A citation-based method for searching scientific literature

Hussam Al-Kateb, Geetika Khanna, Isabel Filges, Natalie Hauser, Dorothy K Grange, Joseph Shen, Christopher D Smyser, Shashikant Kulkarni, Marwan Shinawi. Am J Med Genet A 2014
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, H Xie,[...]. N Engl J Med 2015
145
54

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
317
50

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
41

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D Beckmann,[...]. Nature 2011
264
37

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
37

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens,[...]. Nature 2010
317
37

Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.
Duncan B Sparrow, Aideen McInerney-Leo, Zoran S Gucev, Brooke Gardiner, Mhairi Marshall, Paul J Leo, Deborah L Chapman, Velibor Tasic, Abduhadi Shishko, Matthew A Brown,[...]. Hum Mol Genet 2013
56
37

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.
Keiko Shimojima, Takehiko Inoue, Yuji Fujii, Kousaku Ohno, Toshiyuki Yamamoto. Eur J Med Genet 2009
32
33

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Bridget A Fernandez, Wendy Roberts, Brian Chung, Rosanna Weksberg, Stephen Meyn, Peter Szatmari, Ann M Joseph-George, Sara Mackay, Kathy Whitten, Barbara Noble,[...]. J Med Genet 2010
163
25

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.
Yiping Shen, Xiaoli Chen, Liwen Wang, Jin Guo, Jianliang Shen, Yu An, Haitao Zhu, Yanli Zhu, Ruolei Xin, Yihua Bao,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
22
27

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications.
Jill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, Santhosh Girirajan, Evan E Eichler, Lisa G Shaffer, Blake C Ballif. J Neurodev Disord 2010
106
25

A mechanism for gene-environment interaction in the etiology of congenital scoliosis.
Duncan B Sparrow, Gavin Chapman, Allanceson J Smith, Muhammad Z Mattar, Joelene A Major, Victoria C O'Reilly, Yumiko Saga, Elaine H Zackai, John P Dormans, Benjamin A Alman,[...]. Cell 2012
125
25


The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
25

Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis.
M Lefebvre, Y Duffourd, T Jouan, C Poe, N Jean-Marçais, A Verloes, J St-Onge, J-B Riviere, F Petit, G Pierquin,[...]. Clin Genet 2017
19
31

Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia.
Christian P Schaaf, Robin P Goin-Kochel, Kerri P Nowell, Jill V Hunter, Kirk A Aleck, Sarah Cox, Ankita Patel, Carlos A Bacino, Marwan Shinawi. Eur J Hum Genet 2011
34
20

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
20

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
251
20

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
E K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, A van Haeringen, D E Fransen van de Putte, B-M Anderlid, J Lundin, P Lapunzina, L A Pérez Jurado, B Delle Chiaie,[...]. Eur J Med Genet 2009
168
20

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
478
20

Opposing brain differences in 16p11.2 deletion and duplication carriers.
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
90
20

Tbx6, a mouse T-Box gene implicated in paraxial mesoderm formation at gastrulation.
D L Chapman, I Agulnik, S Hancock, L M Silver, V E Papaioannou. Dev Biol 1996
214
20

Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis.
Kazuki Takeda, Ikuyo Kou, Noriaki Kawakami, Aritoshi Iida, Masahiro Nakajima, Yoji Ogura, Eri Imagawa, Noriko Miyake, Naomichi Matsumoto, Yukuto Yasuhiko,[...]. Hum Mutat 2017
25
20

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
16

The mouse rib-vertebrae mutation is a hypomorphic Tbx6 allele.
Masami Watabe-Rudolph, Nicole Schlautmann, Virginia E Papaioannou, Achim Gossler. Mech Dev 2002
56
16

A missense T (Brachyury) mutation contributes to vertebral malformations.
Nader Ghebranious, Robert D Blank, Cathleen L Raggio, Justin Staubli, Elizabeth McPherson, Lynn Ivacic, Kristen Rasmussen, F Stig Jacobsen, Thomas Faciszewski, James K Burmester,[...]. J Bone Miner Res 2008
39
16

