A citation-based method for searching scientific literature

Artem Kim, Clara Savary, Christèle Dubourg, Wilfrid Carré, Charlotte Mouden, Houda Hamdi-Rozé, Hélène Guyodo, Jerome Le Douce, Laurent Pasquier, Elisabeth Flori, Marie Gonzales, Claire Bénéteau, Odile Boute, Tania Attié-Bitach, Joelle Roume, Louise Goujon, Linda Akloul, Sylvie Odent, Erwan Watrin, Valérie Dupé, Marie de Tayrac, Véronique David. Brain 2019
Times Cited: 21







List of co-cited articles
166 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
22
47

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
33

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
28

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
23

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
62
23

Holoprosencephaly in the genomics era.
Erich Roessler, Ping Hu, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
24
23

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
23

Cooperation of BMP7 and SHH in the induction of forebrain ventral midline cells by prechordal mesoderm.
J K Dale, C Vesque, T J Lints, T K Sampath, A Furley, J Dodd, M Placzek. Cell 1997
245
19

Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia.
Li Zhao, Solsire E Zevallos, Karine Rizzoti, Yongsu Jeong, Robin Lovell-Badge, Douglas J Epstein. Dev Cell 2012
66
19

Sonic hedgehog lineage in the mouse hypothalamus: from progenitor domains to hypothalamic regions.
Gonzalo Alvarez-Bolado, Fabian A Paul, Sandra Blaess. Neural Dev 2012
64
19

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
19

Molecular testing in holoprosencephaly.
Paul Kruszka, Ariel F Martinez, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
11
36

Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway.
Christèle Dubourg, Wilfrid Carré, Houda Hamdi-Rozé, Charlotte Mouden, Joëlle Roume, Benmansour Abdelmajid, Daniel Amram, Clarisse Baumann, Nicolas Chassaing, Christine Coubes,[...]. Hum Mutat 2016
38
19

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
843
19

STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly.
Naseebullah Kakar, Jamil Ahmad, Deborah J Morris-Rosendahl, Janine Altmüller, Katrin Friedrich, Gotthold Barbi, Peter Nürnberg, Christian Kubisch, William B Dobyns, Guntram Borck. Hum Genet 2015
22
14

Role of neuroepithelial Sonic hedgehog in hypothalamic patterning.
Nora-Emöke Szabó, Tianyu Zhao, Murat Cankaya, Thomas Theil, Xunlei Zhou, Gonzalo Alvarez-Bolado. J Neurosci 2009
79
14

Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus.
Roberta Haddad-Tóvolli, Fabian A Paul, Yuanfeng Zhang, Xunlei Zhou, Thomas Theil, Luis Puelles, Sandra Blaess, Gonzalo Alvarez-Bolado. Front Neuroanat 2015
13
23

A genomic atlas of mouse hypothalamic development.
Tomomi Shimogori, Daniel A Lee, Ana Miranda-Angulo, Yanqin Yang, Hong Wang, Lizhi Jiang, Aya C Yoshida, Ayane Kataoka, Hiromi Mashiko, Marina Avetisyan,[...]. Nat Neurosci 2010
243
14

Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.
Charlotte Mouden, Marie de Tayrac, Christèle Dubourg, Sophie Rose, Wilfrid Carré, Houda Hamdi-Rozé, Marie-Claude Babron, Linda Akloul, Bénédicte Héron-Longe, Sylvie Odent,[...]. PLoS One 2015
19
15

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.
M Ishida, T Cullup, C Boustred, C James, J Docker, C English, N Lench, A J Copp, G E Moore, N D E Greene,[...]. Clin Genet 2018
14
21

Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Jennifer E Posey, Tamar Harel, Pengfei Liu, Jill A Rosenfeld, Regis A James, Zeynep H Coban Akdemir, Magdalena Walkiewicz, Weimin Bi, Rui Xiao, Yan Ding,[...]. N Engl J Med 2017
342
14

Pathogenesis of holoprosencephaly.
Xin Geng, Guillermo Oliver. J Clin Invest 2009
59
14

Cohesin complex-associated holoprosencephaly.
Paul Kruszka, Seth I Berger, Valentina Casa, Mike R Dekker, Jenna Gaesser, Karin Weiss, Ariel F Martinez, David R Murdock, Raymond J Louie, Eloise J Prijoles,[...]. Brain 2019
21
14

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64
14


Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
Mark J McCabe, Carles Gaston-Massuet, Vaitsa Tziaferi, Louise C Gregory, Kyriaki S Alatzoglou, Massimo Signore, Eduardo Puelles, Dianne Gerrelli, I Sadaf Farooqi, Jamal Raza,[...]. J Clin Endocrinol Metab 2011
74
14

