A citation-based method for searching scientific literature

Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
Times Cited: 62



F Lacbawan, B D Solomon, E Roessler, K El-Jaick, S Domené, J I Vélez, N Zhou, D Hadley, J Z Balog, R Long, A Fryer, W Smith, S Omar, S D McLean, K Clarkson, A Lichty, N J Clegg, M R Delgado, E Levey, E Stashinko, L Potocki, M I Vanallen, J Clayton-Smith, D Donnai, D W Bianchi, P B Juliusson, P R Njølstad, H G Brunner, J C Carey, U Hehr, J Müsebeck, P F Wieacker, A Postra, R C M Hennekam, M-J H van den Boogaard, A van Haeringen, A Paulussen, J Herbergs, C T R M Schrander-Stumpel, A R Janecke, D Chitayat, J Hahn, D M McDonald-McGinn, E H Zackai, W B Dobyns, M Muenke. J Med Genet 2009
Times Cited: 65




List of shared articles



Times cited

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel, Marion Belleguic, Leslie Ratié, Laurent Pasquier, Philippe Loget, Claude Bendavid,[...]. J Med Genet 2011
76

Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.
Christina Tatsi, Amalia Sertedaki, Antonis Voutetakis, Eleni Valavani, Maria-Alexandra Magiakou, Christina Kanaka-Gantenbein, George P Chrousos, Catherine Dacou-Voutetakis. J Clin Endocrinol Metab 2013
35

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

Holoprosencephaly: a guide to diagnosis and clinical management.
Manu S Raam, Benjamin D Solomon, Maximilian Muenke. Indian Pediatr 2011
22

Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses.
F Petracchi, L Crespo, C Michia, L Igarzabal, E Gadow. Prenat Diagn 2011
11

ZIC2 in Holoprosencephaly.
Kristen S Barratt, Ruth M Arkell. Adv Exp Med Biol 2018
7

Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly.
Emily F Kauvar, Ping Hu, Daniel E Pineda-Alvarez, Benjamin D Solomon, Amalia Dutra, Evgenia Pak, Brooke Blessing, Virginia Proud, Alan L Shanske, Cathy A Stevens,[...]. Mol Genet Metab 2011
9

Holoprosencephaly: recommendations for diagnosis and management.
Emily F Kauvar, Maximilian Muenke. Curr Opin Pediatr 2010
28


New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly.
Viviane Freitas de Castro, Daniel Mattos, Flavia Martinez de Carvalho, Denise Pontes Cavalcanti, Milagros M Duenas-Roque, Juan Llerena, Viviana Raquel Cosentino, Rachel Sayuri Honjo, Julio Cesar Loguercio Leite, Maria Teresa Sanseverino,[...]. Mol Syndromol 2021
0