A citation-based method for searching scientific literature




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 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

In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics.
Karin Weiss, Paul Kruszka, Maria J Guillen Sacoto, Yonit A Addissie, Donald W Hadley, Casey K Hadsall, Bethany Stokes, Ping Hu, Erich Roessler, Beth Solomon,[...]. Genet Med 2018
11

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

Cyclopia: isolated and with agnathia-otocephaly complex.
Lin Tun Wai, Suresh Chandran. BMJ Case Rep 2017
6

Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene.
Clarice Pagani Savastano, Pricila Bernardi, Hector N Seuánez, Miguel Ângelo Martins Moreira, Iêda Maria Orioli. Birth Defects Res A Clin Mol Teratol 2014
5

Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH.
Daniel E Pineda-Alvarez, Erich Roessler, Ping Hu, Kshitij Srivastava, Benjamin D Solomon, C Evan Siple, Chen-Ming Fan, Maximilian Muenke. Hum Genet 2012
39