A citation-based method for searching scientific literature

Darrel Waggoner, Karen E Wain, Adrian M Dubuc, Laura Conlin, Scott E Hickey, Allen N Lamb, Christa Lese Martin, Cynthia C Morton, Kristen Rasmussen, Jane L Schuette, Stuart Schwartz, David T Miller. Genet Med 2018
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


Underutilization of genetics services for autism: the importance of parental awareness and provider recommendation.
Kimberly Vande Wydeven, Andrea Kwan, Antonio Y Hardan, Jonathan A Bernstein. J Genet Couns 2012
29
9

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
44
9

Needs assessment in genetic testing education: A survey of parents of children with autism spectrum disorder in the united states.
Shixi Zhao, Wei-Ju Chen, Shweta U Dhar, Tanya N Eble, Oi-Man Kwok, Lei-Shih Chen. Autism Res 2019
6
33

Provision of Genetic Services for Autism and its Impact on Spanish Families.
Marta Codina-Solà, Luis A Pérez-Jurado, Ivon Cuscó, Clara Serra-Juhé. J Autism Dev Disord 2017
6
33

Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017
53
9

Whole-genome sequencing of quartet families with autism spectrum disorder.
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
297
9

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Robert W Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne S Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow,[...]. Nat Med 2020
20
10

Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample.
Daniel Moreno-De-Luca, Brian C Kavanaugh, Carrie R Best, Stephen J Sheinkopf, Chanika Phornphutkul, Eric M Morrow. JAMA Psychiatry 2020
6
33

Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society.
P A Filipek, P J Accardo, S Ashwal, G T Baranek, E H Cook, G Dawson, B Gordon, J S Gravel, C P Johnson, R J Kallen,[...]. Neurology 2000
477
9

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
357
9

Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.
Saul A Mullen, Gemma L Carvill, Susannah Bellows, Marta A Bayly, Holger Trucks, Dennis Lal, Thoman Sander, Samuel F Berkovic, Leanne M Dibbens, Ingrid E Scheffer,[...]. Neurology 2013
95
9

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.
Yanjie Fan, Yanming Wu, Lili Wang, Yu Wang, Zhuwen Gong, Wenjuan Qiu, Jingmin Wang, Huiwen Zhang, Xing Ji, Jun Ye,[...]. BMC Med Genomics 2018
11
18

Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability.
Francesca M Snoeijen-Schouwenaars, Jans S van Ool, Judith S Verhoeven, Petra van Mierlo, Hilde M H Braakman, Eric E Smeets, Joost Nicolai, Jeroen Schoots, Mariel W A Teunissen, Rob P W Rouhl,[...]. Epilepsia 2019
29
9

Clinical and genetic spectrum of a large cohort of children with epilepsy in China.
Lin Yang, Yanting Kong, Xinran Dong, Liyuan Hu, Yifeng Lin, Xiang Chen, Qi Ni, Yulan Lu, Bingbing Wu, Huijun Wang,[...]. Genet Med 2019
40
9

Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG).
Daniela Del Gaudio, Marwan Shinawi, Caroline Astbury, Marwan K Tayeh, Kristen L Deak, Gordana Raca. Genet Med 2020
22
9

Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.
Xinran Dong, Bo Liu, Lin Yang, Huijun Wang, Bingbing Wu, Renchao Liu, Hongbo Chen, Xiang Chen, Sha Yu, Bin Chen,[...]. J Med Genet 2020
15
13

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
Diana W Bianchi, Lawrence D Platt, James D Goldberg, Alfred Z Abuhamad, Amy J Sehnert, Richard P Rava. Obstet Gynecol 2012
455
9

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
200
9

Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders.
Oliver James Dillon, Sebastian Lunke, Zornitza Stark, Alison Yeung, Natalie Thorne, Clara Gaff, Susan M White, Tiong Yang Tan. Eur J Hum Genet 2018
50
9

The genetics of microdeletion and microduplication syndromes: an update.
Corey T Watson, Tomas Marques-Bonet, Andrew J Sharp, Heather C Mefford. Annu Rev Genomics Hum Genet 2014
82
9

Genetic disorders and mortality in infancy and early childhood: delayed diagnoses and missed opportunities.
Monica H Wojcik, Talia S Schwartz, Inbar Yamin, Heather L Edward, Casie A Genetti, Meghan C Towne, Pankaj B Agrawal. Genet Med 2018
22
9

