A citation-based method for searching scientific literature

Barbara Bowles Biesecker, Holly Landrum Peay. Int J Neuropsychopharmacol 2013
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
33

Attitudes to genetic testing in families with multiple cases of bipolar disorder.
Bettina Meiser, Nadine A Kasparian, Philip B Mitchell, Kimberly Strong, Judy M Simpson, Laila Tabassum, Shab Mireskandari, Peter R Schofield. Genet Test 2008
37
33

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011
474
25

A standard variation file format for human genome sequences.
Martin G Reese, Barry Moore, Colin Batchelor, Fidel Salas, Fiona Cunningham, Gabor T Marth, Lincoln Stein, Paul Flicek, Mark Yandell, Karen Eilbeck. Genome Biol 2010
61
25

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing.
Jason O'Rawe, Tao Jiang, Guangqing Sun, Yiyang Wu, Wei Wang, Jingchu Hu, Paul Bodily, Lifeng Tian, Hakon Hakonarson, W Evan Johnson,[...]. Genome Med 2013
276
25

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
25

Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.
Iris Schrijver, Nazneen Aziz, Daniel H Farkas, Manohar Furtado, Andrea Ferreira Gonzalez, Timothy C Greiner, Wayne W Grody, Tina Hambuch, Lisa Kalman, Jeffrey A Kant,[...]. J Mol Diagn 2012
104
25

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
760
25

Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet Med 2012
122
25


Pilot study on patients' and spouses' attitudes toward potential genetic testing for bipolar disorder.
C L Trippitelli, K R Jamison, M F Folstein, J J Bartko, J R DePaulo. Am J Psychiatry 1998
68
25

Implications of genetic risk information in families with a high density of bipolar disorder: an exploratory study.
Bettina Meiser, Philip B Mitchell, H McGirr, M Van Herten, Peter R Schofield. Soc Sci Med 2005
67
25


Consensus generation and variant detection by Celera Assembler.
Gennady Denisov, Brian Walenz, Aaron L Halpern, Jason Miller, Nelson Axelrod, Samuel Levy, Granger Sutton. Bioinformatics 2008
54
16

Non-redundant compendium of human ncRNA genes in GeneCards.
Frida Belinky, Iris Bahir, Gil Stelzer, Shahar Zimmerman, Naomi Rosen, Noam Nativ, Irina Dalah, Tsippi Iny Stein, Noa Rappaport, Toutai Mituyama,[...]. Bioinformatics 2013
31
16

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.
Hui Shen, Jian Li, Jigang Zhang, Chao Xu, Yan Jiang, Zikai Wu, Fuping Zhao, Li Liao, Jun Chen, Yong Lin,[...]. PLoS One 2013
37
16


Genomics in clinical practice: lessons from the front lines.
Howard J Jacob, Kelly Abrams, David P Bick, Kent Brodie, David P Dimmock, Michael Farrell, Jennifer Geurts, Jeremy Harris, Daniel Helbling, Barbara J Joers,[...]. Sci Transl Med 2013
67
16


Pacific biosciences sequencing technology for genotyping and variation discovery in human data.
Mauricio O Carneiro, Carsten Russ, Michael G Ross, Stacey B Gabriel, Chad Nusbaum, Mark A DePristo. BMC Genomics 2012
132
16

Modernizing reference genome assemblies.
Deanna M Church, Valerie A Schneider, Tina Graves, Katherine Auger, Fiona Cunningham, Nathan Bouk, Hsiu-Chuan Chen, Richa Agarwala, William M McLaren, Graham R S Ritchie,[...]. PLoS Biol 2011
207
16

VarScan: variant detection in massively parallel sequencing of individual and pooled samples.
Daniel C Koboldt, Ken Chen, Todd Wylie, David E Larson, Michael D McLellan, Elaine R Mardis, George M Weinstock, Richard K Wilson, Li Ding. Bioinformatics 2009
745
16

Detection and interpretation of genomic structural variation in mammals.
Ira M Hall, Aaron R Quinlan. Methods Mol Biol 2012
8
25


Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.
James R Priest, Santhosh Girirajan, Tiffany H Vu, Aaron Olson, Evan E Eichler, Michael A Portman. Am J Med Genet A 2012
30
16

