Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease by Kristina Grigalionienė, Birutė Burnytė, Laima Ambrozaitytė, Algirdas Utkus

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Kearns‐Sayre syndrome case. Novel 5,9 kb mtDNA deletion by Kristina Grigalionienė, Birutė Burnytė, Danutė Balkelienė, Laima Ambrozaitytė, Algirdas Utkus

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X-linked juvenile retinoschisis: phenotypic and genetic characterization by Rasa Strupaitė, Laima Ambrozaitytė, Loreta Cimbalistienė, Rimvydas Ašoklis, Algirdas Utkus

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Diagnostic Significance of FNAB miRNA Expression in Papillary Thyroid Carcinoma by Romena Laukienė, Laima Ambrozaityte, Loreta Cimbalistienė, Algirdas Utkus, Algirdas Edvardas Tamosiunas

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Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort by Karolis Baronas, Tautvydas Rančelis, Aidas Pranculis, Ingrida Domarkienė, Laima Ambrozaitytė, Vaidutis Kučinskas

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Identifying Genomic Signatures of Positive Selection to Predict Protective Genomic Loci in the Cohort of Lithuanian Clean-Up Workers of the Chornobyl Nuclear Disaster by Gabrielė Žukauskaitė, Ingrida Domarkienė, Aušra Matulevičienė, Svetlana Dauengauer-Kirlienė, Vaidutis Kučinskas, Laima Ambrozaitytė

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Putative protective genomic variation in the Lithuanian population by Gabrielė Žukauskaitė, Ingrida Domarkienė, Tautvydas Rančelis, Ingrida Kavaliauskienė, Karolis Baronas, Vaidutis Kučinskas, Laima Ambrozaitytė

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Psychological distress 35 years after the Chornobyl accident in the Lithuanian clean-up workers by Evaldas Kazlauskas, Giedre Smailyte, Ingrida Domarkienė, Vaidutis Kučinskas, Aušra Matulevičienė, Ask Elklit, Gabrielė Žukauskaitė, Laima Ambrozaitytė

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Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies by Eglė Preikšaitienė, Laima Ambrozaitytė, Živilė Maldžienė, Aušra Morkūnienė, Loreta Cimbalistienė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas

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Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in <i>MED13L</i> Haploinsufficiency Syndrome by Evelina Siavrienė, Gunda Petraitytė, Violeta Mikštienė, Živilė Maldžienė, Aušra Sasnauskienė, Vilmantė Žitkutė, Laima Ambrozaitytė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė

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CyberGenomics: Application of Behavioral Genetics in Cybersecurity by Ingrida Domarkienė, Laima Ambrozaitytė, Linas Bukauskas, Tautvydas Rančelis, Stefan Sütterlin, Benjamin James Knox, Kaie Maennel, Olaf Maennel, Karen Parish, Ricardo Gregorio Lugo, Agnė Brilingaitė

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Donor Splice Site Variant in <i>SLC9A6</i> Causes Christianson Syndrome in a Lithuanian Family: A Case Report by Gunda Petraitytė, Violeta Mikštienė, Evelina Siavrienė, Loreta Cimbalistienė, Živilė Maldžienė, Tautvydas Rančelis, Evelina Marija Vaitėnienė, Laima Ambrozaitytė, Justas Dapkūnas, Ramūnas Dzindzalieta, Erinija Pranckevičienė, Vaidutis Kučinskas, Algirdas Utkus, Eglė Preikšaitienė

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Higher levels of plasma Adrenocorticotropic hormone (ACTH) are associated with lower suicidal ideation in depressed patients compared to controls and suicide attempters, independen... by Robertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, Robertas Badaras, Edgaras Dlugauskas, Sigita Lesinskiene, Eimantas Matiekus, Martynas Marcinkevicius, Lina Venceviciene, Algirdas Utkus, Andrius Kaminskas, Tomas Petrenas, Jurgita Songailiene, Dalius Vitkus, Laima Ambrozaityte

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One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome by Robert Meyer, Matthias Begemann, Christian Thomas Hübner, Daniela Dey, Alma Kuechler, Magdeldin Elgizouli, Ulrike Schara, Laima Ambrozaityte, Birute Burnyte, Carmen Schröder, Asmaa Kenawy, Peter Kroisel, Stephanie Demuth, Gyorgy Fekete, Thomas Opladen, Miriam Elbracht, Thomas Eggermann

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HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling by Matilde Malcorps, Silvia Amor-Barris, Birute Burnyte, Ramune Vilimiene, Camila Armirola-Ricaurte, Kristina Grigalioniene, Alexandra Ekshteyn, Ausra Morkuniene, Arunas Vaitkevicius, Els De Vriendt, Jonathan Baets, Steven S. Scherer, Laima Ambrozaityte, Algirdas Utkus, Albena Jordanova, Kristien Peeters

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Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis by Deborah J. G. Mackay, Gabriella Gazdagh, David Monk, Frederic Brioude, Eloise Giabicani, Izabela M. Krzyzewska, Jennifer M. Kalish, Saskia M. Maas, Masayo Kagami, Jasmin Beygo, Tiina Kahre, Jair Tenorio-Castano, Laima Ambrozaitytė, Birutė Burnytė, Flavia Cerrato, Justin H. Davies, Giovanni Battista Ferrero, Olga Fjodorova, Africa Manero-Azua, Arrate Pereda, Silvia Russo, Pierpaola Tannorella, Karen I. Temple, Katrin Õunap, Andrea Riccio, Guiomar Perez de Nanclares, Eamonn R. Maher, Pablo Lapunzina, Irène Netchine, Thomas Eggermann, Jet Bliek, Zeynep Tümer

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