A citation-based method for searching scientific literature

Ron Hochstenbach, Ellen van Binsbergen, John Engelen, Aggie Nieuwint, Abeltje Polstra, Pino Poddighe, Claudia Ruivenkamp, Birgit Sikkema-Raddatz, Dominique Smeets, Martin Poot. Eur J Med Genet 2009
Times Cited: 126







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



Times Cited
  Times     Co-cited
Similarity


Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?
Weimin Bi, Caroline Borgan, Amber N Pursley, Patricia Hixson, Chad A Shaw, Carlos A Bacino, Seema R Lalani, Ankita Patel, Pawel Stankiewicz, James R Lupski,[...]. Genet Med 2013
38
13

Clinical utility of chromosomal microarray analysis.
Jay W Ellison, J Britt Ravnan, Jill A Rosenfeld, S Annie Morton, Nicholas J Neill, Marc S Williams, Jodi Lewis, Beth S Torchia, Cathryn Walker, Ryan N Traylor,[...]. Pediatrics 2012
34
14


Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.
Joanna Wiszniewska, Weimin Bi, Chad Shaw, Pawel Stankiewicz, Sung-Hae L Kang, Amber N Pursley, Seema Lalani, Patricia Hixson, Tomasz Gambin, Chun-hui Tsai,[...]. Eur J Hum Genet 2014
80
6

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
327
5

Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
374
5

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
B W M van Bon, H C Mefford, B Menten, D A Koolen, A J Sharp, W M Nillesen, J W Innis, T J L de Ravel, C L Mercer, M Fichera,[...]. J Med Genet 2009
200
4

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.
J M Friedman, Agnes Baross, Allen D Delaney, Adrian Ally, Laura Arbour, Linlea Armstrong, Jennifer Asano, Dione K Bailey, Sarah Barber, Patricia Birch,[...]. Am J Hum Genet 2006
213
4


European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities.
I Feenstra, J Fang, D A Koolen, A Siezen, C Evans, R M Winter, M M Lees, M Riegel, B B A de Vries, C M A Van Ravenswaaij,[...]. Eur J Med Genet 2006
60
6

Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
Caroline Schluth-Bolard, Bruno Delobel, Damien Sanlaville, Odile Boute, Jean-Marie Cuisset, Sylvie Sukno, Audrey Labalme, Bénédicte Duban-Bedu, Ghislaine Plessis, Sylvie Jaillard,[...]. Eur J Med Genet 2009
77
5

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents.
C Rosenberg, J Knijnenburg, E Bakker, A M Vianna-Morgante, W Sloos, P A Otto, M Kriek, K Hansson, A C V Krepischi-Santos, H Fiegler,[...]. J Med Genet 2006
164
4

Guidelines for molecular karyotyping in constitutional genetic diagnosis.
Joris Robert Vermeesch, Heike Fiegler, Nicole de Leeuw, Karoly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton-Smith, Conny Van Ravenswaaij,[...]. Eur J Hum Genet 2007
103
4

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.
Sang-Jin Park, Eun Hye Jung, Ran-Suk Ryu, Hyun Woong Kang, Jung-Min Ko, Hyon J Kim, Chong Kun Cheon, Sang-Hyun Hwang, Ho-Young Kang. Mol Cytogenet 2011
60
6

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.
Martin Poot, Vera Beyer, Ira Schwaab, Natalja Damatova, Ruben Van't Slot, Jo Prothero, Sue E Holder, Thomas Haaf. Neurogenetics 2010
95
4

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.
Andreas Walter Kuss, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Farkhondeh Behjati, Hossein Darvish, Lia Abbasi-Moheb, Lucia Puettmann, Agnes Zecha, Robert Weissmann,[...]. Hum Genet 2011
38
10

Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Fernanda Sarquis Jehee, Jean Tetsuo Takamori, Paula F Vasconcelos Medeiros, Ana Carolina B Pordeus, Flavia Roche M Latini, Débora Romeo Bertola, Chong Ae Kim, Maria Rita Passos-Bueno. Eur J Med Genet 2011
31
12

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
David A Koolen, Lisenka E L M Vissers, Rolph Pfundt, Nicole de Leeuw, Samantha J L Knight, Regina Regan, R Frank Kooy, Edwin Reyniers, Corrado Romano, Marco Fichera,[...]. Nat Genet 2006
299
4

Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.
Nicholas J Neill, Blake C Ballif, Allen N Lamb, Sumit Parikh, J Britt Ravnan, Roger A Schultz, Beth S Torchia, Jill A Rosenfeld, Lisa G Shaffer. Genome Res 2011
35
11

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Anna C Need, Nicole M Walley, Paola Nicoletti, Dongliang Ge, Claudia B Catarino,[...]. Am J Hum Genet 2010
176
4

