A citation-based method for searching scientific literature

Erich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge I Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W Belmont, Jeffrey A Towbin, Elizabeth Goldmuntz, Benjamin Feldman, Maximilian Muenke. Am J Hum Genet 2008
Times Cited: 103







List of co-cited articles
1234 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
Bhagyalaxmi Mohapatra, Brett Casey, Hua Li, Trang Ho-Dawson, Liana Smith, Susan D Fernbach, Laura Molinari, Stephen R Niesh, John Lynn Jefferies, William J Craigen,[...]. Hum Mol Genet 2009
95
33

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.
J D Karkera, J S Lee, E Roessler, S Banerjee-Basu, M V Ouspenskaia, J Mez, E Goldmuntz, P Bowers, J Towbin, J W Belmont,[...]. Am J Hum Genet 2007
76
32

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.
Erich Roessler, Wuhong Pei, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge Ivan Veléz, Sharmilla Banerjee-Basu, Gretchen Gibney, Philip J Lupo, Laura E Mitchell, Jeffrey A Towbin,[...]. Mol Genet Metab 2009
51
49

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
301
23

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
80
26

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle.
Elizabeth Goldmuntz, Richard Bamford, Jayaprakash D Karkera, June dela Cruz, Erich Roessler, Maximilian Muenke. Am J Hum Genet 2002
122
20

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.
R N Bamford, E Roessler, R D Burdine, U Saplakoğlu, J dela Cruz, M Splitt, J A Goodship, J Towbin, P Bowers, G B Ferrero,[...]. Nat Genet 2000
233
20

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
20

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
18

Familial transposition of the great arteries caused by multiple mutations in laterality genes.
Alessandro De Luca, Anna Sarkozy, Federica Consoli, Rosangela Ferese, Valentina Guida, Maria Lisa Dentici, Rita Mingarelli, Emanuele Bellacchio, Giulia Tuo, Giuseppe Limongelli,[...]. Heart 2010
82
21

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects.
Stephanie M Ware, Jianlan Peng, Lirong Zhu, Susan Fernbach, Suzanne Colicos, Brett Casey, Jeffrey Towbin, John W Belmont. Am J Hum Genet 2004
173
17

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
159
17

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
17

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
237
17

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
17

Congenital heart disease caused by mutations in the transcription factor NKX2-5.
J J Schott, D W Benson, C T Basson, W Pease, G M Silberbach, J P Moak, B J Maron, C E Seidman, J G Seidman. Science 1998
898
17


X-linked situs abnormalities result from mutations in ZIC3.
M Gebbia, G B Ferrero, G Pilia, M T Bassi, A Aylsworth, M Penman-Splitt, L M Bird, J S Bamforth, J Burn, D Schlessinger,[...]. Nat Genet 1997
305
16


GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
806
16

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
Erich Roessler, Yong Ma, Maia V Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A Beachy, Maximilian Muenke. Hum Genet 2009
50
32

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
283
14

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
115
14

Mutations in NOTCH1 cause aortic valve disease.
Vidu Garg, Alecia N Muth, Joshua F Ransom, Marie K Schluterman, Robert Barnes, Isabelle N King, Paul D Grossfeld, Deepak Srivastava. Nature 2005
925
14

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Edwin P Kirk, Margaret Sunde, Mauro W Costa, Scott A Rankin, Orit Wolstein, M Leticia Castro, Tanya L Butler, Changbaig Hyun, Guanglan Guo, Robyn Otway,[...]. Am J Hum Genet 2007
225
14

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
191
14

Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.
R Kosaki, M Gebbia, K Kosaki, M Lewin, P Bowers, J A Towbin, B Casey. Am J Med Genet 1999
139
13


Disorders of left-right asymmetry: heterotaxy and situs inversus.
Mardi J Sutherland, Stephanie M Ware. Am J Med Genet C Semin Med Genet 2009
143
13

