Albena Jordanova - Institute of Biophysics, Bulgarian Academy of Sciences

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论文共 261 篇作者统计合作学者相似作者

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Clinical and Genetic Variability among Bulgarian Patients with Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay

Teodora Chamova,Neviana Ivanova,Sylvia Cherninkova,Maya Koleva,Dora Zlatareva,Veneta Bojinova,Kalina Mihova,Martin Georgiev,Dilyan Ferdinandov,Stoyan Bichev,Radka Kaneva,Vanio Mitev,Albena Jordanova,Ivailo Tournev

Molecular Genetics & Genomic Medicineno. 7 (2024)

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IN QUEST FOR MOLECULAR PLAYERS AND DRUG TARGETS FOR AMINOACYL-TRNA SYNTHETASE-ASSOCIATED PERIPHERAL NEUROPATHIES

Laura Morant,Biljana Ermanoska,Ricardo Leitao-Goncalves, Tine Ooms, Maria-Luise Petrovic-Erfurth,Ivy Cuijt, Eline Celis,Matilde Malcorps,Vincent Timmerman,Albena Jordanova

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM (2024): S36-S37

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The GENESIS Database and Tools: A Decade of Discovery in Mendelian Genomics

Matt C. Danzi,Eric Powell,Adriana P. Rebelo,Maike F. Dohrn,Danique Beijer,Sarah Fazal,Isaac R. L. Xu,Jessica Medina,Sitong Chen, Yeisha Arcia de Jesus, Jacquelyn Schatzman,Ray E. Hershberger,Mario Saporta,Jonathan Baets,Marni Falk,David N. Herrmann,Steven S. Scherer,Mary M. Reilly,Andrea Cortese,Wilson Marques, Mario R. Carnejo-Olivas,Oranee Sanmaneechai,Marina L. Kennerson,Albena Jordanova, Thiago Y. T. Silva,Jose Luiz Pedroso,Luca Schierbaum,Darius Ebrahimi-Fakhari,Stojan Peric,Yi-Chung Lee,Matthis Synofzik,Mustafa Tekin,Gianina Ravenscroft, Mike Shy,Nazli Basak,Rebecca Schule,Stephan Zuchner

EXPERIMENTAL NEUROLOGY（2024）

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LONG-READ WHOLE-GENOME SEQUENCING IN PERIPHERAL NEURODEGENERATION: CHALLENGES, INSIGHTS, AND PATHS FORWARD

Ayse Candayan, Lorena Luiza Pires Ramos,Els De Vriendt,Albena Jordanova

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM (2024): S137-S137

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Whole Exome Sequencing in Bulgarian Patients with Late-Onset Hereditary Ataxia Expands the Genetic Diversity of the Disease

Nevyana Ivanova,Kalina Mihova,Teodora Chamova,Stoyan Bichev,Kunka Kamenarova,Darina Kachakova,Martin Georgiev,Radosveta Bozhilova, Ina Dimitrova,Alexey Savov, Ivaylo Tarnev,Albena Jordanova,Radka Kaneva

EUROPEAN JOURNAL OF HUMAN GENETICS（2024）

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Biallelic Variants in ARHGAP19 Cause a Motor-Predominant Neuropathy with Asymmetry and Conduction Slowing

Natalia Dominik,Stephanie Efthymiou,Christopher J Record, Xinyu Miao, Renee Lin, Jevin Parmar,Annarita Scardamaglia,Reza Maroofian,Gabriel Aughey, Abigail Wilson,Simon Lowe,Riccardo Curro,Ricardo P Schnekenberg,Shahryar Alavi, Leif Leclaire, Yi He, Kristina Zhelchenska,Yohanns Bellaiche,Isabelle Gaugue,Mariola Skorupinska,Liedewei Van de Vondel,Sahar Da'as,Valentina Turchetti,Serdal Gungor,Ehsan Ghayoor Karimiani,Camila Armirola Ricaurte,Haluk Topaloglu,Albena Jordanova,Mashaya Zaman,Selina H Banu,Wilson Marques,Pedro Jose Tomaselli,Busra Aynekin,Ali Cansu,Huseyin Per,Ayten Gulec,Javeria Raza Alvi,Tipu Sultan, Arif Khan,Giovanni Zifarelli,Shahnaz Ibrahim,Grazia M.S. Mancini,M. Mahdi Motazacker,Esther Brusse,Vincenzo Lupo,Teresa Sevilla,Seyma Tekgul,Robin Palvadeau,A Nazli Basak,Jonathan Baets,Yesim Parman,Arman Cakar,Rita Horvath,Tobias B Haack,Jan-Hendrik Stahl,Kathrin Grundmann-Hauser,Joohyun Park,Stephan Zuchner,Nigel G Laing,Lindsay Wilson,Alexander M. Rossor,James Polke,Fernanda Barbosa Figueiredo, Andre Luiz Pessoa,Fernando Kok,Antonio Rodrigues Coimbra-Neto,Marcondes C Franca,Yalda Jamshidi,Gianina Ravenscroft,Sherifa Ahmed Hamed,Wendy K. Chung,Daniel P Osborn,Michael Hanna,Andrea Cortese,James E C Jepson,Mary M Reilly,Nathalie Lamarche-Vane,Henry Houlden

crossref（2024）

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LOSS OF HINT1 FUNCTION IMPAIRS ACTIN CYTOSKELETON DYNAMICS

Alexandra Ekshteyn, Silvia Amor Barris,Bob Asselbergh,Albena Jordanova

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM (2024): S19-S19

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Identification and Characterization of Novel Founder Mutations in NDRG1: Refining the Genetic Landscape of Charcot–Marie–Tooth Disease Type 4D in Bulgaria

Derek Atkinson,Teodora Chamova,Ayse Candayan,Kristina Kastreva, Ognian Asenov,Ivan Litvinenko,Alejandro Estrada-Cuzcano,Els De Vriendt, Georgi Kukushev,Ivailo Tournev,Albena Jordanova

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESno. 16 (2024)

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Substrate Specificity Controlled by the Exit Site of Human P4-ATPases, Revealed by De Novo Point Mutations in Neurological Disorders

David C. Calianese,Tomoyasu Noji,Jennifer A. Sullivan,Kelly Schoch,Vandana Shashi,Vanda McNiven, Luiza Lorena Pires Ramos,Albena Jordanova, Judit Karteszi,Hiroshi Ishikita,Shigekazu Nagata

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAno. 44 (2024)

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