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?
Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, Ian B Gibson, Zhilian Xia, Sangeetha Mahadevan, Joanna Wiszniewska, Carlos A Bacino, Seema Lalani, Lorraine Potocki,[...]. Hum Mutat 2010
97
4

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak,[...]. Nat Genet 2009
396
4

Identification of incestuous parental relationships by SNP-based DNA microarrays.
C P Schaaf, D A Scott, J Wiszniewska, A L Beaudet. Lancet 2011
41
9

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
122
4

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
139
4


Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, Lisa G Shaffer. Prenat Diagn 2011
39
10

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
Bassem A Bejjani, Reza Saleki, Blake C Ballif, Emily A Rorem, Kyle Sundin, Aaron Theisen, Catherine D Kashork, Lisa G Shaffer. Am J Med Genet A 2005
160
4

Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics.
Nicolien M Hanemaaijer, Birgit Sikkema-Raddatz, Gerben van der Vries, Trijnie Dijkhuizen, Roel Hordijk, Anthonie J van Essen, Hermine E Veenstra-Knol, Wilhelmina S Kerstjens-Frederikse, Johanna C Herkert, Erica H Gerkes,[...]. Eur J Hum Genet 2012
48
8

Fragile X and X-linked intellectual disability: four decades of discovery.
Herbert A Lubs, Roger E Stevenson, Charles E Schwartz. Am J Hum Genet 2012
135
4

Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects.
Marjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, Bregje W M van Bon, Thessa Kroes, Joep de Ligt, Bert B de Vries, Jeroen Schoots, Dorien Lugtenberg, Ben C J Hamel,[...]. J Med Genet 2012
102
4

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
Blake C Ballif, Jill A Rosenfeld, Ryan Traylor, Aaron Theisen, Patricia I Bader, Roger L Ladda, Susan L Sell, Michelle Steinraths, Urvashi Surti, Marianne McGuire,[...]. Hum Genet 2012
83
4

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.
Michael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, Bregje W M van Bon, Yiping Shen, Elena A Repnikova, Julie Gastier-Foster, Devon Lamb Thrush, Sekar Kathiresan, Douglas M Ruderfer,[...]. Am J Hum Genet 2011
140
4

Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay.
Margaret P Adam, April N Justice, Susan Schelley, Andrea Kwan, Louanne Hudgins, Christa L Martin. J Pediatr 2009
22
18

Mechanisms for recurrent and complex human genomic rearrangements.
Pengfei Liu, Claudia M B Carvalho, P J Hastings, James R Lupski. Curr Opin Genet Dev 2012
214
4

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
136
4

Copy number variants, diseases and gene expression.
Charlotte N Henrichsen, Evelyne Chaignat, Alexandre Reymond. Hum Mol Genet 2009
272
4

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.
Jan P Schouten, Cathal J McElgunn, Raymond Waaijer, Danny Zwijnenburg, Filip Diepvens, Gerard Pals. Nucleic Acids Res 2002
4

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
61
6

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino,[...]. PLoS One 2007
164
4

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
208
4

De novo rates and selection of large copy number variation.
Andy Itsara, Hao Wu, Joshua D Smith, Deborah A Nickerson, Isabelle Romieu, Stephanie J London, Evan E Eichler. Genome Res 2010
195
4

CNVs of noncoding cis-regulatory elements in human disease.
Malte Spielmann, Eva Klopocki. Curr Opin Genet Dev 2013
31
12

Prevalence of intellectual disability: a meta-analysis of population-based studies.
Pallab K Maulik, Maya N Mascarenhas, Colin D Mathers, Tarun Dua, Shekhar Saxena. Res Dev Disabil 2011
575
4

Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
D A Koolen, W M Nillesen, M H A Versteeg, G F M Merkx, N V A M Knoers, M Kets, S Vermeer, C M A van Ravenswaaij, C G de Kovel, H G Brunner,[...]. J Med Genet 2004
119
4

Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patients.
Linda Siggberg, Sirpa Ala-Mello, Elisa Jaakkola, Esa Kuusinen, Robert Schuit, Jürgen Kohlhase, Detlef Böhm, Jaakko Ignatius, Sakari Knuutila. Am J Med Genet A 2010
29
13

Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.
Caroline Schluth-Bolard, Audrey Labalme, Marie-Pierre Cordier, Marianne Till, Gwenaël Nadeau, Hélène Tevissen, Gaétan Lesca, Nadia Boutry-Kryza, Sylvie Rossignol, Delphine Rocas,[...]. J Med Genet 2013
67
5


Exome sequencing identifies the cause of a mendelian disorder.
Sarah B Ng, Kati J Buckingham, Choli Lee, Abigail W Bigham, Holly K Tabor, Karin M Dent, Chad D Huff, Paul T Shannon, Ethylin Wang Jabs, Deborah A Nickerson,[...]. Nat Genet 2010
4

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
4


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.