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Times Cited: 43
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List of shared articles
Times cited
A case series of a mother and two daughters with a GLI2 gene deletion demonstrating variable expressivity and incomplete penetrance.
Cameron Elward, Janet Berg, John M Oberlin, Luis Rohena. Clin Case Rep 2020
Cameron Elward, Janet Berg, John M Oberlin, Luis Rohena. Clin Case Rep 2020
Gli2 gene-environment interactions contribute to the etiological complexity of holoprosencephaly: evidence from a mouse model.
Galen W Heyne, Joshua L Everson, Lydia J Ansen-Wilson, Cal G Melberg, Dustin M Fink, Kia F Parins, Padydeh Doroodchi, Caden M Ulschmid, Robert J Lipinski. Dis Model Mech 2016
Galen W Heyne, Joshua L Everson, Lydia J Ansen-Wilson, Cal G Melberg, Dustin M Fink, Kia F Parins, Padydeh Doroodchi, Caden M Ulschmid, Robert J Lipinski. Dis Model Mech 2016
Truncating and zinc-finger variants in GLI2 are associated with hypopituitarism.
Megan L Corder, Siren Berland, Jostein A Førsvoll, Indraneel Banerjee, Phil Murray, Eirik Bratland, David Gokhale, Gunnar Houge, Sofia Douzgou. Am J Med Genet A 2022
Megan L Corder, Siren Berland, Jostein A Førsvoll, Indraneel Banerjee, Phil Murray, Eirik Bratland, David Gokhale, Gunnar Houge, Sofia Douzgou. Am J Med Genet A 2022
Two novel heterozygous missense variations within the GLI2 gene in two unrelated Argentine patients.
Matías Juanes, Isabel Di Palma, Marta Ciaccio, Roxana Marino, Pablo C Ramírez, Natalia Pérez Garrid, Mercedes Maceiras, Juan M Lazzati, Marco A Rivarola, Alicia Belgorosky. Medicina (B Aires) 2016
Matías Juanes, Isabel Di Palma, Marta Ciaccio, Roxana Marino, Pablo C Ramírez, Natalia Pérez Garrid, Mercedes Maceiras, Juan M Lazzati, Marco A Rivarola, Alicia Belgorosky. Medicina (B Aires) 2016
A novel truncating variant of GLI2 associated with Culler-Jones syndrome impairs Hedgehog signalling.
Fabiola Valenza, Davide Cittaro, Elia Stupka, Donatella Biancolini, Maria Grazia Patricelli, Dario Bonanomi, Dejan Lazarević. PLoS One 2019
Fabiola Valenza, Davide Cittaro, Elia Stupka, Donatella Biancolini, Maria Grazia Patricelli, Dario Bonanomi, Dejan Lazarević. PLoS One 2019
Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly.
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
Role of GLI Transcription Factors in Pathogenesis and Their Potential as New Therapeutic Targets.
Maja Sabol, Diana Trnski, Vesna Musani, Petar Ozretić, Sonja Levanat. Int J Mol Sci 2018
Maja Sabol, Diana Trnski, Vesna Musani, Petar Ozretić, Sonja Levanat. Int J Mol Sci 2018
Role of GLI2 in hypopituitarism phenotype.
Ivo J P Arnhold, Marcela M França, Luciani R Carvalho, Berenice B Mendonca, Alexander A L Jorge. J Mol Endocrinol 2015
Ivo J P Arnhold, Marcela M França, Luciani R Carvalho, Berenice B Mendonca, Alexander A L Jorge. J Mol Endocrinol 2015
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
Qing Fang, Akima S George, Michelle L Brinkmeier, Amanda H Mortensen, Peter Gergics, Leonard Y M Cheung, Alexandre Z Daly, Adnan Ajmal, María Ines Pérez Millán, A Bilge Ozel,[...]. Endocr Rev 2016
Qing Fang, Akima S George, Michelle L Brinkmeier, Amanda H Mortensen, Peter Gergics, Leonard Y M Cheung, Alexandre Z Daly, Adnan Ajmal, María Ines Pérez Millán, A Bilge Ozel,[...]. Endocr Rev 2016
Unique near-complete deletion of GLI2 in a patient with combined pituitary hormone deficiency and post-axial polydactyly.
Melitza S M Elizabeth, Annemieke J M H Verkerk, Anita C S Hokken-Koelega, Joost A M Verlouw, Jesús Argente, Roland Pfaeffle, Theo J Visser, Robin P Peeters, Laura C G De Graaff. Growth Horm IGF Res 2020
Melitza S M Elizabeth, Annemieke J M H Verkerk, Anita C S Hokken-Koelega, Joost A M Verlouw, Jesús Argente, Roland Pfaeffle, Theo J Visser, Robin P Peeters, Laura C G De Graaff. Growth Horm IGF Res 2020