A citation-based method for searching scientific literature

David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1469







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



Times Cited
  Times     Co-cited
Similarity


[Editorial: Medical ethics in medical care services].
P Kassab. AMB Rev Assoc Med Bras 1973
63
3



Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction.
Xie Yingjun, Hu Zhiyang, Lin Linhua, Su Fangming, Huang Linhuan, Tan Jinfeng, Pang Qianying, Sun Xiaofang. Eur J Obstet Gynecol Reprod Biol 2017
9
22

Extended tracts of homozygosity in outbred human populations.
Jane Gibson, Newton E Morton, Andrew Collins. Hum Mol Genet 2006
221
2

Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.
Brynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, Melissa K Maisenbacher, Megan P Hall, Zachary Demko, Ruth B Lathi, Rosina Tao, Vimla Aggarwal, Matthew Rabinowitz. Obstet Gynecol 2014
88
2

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States.
Ginger J Tsai, Carrie A Cameron, Jennifer L Czerwinski, Hector Mendez-Figueroa, Susan K Peterson, Sarah Jane Noblin. J Genet Couns 2017
9
22

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, E Robert Wassman, Adrianne L Baxter, Charles H Hensel, Megan M Martin, Aparna Prasad, Hope Twede, Rena J Vanzo, Merlin G Butler. Int J Mol Sci 2016
25
8


Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Elliott Rees, Kimberley Kendall, Antonio F Pardiñas, Sophie E Legge, Andrew Pocklington, Valentina Escott-Price, James H MacCabe, David A Collier, Peter Holmans, Michael C O'Donovan,[...]. JAMA Psychiatry 2016
53
3

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
71
2

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
189
2

Exome sequence read depth methods for identifying copy number changes.
Latha Kadalayil, Sajjad Rafiq, Matthew J J Rose-Zerilli, Reuben J Pengelly, Helen Parker, David Oscier, Jonathan C Strefford, William J Tapper, Jane Gibson, Sarah Ennis,[...]. Brief Bioinform 2015
46
4

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls.
Justin M Zook, Brad Chapman, Jason Wang, David Mittelman, Oliver Hofmann, Winston Hide, Marc Salit. Nat Biotechnol 2014
410
2

A robust model for read count data in exome sequencing experiments and implications for copy number variant calling.
Vincent Plagnol, James Curtis, Michael Epstein, Kin Y Mok, Emma Stebbings, Sofia Grigoriadou, Nicholas W Wood, Sophie Hambleton, Siobhan O Burns, Adrian J Thrasher,[...]. Bioinformatics 2012
288
2

AUDIOME: a tiered exome sequencing-based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss.
Qiaoning Guan, Jorune Balciuniene, Kajia Cao, Zhiqian Fan, Sawona Biswas, Alisha Wilkens, Daniel J Gallo, Emma Bedoukian, Jennifer Tarpinian, Pushkala Jayaraman,[...]. Genet Med 2018
10
20


Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
70
2

CNV biology in neurodevelopmental disorders.
Toru Takumi, Kota Tamada. Curr Opin Neurobiol 2018
36
5

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
2

Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.
Eleonora Napoli, Serena Russo, Laura Casula, Viola Alesi, Filomena Alessandra Amendola, Adriano Angioni, Antonio Novelli, Giovanni Valeri, Deny Menghini, Stefano Vicari. J Autism Dev Disord 2018
10
20

Diagnostic implications of genetic copy number variation in epilepsy plus.
Antonietta Coppola, Elena Cellini, Hannah Stamberger, Elmo Saarentaus, Valentina Cetica, Dennis Lal, Tania Djémié, Magdalena Bartnik-Glaska, Berten Ceulemans, J Helen Cross,[...]. Epilepsia 2019
26
7



Genetic heritability and shared environmental factors among twin pairs with autism.
Joachim Hallmayer, Sue Cleveland, Andrea Torres, Jennifer Phillips, Brianne Cohen, Tiffany Torigoe, Janet Miller, Angie Fedele, Jack Collins, Karen Smith,[...]. Arch Gen Psychiatry 2011
962
2

Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders.
Hjördis O Atladóttir, Poul Thorsen, Lars Østergaard, Diana E Schendel, Sanne Lemcke, Morsi Abdallah, Erik T Parner. J Autism Dev Disord 2010
462
2

Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders.
Elaine Y Hsiao, Sara W McBride, Sophia Hsien, Gil Sharon, Embriette R Hyde, Tyler McCue, Julian A Codelli, Janet Chow, Sarah E Reisman, Joseph F Petrosino,[...]. Cell 2013
2

Prevalence of autism spectrum disorder phenomenology in genetic disorders: a systematic review and meta-analysis.
Caroline Richards, Christopher Jones, Laura Groves, Jo Moss, Chris Oliver. Lancet Psychiatry 2015
136
2

The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
476
2

Autism after infection, febrile episodes, and antibiotic use during pregnancy: an exploratory study.
Hjördis Ósk Atladóttir, Tine Brink Henriksen, Diana E Schendel, Erik T Parner. Pediatrics 2012
198
2


Genetics and epigenetics of autism spectrum disorder-current evidence in the field.
Barbara Wiśniowiecka-Kowalnik, Beata Anna Nowakowska. J Appl Genet 2019
41
4

The epidemiology and global burden of autism spectrum disorders.
A J Baxter, T S Brugha, H E Erskine, R W Scheurer, T Vos, J G Scott. Psychol Med 2015
329
2

Characteristics and concordance of autism spectrum disorders among 277 twin pairs.
Rebecca E Rosenberg, J Kiely Law, Gayane Yenokyan, John McGready, Walter E Kaufmann, Paul A Law. Arch Pediatr Adolesc Med 2009
205
2

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample.
Emma Colvert, Beata Tick, Fiona McEwen, Catherine Stewart, Sarah R Curran, Emma Woodhouse, Nicola Gillan, Victoria Hallett, Stephanie Lietz, Tracy Garnett,[...]. JAMA Psychiatry 2015
192
2

Prevalence of autism spectrum disorders in a total population sample.
Young Shin Kim, Bennett L Leventhal, Yun-Joo Koh, Eric Fombonne, Eugene Laska, Eun-Chung Lim, Keun-Ah Cheon, Soo-Jeong Kim, Young-Key Kim, Hyunkyung Lee,[...]. Am J Psychiatry 2011
621
2

Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP).
Gillian Baird, Emily Simonoff, Andrew Pickles, Susie Chandler, Tom Loucas, David Meldrum, Tony Charman. Lancet 2006
981
2

Genomics, intellectual disability, and autism.
Heather C Mefford, Mark L Batshaw, Eric P Hoffman. N Engl J Med 2012
177
2

Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study.
Sally Ozonoff, Gregory S Young, Alice Carter, Daniel Messinger, Nurit Yirmiya, Lonnie Zwaigenbaum, Susan Bryson, Leslie J Carver, John N Constantino, Karen Dobkins,[...]. Pediatrics 2011
661
2

The Prevalence of Parent-Reported Autism Spectrum Disorder Among US Children.
Michael D Kogan, Catherine J Vladutiu, Laura A Schieve, Reem M Ghandour, Stephen J Blumberg, Benjamin Zablotsky, James M Perrin, Paul Shattuck, Karen A Kuhlthau, Robin L Harwood,[...]. Pediatrics 2018
100
2

Rate of de novo mutations and the importance of father's age to disease risk.
Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir,[...]. Nature 2012
2


Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
287
2

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
D B McElhinney, B J Clark, P M Weinberg, M L Kenton, D McDonald-McGinn, D A Driscoll, E H Zackai, E Goldmuntz. J Am Coll Cardiol 2001
148
2

Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
113
2

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
404
2

Aberrant right subclavian artery (ARSA) in unselected population at first and second trimester ultrasonography.
G Rembouskos, U Passamonti, V De Robertis, A Tempesta, G Campobasso, G Volpe, M Gentile, P Volpe. Prenat Diagn 2012
29
6

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
919
2

A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Aparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, John Wei, Anath C Lionel, Daisuke Sato, Jessica Rickaby, Chao Lu, Peter Szatmari, Wendy Roberts,[...]. G3 (Bethesda) 2012
122
2

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
78
2


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.