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
12

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects.
Silke Sperling, Christina H Grimm, Ilona Dunkel, Siegrun Mebus, Hans-Peter Sperling, Arno Ebner, Raffaello Galli, Hans Lehrach, Christoph Fusch, Felix Berger,[...]. Hum Mutat 2005
84
14

Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.
Claude Bendavid, Christèle Dubourg, Isabelle Gicquel, Laurent Pasquier, Pascale Saugier-Veber, Marie-Renée Durou, Sylvie Jaillard, Thierry Frébourg, Bassem R Haddad, Catherine Henry,[...]. Hum Genet 2006
43
25

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
11

Functional analysis of mutations in TGIF associated with holoprosencephaly.
Kenia B El-Jaick, Shannon E Powers, Laurent Bartholin, Kenneth R Myers, Jin Hahn, Ieda M Orioli, Maia Ouspenskaia, Felicitas Lacbawan, Erich Roessler, David Wotton,[...]. Mol Genet Metab 2007
55
20

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
11

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
11

Analysis of genotype-phenotype correlations in human holoprosencephaly.
Benjamin D Solomon, Sandra Mercier, Jorge I Vélez, Daniel E Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler,[...]. Am J Med Genet C Semin Med Genet 2010
107
11

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
11

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
297
11

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Mary Ella Pierpont, Craig T Basson, D Woodrow Benson, Bruce D Gelb, Therese M Giglia, Elizabeth Goldmuntz, Glenn McGee, Craig A Sable, Deepak Srivastava, Catherine L Webb. Circulation 2007
532
11

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
C T Basson, D R Bachinsky, R C Lin, T Levi, J A Elkins, J Soults, D Grayzel, E Kroumpouzou, T A Traill, J Leblanc-Straceski,[...]. Nat Genet 1997
773
11

NKX2.5 mutations in patients with tetralogy of fallot.
E Goldmuntz, E Geiger, D W Benson. Circulation 2001
229
11

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Kayoko Hirayama-Yamada, Mitsuhiro Kamisago, Kaoru Akimoto, Hiroyuki Aotsuka, Yoshihide Nakamura, Hideshi Tomita, Michiko Furutani, Shin-ichiro Imamura, Atsuyoshi Takao, Makoto Nakazawa,[...]. Am J Med Genet A 2005
151
10

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.
A Mégarbané, N Salem, E Stephan, R Ashoush, D Lenoir, V Delague, R Kassab, J Loiselet, P Bouvagnet. Eur J Hum Genet 2000
85
11

Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects.
Susan W Robinson, Cynthia D Morris, Elizabeth Goldmuntz, Mark D Reller, Melanie A Jones, Robert D Steiner, Cheryl L Maslen. Am J Hum Genet 2003
118
10

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein.
Yongsu Jeong, Federico Coluccio Leskow, Kenia El-Jaick, Erich Roessler, Maximilian Muenke, Anastasia Yocum, Christele Dubourg, Xue Li, Xin Geng, Guillermo Oliver,[...]. Nat Genet 2008
130
10

Foxh1 is essential for development of the anterior heart field.
Ingo von Both, Cristoforo Silvestri, Tuba Erdemir, Heiko Lickert, Johnathon R Walls, R Mark Henkelman, Janet Rossant, Richard P Harvey, Liliana Attisano, Jeffrey L Wrana. Dev Cell 2004
129
10

A role of the cryptic gene in the correct establishment of the left-right axis.
U Gaio, A Schweickert, A Fischer, A N Garratt, T Müller, C Ozcelik, W Lankes, M Strehle, S Britsch, M Blum,[...]. Curr Biol 1999
101
10


GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.
Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani, Shoichi Arai, Eiji Yamamura, Kunitaka Joo, Takao Takahashi, Rumiko Matsuoka, Hiroyuki Yamagishi. Proc Natl Acad Sci U S A 2009
136
10


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.