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



E Matsunaga, K Shiota. Teratology 1977
Times Cited: 236




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

Nationwide epidemiological survey of holoprosencephaly in Japan.
Yuichi Abe, Ryuichiro Araki, Hisanori Sobajima, Masanori Tamura, Tetsuya Kunikata, Akira Ohtake, Hideo Yamanouchi. Pediatr Int 2020
0

Developmental Toxicity Assessment of Piperonyl Butoxide Exposure Targeting Sonic Hedgehog Signaling and Forebrain and Face Morphogenesis in the Mouse: An in Vitro and in Vivo Study.
Joshua L Everson, Miranda R Sun, Dustin M Fink, Galen W Heyne, Cal G Melberg, Kia F Nelson, Padydeh Doroodchi, Lydia J Colopy, Caden M Ulschmid, Alexander A Martin,[...]. Environ Health Perspect 2019
11

Congenital eye anomalies: More mosaic than thought?
Hideyo Ohuchi, Keita Sato, Munenori Habuta, Hirofumi Fujita, Tetsuya Bando. Congenit Anom (Kyoto) 2019
4

Loss-of-function mutations in FGF8 can be independent risk factors for holoprosencephaly.
Sungkook Hong, Ping Hu, Erich Roessler, Tommy Hu, Maximilian Muenke. Hum Mol Genet 2018
11

Clinical and Demographic Evaluation of a Holoprosencephaly Cohort From the Kyoto Collection of Human Embryos.
Yu Abe, Paul Kruszka, Ariel F Martinez, Erich Roessler, Kohei Shiota, Shigehito Yamada, Maximilian Muenke. Anat Rec (Hoboken) 2018
7

Holoprosencephaly in the genomics era.
Erich Roessler, Ping Hu, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
22

Subtle Changes in the Levels of BCL-2 Proteins Cause Severe Craniofacial Abnormalities.
Stephanie Grabow, Andrew J Kueh, Francine Ke, Hannah K Vanyai, Bilal N Sheikh, Michael A Dengler, William Chiang, Samantha Eccles, Ian M Smyth, Lynelle K Jones,[...]. Cell Rep 2018
18

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

Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly.
Tommy Hu, Paul Kruszka, Ariel F Martinez, Jeffrey E Ming, Emily K Shabason, Manu S Raam, Tamim H Shaikh, Daniel E Pineda-Alvarez, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
2

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
25