Modeling the complex etiology of holoprosencephaly in mice.
Mingi Hong, Robert S Krauss. Am J Med Genet C Semin Med Genet 2018
12
25

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
14


Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
Erich Roessler, Ping Hu, Juliana Marino, Sungkook Hong, Rachel Hart, Seth Berger, Ariel Martinez, Yu Abe, Paul Kruszka, James W Thomas,[...]. Hum Mutat 2018
16
18

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
14

Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.
Xin Geng, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver. Dev Cell 2008
120
14

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
259
14

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Heleen H Arts, Dan Doherty, Sylvia E C van Beersum, Melissa A Parisi, Stef J F Letteboer, Nicholas T Gorden, Theo A Peters, Tina Märker, Krysta Voesenek, Aileen Kartono,[...]. Nat Genet 2007
233
9

Dishevelled stabilization by the ciliopathy protein Rpgrip1l is essential for planar cell polarity.
Alexia Mahuzier, Helori-Mael Gaudé, Valentina Grampa, Isabelle Anselme, Flora Silbermann, Margot Leroux-Berger, Delphine Delacour, Jerome Ezan, Mireille Montcouquiol, Sophie Saunier,[...]. J Cell Biol 2012
43
9


Sonic hedgehog signaling controls thalamic progenitor identity and nuclei specification in mice.
Tou Yia Vue, Krista Bluske, Amin Alishahi, Lin Lin Yang, Naoko Koyano-Nakagawa, Bennett Novitch, Yasushi Nakagawa. J Neurosci 2009
89
9

Spatial and temporal requirements for sonic hedgehog in the regulation of thalamic interneuron identity.
Yongsu Jeong, Diane K Dolson, Ronald R Waclaw, Michael P Matise, Lori Sussel, Kenneth Campbell, Klaus H Kaestner, Douglas J Epstein. Development 2011
53
9


Joubert syndrome: neuroimaging findings in 110 patients in correlation with cognitive function and genetic cause.
Andrea Poretti, Joseph Snow, Angela C Summers, Aylin Tekes, Thierry A G M Huisman, Nafi Aygun, Kathryn A Carson, Dan Doherty, Melissa A Parisi, Camilo Toro,[...]. J Med Genet 2017
31
9

Gene regulatory logic for reading the Sonic Hedgehog signaling gradient in the vertebrate neural tube.
Nikolaos Balaskas, Ana Ribeiro, Jasmina Panovska, Eric Dessaud, Noriaki Sasai, Karen M Page, James Briscoe, Vanessa Ribes. Cell 2012
274
9

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.
Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kàlmàn Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou,[...]. Nat Genet 2007
327
9

The role of Sonic hedgehog of neural origin in thalamic differentiation in the mouse.
Nora-Emöke Szabó, Tianyu Zhao, Xunlei Zhou, Gonzalo Alvarez-Bolado. J Neurosci 2009
57
9

Brain pathology in the Meckel syndrome: a study of 59 cases.
A Paetau, R Salonen, M Haltia. Clin Neuropathol 1985
23
9

Primary cilia control telencephalic patterning and morphogenesis via Gli3 proteolytic processing.
Laurianne Besse, Mariame Neti, Isabelle Anselme, Christoph Gerhardt, Ulrich Rüther, Christine Laclef, Sylvie Schneider-Maunoury. Development 2011
57
9

A highlight on Sonic hedgehog pathway.
Gabriela Basile Carballo, Jéssica Ribeiro Honorato, Giselle Pinto Farias de Lopes, Tania Cristina Leite de Sampaio E Spohr. Cell Commun Signal 2018
115
9

Ftm is a novel basal body protein of cilia involved in Shh signalling.
Jeanette Vierkotten, Renate Dildrop, Thomas Peters, Baolin Wang, Ulrich Rüther. Development 2007
146
9

A crucial role for primary cilia in cortical morphogenesis.
Marc A Willaredt, Kerstin Hasenpusch-Theil, Humphrey A R Gardner, Igor Kitanovic, Vera C Hirschfeld-Warneken, Christian P Gojak, Karin Gorgas, C Lulu Bradford, Joachim Spatz, Stefan Wölfl,[...]. J Neurosci 2008
90
9

Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain.
R W Stottmann, P V Tran, A Turbe-Doan, D R Beier. Dev Biol 2009
55
9

Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis.
Anders Paetau, Heli Honkala, Riitta Salonen, Jaakko Ignatius, Marjo Kestilä, Riitta Herva. J Neuropathol Exp Neurol 2008
12
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.