Janet Hoenicka

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 12

Top Venues

Annals of clinical and translational neurology

Movement disorders : official journal of the Movement Disorder Society

International journal of molecular sciences

Journal of clinical medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Daniel Natera-de Benito, Jonathan Olival, Carla Garcia-Cabau, Cristina Jou, Mònica Roldan, Anna Codina, Jessica Expósito-Escudero, Cristina Batlle, Laura Carrera-García, Carlos Ortez, Xavier Salvatella, Francesc Palau, Andrés Nascimento, Janet Hoenicka
Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of clinical and translational neurology (2023)
Jordi Pijuan, Irina F Sevrioukova, Óscar García-Campos, Mar Hernaez, Laura Gort, Marta Gómez-Chiari, Cristina Jou, Santiago Candela-Cantó, Jordi Rumiá, Rafael Artuch, Francesc Palau, Janet Hoenicka, Juan Dario Ortigoza-Escobar
A Novel AIFM1-Related Disorder Phenotype Treated with Deep Brain Stimulation. Movement disorders : official journal of the Movement Disorder Society (2023)
Lara Cantarero, Gisela García-Vargas, Janet Hoenicka, Francesc Palau
Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites. Biology open (2023)
Daniel Natera-de Benito, Jonathan Olival, Carla Garcia-Cabau, Cristina Jou, Mònica Roldan, Anna Codina, Jessica Expósito-Escudero, Cristina Batlle, Laura Carrera-García, Carlos Ortez, Xavier Salvatella, Francesc Palau, Andrés Nascimento, Janet Hoenicka
Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of clinical and translational neurology 10 (3) (2023)
Daniel Natera-de Benito, Jonathan Olival, Carla Garcia-Cabau, Cristina Jou, Mònica Roldan, Anna Codina, Jessica Expósito-Escudero, Cristina Batlle, Laura Carrera-García, Carlos Ortez, Xavier Salvatella, Francesc Palau, Andrés Nascimento, Janet Hoenicka
Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of clinical and translational neurology 10 (3) (2023)
Lydia Vela, Daniele Urso, Mireia Osuna Lopez, Janet Hoenicka
Non-Motor Symptoms in PLA2G6- Associated Dystonia-Parkinsonism: A Case Report and Literature Review. Journal of clinical medicine 11 (6) (2022)
Cristina Nuevo-Tapioles, Fulvio Santacatterina, Brenda Sánchez-Garrido, Cristina Núñez de Arenas, Adrián Robledo-Bérgamo, Paula Martínez-Valero, Lara Cantarero, Beatriz Pardo, Janet Hoenicka, Michael P Murphy, Jorgina Satrústegui, Francesc Palau, José M Cuezva
Effective therapeutic strategies in a preclinical mouse model of Charcot-Marie-Tooth disease. Human molecular genetics 30 (24) (2022)
Charlotte von der Lippe, Kristian Tveten, Trine E Prescott, Øystein L Holla, Øyvind L Busk, Katherine B Burke, Francis H Sansbury, Júlia Baptista, Andrew E Fry, Derek Lim, Stephen R A Jolles, Jennifer Evans, Deborah Osio, Carol Macmillan, Irene Bruno, Flavio Faltera, Salvador Climent, Roser Urreizti, Janet Hoenicka, Francesc Palau, Ana S A Cohen, Kendra Engleman, Dihong Zhou, Shivarajan M Amudhavalli, Médéric Jeanne, Frédérique Bonnet-Brilhault, Jonathan Lévy, Séverine Drunat, Nicolas Derive, Marte G Haug, Wenche Moe Thorstensen
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin. American journal of medical genetics. Part A (2021)
Jordi Pijuan, Juan Dario Ortigoza-Escobar, Juan Ortiz, Adrián Alcalá, María José Calvo, Mariona Cubells, Cristina Hernando-Davalillo, Francesc Palau, Janet Hoenicka
PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder. Autism research : official journal of the International Society for Autism Research 14 (6) (2021)
Dèlia Yubero, Daniel Natera-de Benito, Jordi Pijuan, Judith Armstrong, Loreto Martorell, Guerau Fernàndez, Joan Maynou, Cristina Jou, Mònica Roldan, Carlos Ortez, Andrés Nascimento, Janet Hoenicka, Francesc Palau
The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases. International journal of molecular sciences 22 (8) (2021)
Mᵃ Alejandra Koeneke Hoenicka, Guillermo Ponce, Johanna Troya-Balseca, Tomás Palomo, Janet Hoenicka
Ankyrin Repeat and Kinase Domain Containing 1 Gene, and Addiction Vulnerability. International journal of molecular sciences 21 (7) (2020)
Sara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, Cornelis Blauwendraat, Astrid D Adarmes-Gómez, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Dolores Buiza-Rueda, Fátima Carrillo, Mario Carrión-Claro, Pilar Gómez-Garre, Silvia Jesús, Miguel A Labrador-Espinosa, Daniel Macias, Carlota Méndez-Del-Barrio, Teresa Periñán-Tocino, Cristina Tejera-Parrado, Laura Vargas-González, Monica Diez-Fairen, Ignacio Alvarez, Juan Pablo Tartari, Mariateresa Buongiorno, Miquel Aguilar, Ana Gorostidi, Jesús Alberto Bergareche, Elisabet Mondragon, Ana Vinagre-Aragon, Ioana Croitoru, Javier Ruiz-Martínez, Oriol Dols-Icardo, Jaime Kulisevsky, Juan Marín-Lahoz, Javier Pagonabarraga, Berta Pascual-Sedano, Mario Ezquerra, Ana Cámara, Yaroslau Compta, Manel Fernández, Rubén Fernández-Santiago, Esteban Muñoz, Eduard Tolosa, Francesc Valldeoriola, Isabel Gonzalez-Aramburu, Antonio Sanchez Rodriguez, María Sierra, Manuel Menéndez-González, Marta Blazquez, Ciara Garcia, Esther Suarez-San Martin, Pedro García-Ruiz, Juan Carlos Martínez-Castrillo, Lydia Vela, Clara Ruz, Francisco Javier Barrero, Francisco Escamilla-Sevilla, Adolfo Mínguez-Castellanos, Debora Cerdan, Cesar Tabernero, Maria Jose Gomez Heredia, Francisco Perez Errazquin, Manolo Romero-Acebal, Cici Feliz, Jose Luis Lopez-Sendon, Marina Mata, Irene Martínez Torres, Jonggeol Jeffrey Kim, Clifton L Dalgard, null null, Janet Brooks, Sara Saez-Atienzar, J Raphael Gibbs, Rafael Jorda, Juan A Botia, Luis Bonet-Ponce, Karen E Morrison, Carl Clarke, Manuela Tan, Huw Morris, Connor Edsall, Dena Hernandez, Javier Simon-Sanchez, Mike A Nalls, Sonja W Scholz, Adriano Jimenez-Escrig, Jacinto Duarte, Francisco Vives, Raquel Duran, Janet Hoenicka, Victoria Alvarez, Jon Infante, Maria José Marti, Jordi Clarimón, Adolfo López de Munain, Pau Pastor, Pablo Mir, Andrew Singleton, null null
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight. Movement disorders : official journal of the Movement Disorder Society 34 (12) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Janet Hoenicka