A citation-based method for searching scientific literature

G Bradley Schaefer. Int J Mol Sci 2016
Times Cited: 41







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



Times Cited
  Times     Co-cited
Similarity



Advancing the understanding of autism disease mechanisms through genetics.
Luis de la Torre-Ubieta, Hyejung Won, Jason L Stein, Daniel H Geschwind. Nat Med 2016
409
26


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
248
21

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Kristiina Tammimies, Christian R Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C Lionel, Ryan K C Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg,[...]. JAMA 2015
230
19

Parental interest in a genetic risk assessment test for autism spectrum disorders.
Vivien Narcisa, Marie Discenza, Erica Vaccari, Beth Rosen-Sheidley, Antonio Y Hardan, Elizabeth Couchon. Clin Pediatr (Phila) 2013
28
28

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
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,[...]. Am J Hum Genet 2010
19


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
30
23


The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
529
14


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
734
14

In search of biomarkers for autism: scientific, social and ethical challenges.
Pat Walsh, Mayada Elsabbagh, Patrick Bolton, Ilina Singh. Nat Rev Neurosci 2011
140
14

Genetic testing and corresponding services among individuals with autism spectrum disorder (ASD).
Michael L Cuccaro, Kayla Czape, Michael Alessandri, Joycelyn Lee, Abigail Rupchock Deppen, Elise Bendik, Nicole Dueker, Laura Nations, Margaret Pericak-Vance, Susan Hahn. Am J Med Genet A 2014
21
28

Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
49
14


Essential versus complex autism: definition of fundamental prognostic subtypes.
J H Miles, T N Takahashi, S Bagby, P K Sahota, D F Vaslow, C H Wang, R E Hillman, J E Farmer. Am J Med Genet A 2005
142
12

Attitudes and beliefs concerning prostate cancer genetic screening.
David J Doukas, A Russell Localio, Yuelin Li. Clin Genet 2004
24
20

Factors influencing intention to obtain a genetic test for colon cancer risk: a population-based study.
Janice Yanushka Bunn, Kwadwo Bosompra, Takamaru Ashikaga, Brian S Flynn, John K Worden. Prev Med 2002
63
12

Genetic susceptibility testing from a stress and coping perspective.
Holly C Gooding, Kurt Organista, Jeffrey Burack, Barbara Bowles Biesecker. Soc Sci Med 2006
66
12

Autism genetic testing information needs among parents of affected children: A qualitative study.
Ming Li, Ann Amuta, Lei Xu, Shweta U Dhar, Divya Talwar, Eunju Jung, Lei-Shih Chen. Patient Educ Couns 2016
14
35

Parental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.
Fallon R Levine, James E Coxworth, David A Stevenson, Thérèse Tuohy, Randall W Burt, Anita Y Kinney. J Genet Couns 2010
27
18

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
12

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
384
12

Autism genetics: opportunities and challenges for clinical translation.
Jacob A S Vorstman, Jeremy R Parr, Daniel Moreno-De-Luca, Richard J L Anney, John I Nurnberger, Joachim F Hallmayer. Nat Rev Genet 2017
198
12


Autism.
Meng-Chuan Lai, Michael V Lombardo, Simon Baron-Cohen. Lancet 2014
9

The genetics of autism.
Rebecca Muhle, Stephanie V Trentacoste, Isabelle Rapin. Pediatrics 2004
661
9

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
31
12

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
9

Genetics evaluation for the etiologic diagnosis of autism spectrum disorders.
G Bradley Schaefer, Nancy J Mendelsohn. Genet Med 2008
96
9

Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders.
Mari Rossi, Dima El-Khechen, Mary Helen Black, Kelly D Farwell Hagman, Sha Tang, Zöe Powis. Pediatr Neurol 2017
49
9

Identification and evaluation of children with autism spectrum disorders.
Chris Plauché Johnson, Scott M Myers. Pediatrics 2007
934
9


Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
9


The genetic landscape of autism spectrum disorders.
Rasim O Rosti, Abdelrahim A Sadek, Keith K Vaux, Joseph G Gleeson. Dev Med Child Neurol 2014
47
7

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
7

Genetic testing and counseling in the case of an autism diagnosis: A caregivers perspective.
Kristien Hens, Hilde Peeters, Kris Dierickx. Eur J Med Genet 2016
9
33

The genetics of Autism Spectrum Disorders--a guide for clinicians.
Karsten M Heil, Christian P Schaaf. Curr Psychiatry Rep 2013
37
8

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
421
7

Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years--Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012.
Deborah L Christensen, Jon Baio, Kim Van Naarden Braun, Deborah Bilder, Jane Charles, John N Constantino, Julie Daniels, Maureen S Durkin, Robert T Fitzgerald, Margaret Kurzius-Spencer,[...]. MMWR Surveill Summ 2016
853
7

Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
131
7


American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
558
7

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
7

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
818
7

Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality.
Tzyy-Nan Huang, Hsiu-Chun Chuang, Wen-Hsi Chou, Chiung-Ya Chen, Hsiao-Fang Wang, Shen-Ju Chou, Yi-Ping Hsueh. Nat Neurosci 2014
109
7

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
328
7


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.