katja, Shaikh, Madiha, Toulopoulou, Timothea, van Haren, Neeltje, van Os, Jim, Vassos, Evangelos, Walshe, Muriel, Lewis, Cathryn, Murray, Robin M., Powell, John, Bramon, Elvira
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2018)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2018)
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Null Mutations in LTBP2 Cause Primary Congenital Glaucoma
Ali, Manir, McKibbin, Martin, Booth, Adam, Parry, David A., Jain, Payal, Riazuddin, S. Amer, Hejtmancik, J. Fielding, Khan, Shaheen N., Firasat, Sabika, Shires, Mike, Gilmour, David F., Towns, Katherine, Murphy, Anna-Louise, Azmanov, Dimitar, Tournev, Ivailo, Cherninkova, Sylvia, Jafri, Hussain, Raashid, Yasmin, Toomes, Carmel, Craig, Jamie, Mackey, David A., Kalaydjieva, Luba, Riazuddin, Sheikh, Inglehearn, Chris F.
Published in American journal of human genetics (15.05.2009)
Published in American journal of human genetics (15.05.2009)
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Functionally distinct PI 3-kinase pathways regulate myelination in the peripheral nervous system
Heller, Bradley A, Ghidinelli, Monica, Voelkl, Jakob, Einheber, Steven, Smith, Ryan, Grund, Ethan, Morahan, Grant, Chandler, David, Kalaydjieva, Luba, Giancotti, Filippo, King, Rosalind H, Fejes-Toth, Aniko Naray, Fejes-Toth, Gerard, Feltri, Maria Laura, Lang, Florian, Salzer, James L
Published in The Journal of cell biology (31.03.2014)
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Origins, admixture and founder lineages in European Roma
Martínez-Cruz, Begoña, Mendizabal, Isabel, Harmant, Christine, de Pablo, Rosario, Ioana, Mihai, Angelicheva, Dora, Kouvatsi, Anastasia, Makukh, Halyna, Netea, Mihai G, Pamjav, Horolma, Zalán, Andrea, Tournev, Ivailo, Marushiakova, Elena, Popov, Vesselin, Bertranpetit, Jaume, Kalaydjieva, Luba, Quintana-Murci, Lluis, Comas, David
Published in European journal of human genetics : EJHG (01.06.2016)
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Deleterious GRM1 mutations in schizophrenia
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Published in PloS one (20.03.2012)
Published in PloS one (20.03.2012)
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ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies
Chamova, Teodora, Florez, Laura, Guergueltcheva, Velina, Raycheva, Margarita, Kaneva, Radka, Lochmüller, Hanns, Kalaydjieva, Luba, Tournev, Ivailo
Published in Journal of neurology (01.05.2012)
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LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population
AZMANOV, Dimitar N, DIMITROVA, Stanislava, SOODYALL, Himla, CHAKRABARTI, Subhabrata, PADH, Harish, LOPEZ-NEVOT, Miguel A, CHERNODRINSKA, Violeta, ANGUELOV, Botio, MAJUMDER, Partha, ANGELOVA, Lyudmila, KANEVA, Radka, MACKEY, David A, FLOREZ, Laura, TOURNEV, Ivailo, KALAYDJIEVA, Luba, CHERNINKOVA, Sylvia, DRAGANOV, Dragomir, MORAR, Bharti, SAAT, Rosmawati, JUAN, Manel, AROSTEGUI, Juan I, GANGULY, Sriparna
Published in European journal of human genetics : EJHG (01.03.2011)
Published in European journal of human genetics : EJHG (01.03.2011)
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Ndrg1 in development and maintenance of the myelin sheath
King, Rosalind H.M, Chandler, David, Lopaticki, Sash, Huang, Dexing, Blake, Julian, Muddle, John R, Kilpatrick, Trevor, Nourallah, Michelle, Miyata, Toshiyuki, Okuda, Tomohiko, Carter, Kim W, Hunter, Michael, Angelicheva, Dora, Morahan, Grant, Kalaydjieva, Luba
Published in Neurobiology of disease (01.06.2011)
Published in Neurobiology of disease (01.06.2011)
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N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom
Kalaydjieva, Luba, Gresham, David, Gooding, Rebecca, Heather, Lisa, Baas, Frank, de Jonge, Rosalein, Blechschmidt, Karin, Angelicheva, Dora, Chandler, David, Worsley, Penelope, Rosenthal, Andre, King, Rosalind H.M., Thomas, P.K.
Published in American journal of human genetics (01.07.2000)
Published in American journal of human genetics (01.07.2000)
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Cognitive Impairment and Brain Imaging Characteristics of Patients with Congenital Cataracts, Facial Dysmorphism, Neuropathy Syndrome
Kalaydjieva, Luba, Bichev, Stoyan, Raycheva, Margarita, Zlatareva, Dora, Chamova, Teodora, Tournev, Ivailo
Published in Behavioural neurology (01.01.2015)
Published in Behavioural neurology (01.01.2015)
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Impact of the Reelin signaling cascade (Ligands-Receptors-Adaptor Complex) on cognition in schizophrenia
Verbrugghe, Phebe, Bouwer, Sonja, Wiltshire, Steven, Carter, Kim, Chandler, David, Cooper, Matthew, Morar, Bharti, Razif, Muhammad F.M., Henders, Anjali, Badcock, Johanna C., Dragovic, Milan, Carr, Vaughan, Almeida, Osvaldo P., Flicker, Leon, Montgomery, Grant, Jablensky, Assen, Kalaydjieva, Luba
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2012)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2012)
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Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes
Stephens, J. Claiborne, Reich, David E., Goldstein, David B., Shin, Hyoung Doo, Smith, Michael W., Carrington, Mary, Winkler, Cheryl, Huttley, Gavin A., Allikmets, Rando, Schriml, Lynn, Gerrard, Bernard, Malasky, Michael, Ramos, Maria D., Morlot, Susanne, Tzetis, Maria, Oddoux, Carole, di Giovine, Francesco S., Nasioulas, Georgios, Chandler, David, Aseev, Michael, Hanson, Matthew, Kalaydjieva, Luba, Glavac, Damjan, Gasparini, Paolo, Kanavakis, E., Claustres, Mireille, Kambouris, Marios, Ostrer, Harry, Duff, Gordon, Baranov, Vladislav, Sibul, Hiljar, Metspalu, Andres, Goldman, David, Martin, Nick, Duffy, David, Schmidtke, Jorg, Estivill, Xavier, O'Brien, Stephen J., Dean, Michael
Published in American journal of human genetics (01.06.1998)
Published in American journal of human genetics (01.06.1998)
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Y-chromosome analysis in individuals bearing the Basarab name of the first dynasty of Wallachian kings
Martinez-Cruz, Begoña, Ioana, Mihai, Calafell, Francesc, Arauna, Lara R, Sanz, Paula, Ionescu, Ramona, Boengiu, Sandu, Kalaydjieva, Luba, Pamjav, Horolma, Makukh, Halyna, Plantinga, Theo, van der Meer, Jos W M, Comas, David, Netea, Mihai G
Published in PloS one (25.07.2012)
Published in PloS one (25.07.2012)
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Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX
May, Celia A, Shone, Angela C, Kalaydjieva, Luba, Sajantila, Antti, Jeffreys, Alec J
Published in Nature genetics (01.07.2002)
Published in Nature genetics (01.07.2002)
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