Carlos David Bruque (Carlos D Bruque)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 13

Top Venues

National Center for Medical Genetics - ANLIS-Malbrán

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

Affiliation History

National Center for Medical Genetics - ANLIS-Malbrán Apr 15 2015

Argentina

Professional Health Assistance :: Department of Diagnostic

Publications

Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natalia García-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg, Susanna Balcells
Evolutionary and functional analyses of LRP5 in archaic and extant modern humans. Human genomics 18 (1) (2024)
Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natalia García-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg, Susanna Balcells
Evolutionary and functional analyses of LRP5 in archaic and extant modern humans. Human genomics 18 (1) (2024)
Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natalia García-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg, Susanna Balcells
Evolutionary and functional analyses of LRP5 in archaic and extant modern humans. Human genomics 18 (1) (2024)
Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natalia García-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg, Susanna Balcells
Evolutionary and functional analyses of LRP5 in archaic and extant modern humans. Human genomics 18 (1) (2024)
Martina Jabloñski, María Sol Rodríguez, Ezequiel Mariano Rivero, Carlos David Bruque, Silvia Vanzulli, Ariana Bruzzone, Cecilia Pérez Piñero, Isabel Alicia Lüthy
The Beta2-adrenergic agonist salbutamol synergizes with paclitaxel on cell proliferation and tumor growth in triple negative breast cancer models. Cancer chemotherapy and pharmacology (2023)
Núria Martínez-Gil, Diana Ovejero, Natalia García-Giralt, Carlos David Bruque, Leonardo Mellibovsky, Xavier Nogués, Raquel Rabionet, Daniel Grinberg, Susanna Balcells
Genetic Analysis in a Familial Case With High Bone Mineral Density Suggests Additive Effects at Two Loci. JBMR plus 6 (4) (2022)
Paula I Buonfiglio, Carlos David Bruque, Vanesa Lotersztein, Leonela Luce, Florencia Giliberto, Sebastián Menazzi, Liliana Francipane, Bibiana Paoli, Ernesto Goldschmidt, Ana Belén Elgoyhen, Viviana Dalamón
Predicting pathogenicity for novel hearing loss mutations based on genetic and protein structure approaches. Scientific reports 12 (1) (2022)
Marisol Delea, Lucia S Massara, Lucia D Espeche, María Paz Bidondo, Pablo Barbero, Jaen Oliveri, Paloma Brun, Mónica Fabro, Micaela Galain, Cecilia S Fernández, Melisa Taboas, Carlos David Bruque, Jorge E Kolomenski, Agustín Izquierdo, Ariel Berenstein, Viviana Cosentino, Celeste Martinoli, Mariana Vilas, Mónica Rittler, Hector R Mendez, Lilian Furforo, Rosa Liascovich, Boris Groisman, Sandra Rozental, Liliana Beatriz Dain, null On Behalf Of The Pid Acm-Cc Group
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease. Genes 13 (7) (2022)
Cecilia S Fernández, Melisa Taboas, Carlos David Bruque, Belén Benavides-Mori, Susana Belli, Mirta Stivel, Adriana Oneto, Titania Pasqualini, Marisol Delea, Lucía Daniela Espeche, Jorge E Kolomenski, Liliana Alba, Noemí Buzzalino, Liliana Beatriz Dain
Genetic characterization of a large cohort of Argentine 21-hydroxylase Deficiency. Clinical endocrinology 93 (1) (2020)
Jorge E Kolomenski, Marisol Delea, Leandro Simonetti, Mónica C Fabbro, Lucía Daniela Espeche, Melisa Taboas, Alejandro Daniel Nadra, Carlos David Bruque, Liliana Beatriz Dain
An update on genetic variants of the NKX2-5. Human mutation 41 (7) (2020)
Paula I Buonfiglio, Carlos David Bruque, Leonela Luce, Florencia Giliberto, Vanesa Lotersztein, Sebastián Menazzi, Bibiana Paoli, Ana Belén Elgoyhen, Viviana Dalamón
GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort. Genes 11 (10) (2020)
Marisol Delea, Lucía D Espeche, Carlos David Bruque, María Paz Bidondo, Lucía S Massara, Jaen Oliveri, Paloma Brun, Viviana R Cosentino, Celeste Martinoli, Norma Tolaba, Claudina Picon, María Eugenia Ponce Zaldua, Silvia Ávila, Viviana Gutnisky, Myriam Perez, Lilian Furforo, Noemí D Buzzalino, Rosa Liascovich, Boris Groisman, Mónica Rittler, Sandra Rozental, Pablo Barbero, Liliana Dain
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects. Genes 9 (9) (2018)
Leandro Simonetti, Carlos David Bruque, Cecilia S Fernández, Belén Benavides-Mori, Marisol Delea, Jorge E Kolomenski, Lucía D Espeche, Noemí D Buzzalino, Alejandro D Nadra, Liliana Beatriz Dain
CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants. Human mutation 39 (1) (2017)

Carlos David Bruque.css-eqlu8i{font-size:small;padding-left:4px;} (Carlos D Bruque)

Publication Activity (10 Years)

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Top Venues

Carlos David Bruque (Carlos D Bruque)