A citation-based method for searching scientific literature

Fedik Rahimov, Lucilene Arilho Ribeiro, Eziquiel de Miranda, Antonio Richieri-Costa, Jeffrey C Murray. Am J Med Genet A 2006
Times Cited: 43



Kelly A Bear, Benjamin D Solomon, Sonir Antonini, Ivo J P Arnhold, Marcela M França, Erica H Gerkes, Dorothy K Grange, Donald W Hadley, Jarmo Jääskeläinen, Sabrina S Paulo, Patrick Rump, Constantine A Stratakis, Elizabeth M Thompson, Mary Willis, Thomas L Winder, Alexander A L Jorge, Erich Roessler, Maximilian Muenke. J Med Genet 2014
Times Cited: 40




List of shared articles



Times cited


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
29

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
0

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
3

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
5

Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly.
Ariel F Martinez, Paul S Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
3

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
32

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
38

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
85

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
2