A citation-based method for searching scientific literature

N L Lehman, D H Zaleski, W G Sanger, E D Adickes. Am J Med Genet 2001
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals.
Kari A Casas, Tarja K Mononen, Claudia N Mikail, Susan J Hassed, Shibo Li, John J Mulvihill, Henry J Lin, Rena E Falk. Am J Med Genet A 2004
66
44

Clinical phenotype associated with terminal 2q37 deletion.
B Conrad, G Dewald, E Christensen, M Lopez, J Higgins, M E Pierpont. Clin Genet 1995
52
38

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.
M Smith, J R Escamilla, P Filipek, M E Bocian, C Modahl, P Flodman, M A Spence. Cytogenet Cell Genet 2001
41
33

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
33

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome.
G Viot-Szoboszlai, J Amiel, F Doz, M Prieur, J Couturier, J N Zucker, I Henry, A Munnich, M Vekemans, S Lyonnet. Clin Genet 1998
25
33

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.
L C Wilson, K Leverton, M E Oude Luttikhuis, C A Oley, J Flint, J Wolstenholme, D P Duckett, M A Barrow, J V Leonard, A P Read. Am J Hum Genet 1995
121
33


Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype.
E K Bijlsma, C M Aalfs, S Sluitjer, M E Oude Luttikhuis, R C Trembath, J M Hoovers, R C Hennekam. J Med Genet 1999
39
33


Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation.
Paul J Batstone, Sheila Simpson, David T Bonthron, Wee T Keng, Doreen Hamilton, Linda Forsyth, Mark Sales, Norman Pratt, David Goudie. Am J Med Genet A 2003
14
35

Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion.
Daynna J Wolff, Kimberly Clifton, Cynthia Karr, Jane Charles. Genet Med 2002
38
27

Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.
M C Phelan, R C Rogers, K B Clarkson, F P Bowyer, M A Levine, L L Estabrooks, M C Severson, W B Dobyns. Am J Med Genet 1995
84
27


RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.
M M Power, R S James, J C Barber, A M Fisher, P J Wood, B A Leatherdale, D E Flanagan, E Hatchwell. J Med Genet 1997
22
27

Small terminal deletions of the long arm of chromosome 2: two new cases.
A M Fisher, K H Ellis, C E Browne, J C Barber, M Barker, C R Kennedy, H Foley, M A Patton. Am J Med Genet 1994
26
27

Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy.
S P Lin, E M Petty, L H Gibson, J Inserra, M R Seashore, T L Yang-Feng. Am J Med Genet 1992
31
27

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
27

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
27

Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes.
M A Aldred, R O C Sanford, N S Thomas, M A Barrow, L C Wilson, L A Brueton, M C Bonaglia, R C M Hennekam, C Eng, N R Dennis,[...]. J Med Genet 2004
72
27

Deletion (2)(q37).
R F Stratton, J A Tolworthy, R S Young. Am J Med Genet 1994
19
22

Autopsy findings in a severely affected infant with a 2q terminal deletion.
B L Waters, E F Allen, P C Gibson, T Johnston. Am J Med Genet 1993
17
23


Deletion of chromosome 2q37 and autism: a distinct subtype?
M Ghaziuddin, M Burmeister. J Autism Dev Disord 1999
50
22

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
487
22

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
22

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
22

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
22

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
22


Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
137
16

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.
A Weise, H Starke, A Heller, H Tönnies, M Volleth, M Stumm, S Gabriele, A Nietzel, U Claussen, T Liehr. J Med Genet 2002
37
16

STK25 is a candidate gene for pseudopseudohypoparathyroidism.
M S Davids, E Crawford, S Weremowicz, C C Morton, N G Copeland, D J Gilbert, N A Jenkins, M C Phelan, M J Comb, M B Melnick. Genomics 2001
14
21

Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26).
Daniela Giardino, Palma Finelli, Giulietta Gottardi, Gabriella De Canal, Matteo Della Monica, Fortunato Lonardo, Gioacchino Scarano, Lidia Larizza. Am J Med Genet A 2003
18
16


Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.
C D M van Karnebeek, C Koevoets, S Sluijter, E K Bijlsma, D F M C Smeets, E J Redeker, R C M Hennekam, J M N Hoovers. J Med Genet 2002
63
16

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
16

Physical mapping of the holoprosencephaly critical region in 18p11.3.
J Overhauser, H F Mitchell, E H Zackai, D B Tick, K Rojas, M Muenke. Am J Hum Genet 1995
93
16

Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.
N Chassaing, P De Mas, M Tauber, M C Vincent, S Julia, G Bourrouillou, P Calvas, E Bieth. Am J Med Genet A 2004
19
16


Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region.
M Chaabouni, M Le Merrer, O Raoul, M Prieur, M C de Blois, A Philippe, M Vekemans, S P Romana. Eur J Med Genet 2006
24
16

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
C Bendavid, B R Haddad, A Griffin, M Huizing, C Dubourg, I Gicquel, L R Cavalli, L Pasquier, A L Shanske, R Long,[...]. J Med Genet 2006
36
16

GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?
Fedik Rahimov, Lucilene Arilho Ribeiro, Eziquiel de Miranda, Antonio Richieri-Costa, Jeffrey C Murray. Am J Med Genet A 2006
42
16

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
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
16

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
16

Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
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,[...]. Am J Hum Genet 2008
103
16

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.
Deepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, Lakshmi Mehta, Diane W Cox. Genomics 2005
31
16

Chromosome 2q37 deletion: clinical and molecular aspects.
Rena E Falk, Kari A Casas. Am J Med Genet C Semin Med Genet 2007
69
16

Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.
Stephen R Williams, Micheala A Aldred, Vazken M Der Kaloustian, Fahed Halal, Gordon Gowans, D Ross McLeod, Sara Zondag, Helga V Toriello, R Ellen Magenis, Sarah H Elsea. Am J Hum Genet 2010
189
16

Defective forebrain development in mice lacking gp330/megalin.
T E Willnow, J Hilpert, S A Armstrong, A Rohlmann, R E Hammer, D K Burns, J Herz. Proc Natl Acad Sci U S A 1996
397
11


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.