Juliana Lores

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Venues

Arquivos brasileiros de cardiologia

Pharmacogenomics and personalized medicine

American journal of medical genetics. Part C, Seminars in medical genetics

European journal of human genetics : EJHG

Fundacion Valle del Lili

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

Affiliation History

Fundacion Valle del Lili Nov 15 2018

Colombia

Médica hospitalaria, asistente en i :: Centro de Investigaciones Clínicas

Publications

Ana M. Aristizabal, Carlos Alberto Guzmán-Serrano, María Isabel Lizcano, Walter Mosquera, Juliana Lores, Harry Pachajoa, Cesar Cely
FLNC Associated Restrictive Cardiomyopathy and Hypertrabeculation, a Rare Association. Arquivos brasileiros de cardiologia 121 (5) (2024)
Ana M. Aristizabal, Carlos Alberto Guzmán-Serrano, María Isabel Lizcano, Walter Mosquera, Juliana Lores, Harry Pachajoa, Cesar Cely
FLNC Associated Restrictive Cardiomyopathy and Hypertrabeculation, a Rare Association. Arquivos brasileiros de cardiologia 121 (5) (2024)
Harry Pachajoa, Eidith Gomez-Pineda, Sebastian Giraldo-Ocampo, Juliana Lores
Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies. Pharmacogenomics and personalized medicine 15 (2022)
Lina Perafan-Valdes, Sebastian Giraldo-Ocampo, Juliana Lores, Harry Pachajoa
Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1 . Pharmacogenomics and personalized medicine 15 (2022)
Gabriel David Pinilla-Monsalve, Juliana Lores, Harry Pachajoa, Juan D López-Ponce de León, Alejandro López, Lisa X Rodríguez-Rojas, José Antonio Nastasi-Catanese
A Novel APOC2 Mutation in a Colombian Patient with Recurrent Hypertriglyceridemic Pancreatitis. The application of clinical genetics 13 (2020)
Malena Daich Varela, Rene Moya, Patricio G Schlottmann, Robert B Hufnagel, Claudia Arberas, Federico M Fernández, M Eugenia Inga, Juliana Lores, Harry Pachajoa, Carlos E Prada, Juliana M Ferraz Sallum
Ophthalmic genetics in South America. American journal of medical genetics. Part C, Seminars in medical genetics 184 (3) (2020)
Juliana Lores, Carlos E Prada, Diana Ramírez-Montaño, José A Nastasi-Catanese, Harry Pachajoa
Clinical and molecular analysis of 26 individuals with Noonan syndrome in a reference institution in Colombia. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)
Nina McTiernan, Harinder Gill, Carlos E Prada, Harry Pachajoa, Juliana Lores, null null, Thomas Arnesen
NAA10 p.(N101K) disrupts N-terminal acetyltransferase complex NatA and is associated with developmental delay and hemihypertrophy. European journal of human genetics : EJHG 29 (2) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Juliana Lores