A citation-based method for searching scientific literature

A C Offiah, M Lees, R M Winter, C M Hall. J Med Genet 2001
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity






SPONASTRIME dysplasia: report on a female patient with severe skeletal changes.
M Masuno, G Nishimura, M Adachi, T Hotsubo, K Tachibana, Y Makita, K Imaizumi, Y Kuroki. Am J Med Genet 1996
12
50

Sponastrime dysplasia. A radiologic-pathologic correlation.
R S Lachman, H Stoss, J Spranger. Pediatr Radiol 1989
28
50

Sponastrime dysplasia: five new cases and review of nine previously published cases.
L O Langer, R K Beals, S LaFranchi, C I Scott, J J Sockalosky. Am J Med Genet 1996
25
50

Sponastrime dysplasia: report on a male patient.
G Camera, A Camera, S Pozzolo, P Costa. Pediatr Radiol 1994
15
33


Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: clinical course and phenotypic variations in four patients.
Gen Nishimura, Tomomi Honma, Takashi Shiihara, Noriyo Manabe, Eiji Nakajima, Masanori Adachi, Makoto Mikawa, Yoshimitsu Fukushima, Shiro Ikegawa. Am J Med Genet A 2003
10
33



RNAi-based screening identifies the Mms22L-Nfkbil2 complex as a novel regulator of DNA replication in human cells.
Wojciech Piwko, Michael H Olma, Michael Held, Julien N Bianco, Patrick G A Pedrioli, Kay Hofmann, Philippe Pasero, Daniel W Gerlich, Matthias Peter. EMBO J 2010
50
33

H4K20me0 marks post-replicative chromatin and recruits the TONSL–MMS22L DNA repair complex.
Giulia Saredi, Hongda Huang, Colin M Hammond, Constance Alabert, Simon Bekker-Jensen, Ignasi Forne, Nazaret Reverón-Gómez, Benjamin M Foster, Lucie Mlejnkova, Till Bartke,[...]. Nature 2016
94
33

The MMS22L-TONSL complex mediates recovery from replication stress and homologous recombination.
Lara O'Donnell, Stephanie Panier, Jan Wildenhain, Johnny M Tkach, Abdallah Al-Hakim, Marie-Claude Landry, Cristina Escribano-Diaz, Rachel K Szilard, Jordan T F Young, Meagan Munro,[...]. Mol Cell 2010
75
33

A genome-wide camptothecin sensitivity screen identifies a mammalian MMS22L-NFKBIL2 complex required for genomic stability.
Brenda C O'Connell, Britt Adamson, John R Lydeard, Mathew E Sowa, Alberto Ciccia, Andrea L Bredemeyer, Michael Schlabach, Steven P Gygi, Stephen J Elledge, J Wade Harper. Mol Cell 2010
71
33

Identification of the MMS22L-TONSL complex that promotes homologous recombination.
Eris Duro, Cecilia Lundin, Katrine Ask, Luis Sanchez-Pulido, Thomas J MacArtney, Rachel Toth, Chris P Ponting, Anja Groth, Thomas Helleday, John Rouse. Mol Cell 2010
64
33

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism.
John J Reynolds, Louise S Bicknell, Paula Carroll, Martin R Higgs, Ranad Shaheen, Jennie E Murray, Dimitrios K Papadopoulos, Andrea Leitch, Olga Murina, Žygimantė Tarnauskaitė,[...]. Nat Genet 2017
45
33

Sponastrime dysplasia with abnormal urinary glycosaminoglycans and growth hormone unresponsiveness.
Vatcharapan Umpaichitra, Robert Wallerstein, Salvador Castells. Clin Dysmorphol 2002
2
100

The MMS22L-TONSL heterodimer directly promotes RAD51-dependent recombination upon replication stress.
Wojciech Piwko, Lucie J Mlejnkova, Karun Mutreja, Lepakshi Ranjha, Diana Stafa, Alexander Smirnov, Mia Ml Brodersen, Ralph Zellweger, Andreas Sturzenegger, Pavel Janscak,[...]. EMBO J 2016
35
33

Another observation of Langer-type sponastrime dysplasia variant.
G Nishimura, M Mikawa, Y Fukushima. Am J Med Genet 1998
10
33