Computational techniques for human genome resequencing using mated gapped reads.
Paolo Carnevali, Jonathan Baccash, Aaron L Halpern, Igor Nazarenko, Geoffrey B Nilsen, Krishna P Pant, Jessica C Ebert, Anushka Brownley, Matt Morenzoni, Vitali Karpinchyk,[...]. J Comput Biol 2012
71
16

Copy-number variants in neurodevelopmental disorders: promises and challenges.
Alison K Merikangas, Aiden P Corvin, Louise Gallagher. Trends Genet 2009
87
16

A SNP discovery method to assess variant allele probability from next-generation resequencing data.
Yufeng Shen, Zhengzheng Wan, Cristian Coarfa, Rafal Drabek, Lei Chen, Elizabeth A Ostrowski, Yue Liu, George M Weinstock, David A Wheeler, Richard A Gibbs,[...]. Genome Res 2010
118
16

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
773
16

Rare mutations in XRCC2 increase the risk of breast cancer.
D J Park, F Lesueur, T Nguyen-Dumont, M Pertesi, F Odefrey, F Hammet, S L Neuhausen, E M John, I L Andrulis, M B Terry,[...]. Am J Hum Genet 2012
115
16

More on the sequencing of the human genome.
Robert H Waterston, Eric S Lander, John E Sulston. Proc Natl Acad Sci U S A 2003
20
16

Detection of nonneutral substitution rates on mammalian phylogenies.
Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
16


De novo assembly of short sequence reads.
Konrad Paszkiewicz, David J Studholme. Brief Bioinform 2010
91
16


Dynamic evolution of V1R putative pheromone receptors between Mus musculus and Mus spretus.
Vanessa C Kurzweil, Mike Getman, Eric D Green, Robert P Lane. BMC Genomics 2009
15
16

Automatic annotation of protein function.
Alfonso Valencia. Curr Opin Struct Biol 2005
72
16

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
16

A human genome structural variation sequencing resource reveals insights into mutational mechanisms.
Jeffrey M Kidd, Tina Graves, Tera L Newman, Robert Fulton, Hillary S Hayden, Maika Malig, Joelle Kallicki, Rajinder Kaul, Richard K Wilson, Evan E Eichler. Cell 2010
187
16


Transforming clinical microbiology with bacterial genome sequencing.
Xavier Didelot, Rory Bowden, Daniel J Wilson, Tim E A Peto, Derrick W Crook. Nat Rev Genet 2012
407
16


Exome sequencing of prostate cancer supports the hypothesis of independent tumour origins.
Johan Lindberg, Daniel Klevebring, Wennuan Liu, Mårten Neiman, Jianfeng Xu, Peter Wiklund, Fredrik Wiklund, Ian G Mills, Lars Egevad, Henrik Grönberg. Eur Urol 2013
105
16

New approaches to molecular diagnosis.
Bruce R Korf, Heidi L Rehm. JAMA 2013
79
16


LOVD v.2.0: the next generation in gene variant databases.
Ivo F A C Fokkema, Peter E M Taschner, Gerard C P Schaafsma, J Celli, Jeroen F J Laros, Johan T den Dunnen. Hum Mutat 2011
556
16

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer.
Katie Snape, Elise Ruark, Patrick Tarpey, Anthony Renwick, Clare Turnbull, Sheila Seal, Anne Murray, Sandra Hanks, Jenny Douglas, Michael R Stratton,[...]. Breast Cancer Res Treat 2012
36
16

Old can be new again: HAPPY whole genome sequencing, mapping and assembly.
Zhihua Jiang, Daniel S Rokhsar, Richard M Harland. Int J Biol Sci 2009
13
16

Identification of genetic variants using bar-coded multiplexed sequencing.
David W Craig, John V Pearson, Szabolcs Szelinger, Aswin Sekar, Margot Redman, Jason J Corneveaux, Traci L Pawlowski, Trisha Laub, Gary Nunn, Dietrich A Stephan,[...]. Nat Methods 2008
212
16

Genome interpretation and assembly-recent progress and next steps.
Shawn Baker, Anika Joecker, George Church, Michael Snyder, John West, Steven Salzberg, Elizabeth Worthey, Todd Smith, Jun Wang, Jeffrey G Reid. Nat Biotechnol 2012
6
33


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.