De novo mutations in regulatory elements in neurodevelopmental disorders.
Patrick J Short, Jeremy F McRae, Giuseppe Gallone, Alejandro Sifrim, Hyejung Won, Daniel H Geschwind, Caroline F Wright, Helen V Firth, David R FitzPatrick, Jeffrey C Barrett,[...]. Nature 2018
98
9

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Josh E Petrikin, Julie A Cakici, Michelle M Clark, Laurel K Willig, Nathaly M Sweeney, Emily G Farrow, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Lee Zellmer,[...]. NPJ Genom Med 2018
82
9

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F Kingsmore, Julie A Cakici, Michelle M Clark, Mary Gaughran, Michele Feddock, Sergey Batalov, Matthew N Bainbridge, Jeanne Carroll, Sara A Caylor, Christina Clarke,[...]. Am J Hum Genet 2019
73
9

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
9

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam,[...]. Genet Med 2018
188
9

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
163
9

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children.
Courtney E French, Isabelle Delon, Helen Dolling, Alba Sanchis-Juan, Olga Shamardina, Karyn Mégy, Stephen Abbs, Topun Austin, Sarah Bowdin, Ricardo G Branco,[...]. Intensive Care Med 2019
63
9

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant,[...]. Nat Genet 2017
289
9

Rapid Targeted Genomics in Critically Ill Newborns.
Cleo C van Diemen, Wilhelmina S Kerstjens-Frederikse, Klasien A Bergman, Tom J de Koning, Birgit Sikkema-Raddatz, Joeri K van der Velde, Kristin M Abbott, Johanna C Herkert, Katharina Löhner, Patrick Rump,[...]. Pediatrics 2017
51
9

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist,[...]. Lancet Respir Med 2015
182
9


Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder?
Sureni V Mullegama, Steven D Klein, Dzung C Nguyen, Arang Kim, Rebecca Signer, Michelle Fox, Naghmeh Dorrani, Andrea Hendershot, Rebecca Mardach, Robert Suddath,[...]. Genet Med 2017
10
20


Fragile X testing as a second-tier test.
Taila Hartley, Ryan Potter, Lauren Badalato, Amanda C Smith, Olga Jarinova, Kym M Boycott. Genet Med 2017
5
40

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, Hope Twede, Rena Vanzo, Erin Harward, Charles H Hensel, Megan M Martin, Stephanie Page, Andreas Peiffer, Patricia Mowery-Rushton, Moises Serrano,[...]. Biomed Res Int 2016
12
16

Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
243
9

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
9



Re-evaluating the first-tier status of fragile X testing in neurodevelopmental disorders.
Lauren A Borch, Jillian Parboosingh, Mary Ann Thomas, Pamela Veale. Genet Med 2020
8
25

Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability.
Jin Sook Lee, Hee Hwang, Soo Yeon Kim, Ki Joong Kim, Jin Sun Choi, Mi Jung Woo, Young Min Choi, Jong Kwan Jun, Byung Chan Lim, Jong Hee Chae. Ann Lab Med 2018
15
6

Phenotype in patients with intellectual disability and pathological results in array CGH.
V Caballero Pérez, F J López Pisón, M D Miramar Gallart, A González Álvarez, M C García Jiménez, J P García Iñiguez, C Orden Rueda, I Gil Hernández, C Fuertes Rodrigo, R Fernando Martínez,[...]. Neurologia 2017
4
25

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
Lisenka E L M Vissers, Bert B A de Vries, Kazutoyo Osoegawa, Irene M Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik H L P G Huys, Anke van Rijk,[...]. Am J Hum Genet 2003
344
4

Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.
Emma Palmer, Helen Speirs, Peter J Taylor, Glenda Mullan, Gill Turner, Stewart Einfeld, Bruce Tonge, David Mowat. Am J Med Genet A 2014
31
4

Interpretation of array comparative genome hybridization data: a major challenge.
A C J Gijsbers, J Schoumans, C A L Ruivenkamp. Cytogenet Genome Res 2011
25
4

Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
G S Vianna, P F V Medeiros, A F Alves, T O Silva, F S Jehee. Genet Mol Res 2016
7
14

Pathogenic or not? Assessing the clinical relevance of copy number variants.
J Y Hehir-Kwa, R Pfundt, J A Veltman, N de Leeuw. Clin Genet 2013
36
4

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies.
Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C Rivera, María L Guzmán, Gabriela M Repetto. J Pediatr (Rio J) 2015
6
16

A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature.
Elaine Lustosa-Mendes, Ana Paula Dos Santos, Nilma Lúcia Viguetti-Campos, Társis Paiva Vieira, Vera Lúcia Gil-da-Silva-Lopes. Am J Med Genet A 2017
7
14


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.