Defective somite patterning in mouse embryos with reduced levels of Tbx6.
Phillip H White, Deborah R Farkas, Erin E McFadden, Deborah L Chapman. Development 2003
79
16

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
16

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
16

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A M Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, S Adaszewski, J Dukart, C Ferrari, P Conus, K Männik,[...]. Mol Psychiatry 2015
93
16

Clinical, genetic and environmental factors associated with congenital vertebral malformations.
P F Giampietro, C L Raggio, R D Blank, C McCarty, U Broeckel, M A Pickart. Mol Syndromol 2013
44
16

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.
C Hernando, A Plaja, M A Rigola, M M Pérez, T Vendrell, J Egocue, C Fuster. J Med Genet 2002
31
12

A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
Yohei Takahashi, Ikuyo Kou, Atsushi Takahashi, Todd A Johnson, Katsuki Kono, Noriaki Kawakami, Koki Uno, Manabu Ito, Shohei Minami, Haruhisa Yanagida,[...]. Nat Genet 2011
143
12

Identification of candidate regions for familial idiopathic scoliosis.
Nancy H Miller, Cristina M Justice, Beth Marosy, Kimberly F Doheny, Elizabeth Pugh, Jun Zhang, Harry C Dietz, Alexander F Wilson. Spine (Phila Pa 1976) 2005
98
12

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis.
Ikuyo Kou, Yohei Takahashi, Todd A Johnson, Atsushi Takahashi, Long Guo, Jin Dai, Xusheng Qiu, Swarkar Sharma, Aki Takimoto, Yoji Ogura,[...]. Nat Genet 2013
140
12

Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2.
Nancy H Miller, Cristina M Justice, Beth Marosy, Kandice Swindle, Yoonhee Kim, Marie-Hélène Roy-Gagnon, Heejong Sung, Dana Behneman, Kimberly F Doheny, Elizabeth Pugh,[...]. Hum Hered 2012
10
30

Structural variation in the human genome and its role in disease.
Paweł Stankiewicz, James R Lupski. Annu Rev Med 2010
670
12

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.
Swarkar Sharma, Xiaochong Gao, Douglas Londono, Shonn E Devroy, Kristen N Mauldin, Jessica T Frankel, January M Brandon, Dongping Zhang, Quan-Zhen Li, Matthew B Dobbs,[...]. Hum Mol Genet 2011
116
12

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
643
12


An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
12


The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.
Qi Fei, Zhihong Wu, Hai Wang, Xi Zhou, Naiguo Wang, Yaozhong Ding, Yipeng Wang, Guixing Qiu. Spine (Phila Pa 1976) 2010
23
13

Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans.
Philip F Giampietro, Sally L Dunwoodie, Kenro Kusumi, Olivier Pourquié, Olivier Tassy, Amaka C Offiah, Alberto S Cornier, Benjamin A Alman, Robert D Blank, Cathleen L Raggio,[...]. Ann N Y Acad Sci 2009
39
12

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
12

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
12

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
12

Aberrant white matter microstructure in children with 16p11.2 deletions.
Julia P Owen, Yi Shin Chang, Nicholas J Pojman, Polina Bukshpun, Mari L J Wakahiro, Elysa J Marco, Jeffrey I Berman, John E Spiro, Wendy K Chung, Randy L Buckner,[...]. J Neurosci 2014
49
12

Segmental border is defined by Ripply2-mediated Tbx6 repression independent of Mesp2.
Wei Zhao, Rieko Ajima, Youichirou Ninomiya, Yumiko Saga. Dev Biol 2015
15
20

Pilot assessment of a radiologic classification system for segmentation defects of the vertebrae.
Amaka Offiah, Benjamin Alman, Alberto S Cornier, Philip F Giampietro, Olivier Tassy, Angie Wade, Peter D Turnpenny. Am J Med Genet A 2010
29
12


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.