Sponastrime dysplasia: report on two siblings with metal retardation.
G Camera, A Camera, M Di Rocco, R Gatti. Pediatr Radiol 1993
12
16

Heterogeneity of SPONASTRIME dysplasia: delineation of a variant form with severe mental retardation.
A Verloes, J P Misson, J M Dubru, P Jamblin, M Le Merrer. Clin Dysmorphol 1995
7
16

Severe dwarfism with cataracts. A new osteo-chondrodysplasia.
S Chapman, S Bundey, R F Fletcher. Br J Radiol 1990
4
25

A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia.
S F Slaney, C M Hall, D J Atherton, R M Winter. Clin Dysmorphol 1999
19
16


Osteopathia striata, short stature, cataracts, and microdontia: a new syndrome? A case report.
T D Daley, G P Wysocki, R N Bohay. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996
8
16

Short root anomaly.
D M Edwards, G J Roberts. Br Dent J 1990
14
16

Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL).
Athanasios I Tsirikos, Dan E Mason, Charles I Scott, Wei-Ning Chang. Am J Med Genet A 2003
6
16



Nosology and classification of genetic skeletal disorders: 2006 revision.
Andrea Superti-Furga, Sheila Unger. Am J Med Genet A 2007
215
16



The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
16

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
Matthew N Bainbridge, Min Wang, Yuanqing Wu, Irene Newsham, Donna M Muzny, John L Jefferies, Thomas J Albert, Daniel L Burgess, Richard A Gibbs. Genome Biol 2011
145
16

Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia.
Cornelius F Boerkoel, Hiroshi Takashima, Joy John, Jiong Yan, Pawel Stankiewicz, Lisa Rosenbarker, Jean-Luc André, Radovan Bogdanovic, Antoine Burguet, Sandra Cockfield,[...]. Nat Genet 2002
206
16

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
798
16

Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.
Katharina Schlacher, Nicole Christ, Nicolas Siaud, Akinori Egashira, Hong Wu, Maria Jasin. Cell 2011
693
16

Replication dynamics: biases and robustness of DNA fiber analysis.
Hervé Técher, Stéphane Koundrioukoff, Dana Azar, Therese Wilhelm, Sandra Carignon, Olivier Brison, Michelle Debatisse, Benoît Le Tallec. J Mol Biol 2013
68
16

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
603
16

In silico prediction of splice-altering single nucleotide variants in the human genome.
Xueqiu Jian, Eric Boerwinkle, Xiaoming Liu. Nucleic Acids Res 2014
190
16

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
16

Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles.
Denise G Lanza, Angelina Gaspero, Isabel Lorenzo, Lan Liao, Ping Zheng, Ying Wang, Yu Deng, Chonghui Cheng, Chuansheng Zhang, John R Seavitt,[...]. BMC Biol 2018
27
16

MYOD1 involvement in myopathy.
F Lopes, M Miguet, B E Mucha, J Gauthier, V Saillour, C-T É Nguyen, M Vanasse, B Ellezam, J L Michaud, J-F Soucy,[...]. Eur J Neurol 2018
2
50

A two-color acid-free cartilage and bone stain for zebrafish larvae.
M B Walker, C B Kimmel. Biotech Histochem 2007
368
16

Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.
Rivka Sukenik Halevy, Huan-Chieh Chien, Bo Heinz, Michael J Bamshad, Deborah A Nickerson, Martin Kircher, Nadav Ahituv. Hum Mutat 2018
7
16

Efficient gene targeting in zebrafish mediated by a zebrafish-codon-optimized cas9 and evaluation of off-targeting effect.
Da Liu, Zhanxiang Wang, An Xiao, Yutian Zhang, Wenyuan Li, Yao Zu, Shaohua Yao, Shuo Lin, Bo Zhang. J Genet Genomics 2014
51
16

Analysis of the Histone H3.1 Interactome: A Suitable Chaperone for the Right Event.
Eric I Campos, Arne H Smits, Young-Hoon Kang, Sébastien Landry, Thelma M Escobar, Shruti Nayak, Beatrix M Ueberheide, Daniel Durocher, Michiel Vermeulen, Jerard Hurwitz,[...]. Mol Cell 2015
40
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.