A citation-based method for searching scientific literature

E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
Times Cited: 841



Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel, Marion Belleguic, Leslie Ratié, Laurent Pasquier, Philippe Loget, Claude Bendavid, Sylvie Jaillard, Lucie Rochard, Chloé Quélin, Valérie Dupé, Véronique David, Sylvie Odent. J Med Genet 2011
Times Cited: 76




List of shared articles



Times cited

Cilia, ciliopathies and hedgehog-related forebrain developmental disorders.
Abraham Andreu-Cervera, Martin Catala, Sylvie Schneider-Maunoury. Neurobiol Dis 2021
1

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

Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specific.
Cedrik Tekendo-Ngongang, Babajide Owosela, Maximilian Muenke, Paul Kruszka. Am J Med Genet C Semin Med Genet 2020
2

Developmental Genes and Malformations in the Hypothalamus.
Carmen Diaz, Luis Puelles. Front Neuroanat 2020
2

Nasal fistula, epidermal cyst and hypernatremia in a girl presenting holoprosencephaly due to a rare ZIC2 point mutation.
Ivan Gonçalves de Almeida, Daniel Kanami Kuratani, Letícia Machado Gomes, Marilu Fiegenbaum, Elisa Pacheco Estima Correia, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa. Eur J Med Genet 2020
0

Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
Artem Kim, Clara Savary, Christèle Dubourg, Wilfrid Carré, Charlotte Mouden, Houda Hamdi-Rozé, Hélène Guyodo, Jerome Le Douce, Laurent Pasquier, Elisabeth Flori,[...]. Brain 2019
21

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

Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in Germany.
Sophie Hinreiner, Dagmar Wieczorek, Dietmar Mueller, Tanja Roedl, Gundula Thiel, Ute Grasshoff, Rabih Chaoui, Ute Hehr. Am J Med Genet C Semin Med Genet 2018
1

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

Recent advances in understanding inheritance of holoprosencephaly.
Christèle Dubourg, Artem Kim, Erwan Watrin, Marie de Tayrac, Sylvie Odent, Véronique David, Valérie Dupé. Am J Med Genet C Semin Med Genet 2018
21

Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing.
C Mouden, C Dubourg, W Carré, S Rose, C Quelin, L Akloul, H Hamdi-Rozé, G Viot, H Salhi, P Darnault,[...]. Clin Genet 2016
27