A citation-based method for searching scientific literature

Laura Winchester, Jiannis Ragoussis. Methods Mol Biol 2012
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity



Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
Caroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, Joris Robert Vermeesch. Genet Med 2009
65
50


The placenta in multiple pregnancy: outstanding issues.
K Benirschke, E Masliah. Reprod Fertil Dev 2001
20
50

Histopathological diagnosis of partial and complete hydatidiform mole in the first trimester of pregnancy.
Neil J Sebire, Rosemary A Fisher, Helene C Rees. Pediatr Dev Pathol 2003
68
50


The role of morphology in combination with ploidy analysis in characterizing early gestational abortion.
Isabella Grinschgl, Sebastian Mannweiler, Margit Holzapfel-Bauer, Ulrich Pferschy, Gerald Hoefler, Barbara Guertl. Virchows Arch 2013
6
50

Diagnosis of hydatidiform moles by polymorphic deletion probe fluorescence in situ hybridization.
Sarah Chiang, Ladan Fazlollahi, Anhthu Nguyen, Rebecca A Betensky, Drucilla J Roberts, A John Iafrate. J Mol Diagn 2011
13
50

Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.
B Lomax, S Tang, E Separovic, D Phillips, E Hillard, T Thomson, D K Kalousek. Am J Hum Genet 2000
106
50

Multiplex short tandem repeat DNA analysis confirms the accuracy of p57(KIP2) immunostaining in the diagnosis of complete hydatidiform mole.
Dorota A Popiolek, Herman Yee, Khush Mittal, Luis Chiriboga, Mechthild K Prinz, Theresa A Caragine, Zoran M Budimlija. Hum Pathol 2006
42
50


Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.
Y-X Zhang, Y-P Zhang, Y Gu, F-J Guan, S-L Li, J-S Xie, Y Shen, B-L Wu, W Ju, E C Jenkins,[...]. Clin Genet 2009
53
50


Molecular genotyping of hydatidiform moles: analytic validation of a multiplex short tandem repeat assay.
Kathleen M Murphy, Thomas G McConnell, Michael J Hafez, Russell Vang, Brigitte M Ronnett. J Mol Diagn 2009
55
50


Comparison of fluorescence in situ hybridization, p57 immunostaining, flow cytometry, and digital image analysis for diagnosing molar and nonmolar products of conception.
Benjamin R Kipp, Rhett P Ketterling, Trynda N Oberg, Margot A Cousin, Amy M Plagge, Anne E Wiktor, Johnita M Ihrke, Cecelia H Meyers, William G Morice, Kevin C Halling,[...]. Am J Clin Pathol 2010
18
50


Choriocarcinoma and partial hydatidiform moles.
M J Seckl, R A Fisher, G Salerno, H Rees, F J Paradinas, M Foskett, E S Newlands. Lancet 2000
217
50

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
Laura K Conlin, Brian D Thiel, Carsten G Bonnemann, Livija Medne, Linda M Ernst, Elaine H Zackai, Matthew A Deardorff, Ian D Krantz, Hakon Hakonarson, Nancy B Spinner. Hum Mol Genet 2010
276
50

The accuracy of first trimester ultrasound in the diagnosis of hydatidiform mole.
E Kirk, A T Papageorghiou, G Condous, C Bottomley, T Bourne. Ultrasound Obstet Gynecol 2007
49
50

Diagnostic utility of microsatellite genotyping for molar pregnancy testing.
Larissa V Furtado, Christian N Paxton, Mohamed A Jama, Sheryl R Tripp, Andrew R Wilson, Elaine Lyon, Elke A Jarboe, Harshwardhan M Thaker, Katherine B Geiersbach. Arch Pathol Lab Med 2013
22
50

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.
Björn Menten, Katrien Swerts, Barbara Delle Chiaie, Sandra Janssens, Karen Buysse, Jan Philippé, Frank Speleman. BMC Med Genet 2009
52
50

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Eleanor Wheeler, Ni Huang, Elena G Bochukova, Julia M Keogh, Sarah Lindsay, Sumedha Garg, Elana Henning, Hannah Blackburn, Ruth J F Loos, Nick J Wareham,[...]. Nat Genet 2013
202
50

Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions.
Vaidehi Jobanputra, Antonio Sobrino, Ann Kinney, Jennie Kline, Dorothy Warburton. Hum Reprod 2002
49
50


Gestational trophoblastic disease.
Michael J Seckl, Neil J Sebire, Ross S Berkowitz. Lancet 2010
443
50


Epidemiology of gestational trophoblastic diseases.
Stephen James Steigrad. Best Pract Res Clin Obstet Gynaecol 2003
83
50


Enhancements to the ADMIXTURE algorithm for individual ancestry estimation.
David H Alexander, Kenneth Lange. BMC Bioinformatics 2011
393
50


A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study.
Miguel Alves-Ferreira, Marlene Quintas, Jorge Sequeiros, Alda Sousa, José Pereira-Monteiro, Isabel Alonso, João Luís Neto, Carolina Lemos. J Headache Pain 2021
2
50

Polygenic risk scoring to assess genetic overlap and protective factors influencing posttraumatic stress, depression, and chronic pain after motor vehicle collision trauma.
Jarred J Lobo, Samuel A McLean, Andrew S Tungate, David A Peak, Robert A Swor, Niels K Rathlev, Phyllis L Hendry, Sarah D Linnstaedt. Transl Psychiatry 2021
3
50

The role of polygenic risk and susceptibility genes in breast cancer over the course of life.
Nina Mars, Elisabeth Widén, Sini Kerminen, Tuomo Meretoja, Matti Pirinen, Pietro Della Briotta Parolo, Priit Palta, Aarno Palotie, Jaakko Kaprio, Heikki Joensuu,[...]. Nat Commun 2020
20
50

A Fast and Simple Method for Detecting Identity-by-Descent Segments in Large-Scale Data.
Ying Zhou, Sharon R Browning, Brian L Browning. Am J Hum Genet 2020
25
50

Inference of population structure using dense haplotype data.
Daniel John Lawson, Garrett Hellenthal, Simon Myers, Daniel Falush. PLoS Genet 2012
529
50

Association of serotonin system-related genes with homicidal behavior and criminal aggression in a prison population of Pakistani Origin.
Muhammad Imran Qadeer, Ali Amar, Yung-Yu Huang, Eli Min, Hanga Galfalvy, Shahida Hasnain, J John Mann. Sci Rep 2021
4
50

Ancestral haplotype reconstruction in endogamous populations using identity-by-descent.
Kelly Finke, Michael Kourakos, Gabriela Brown, Huyen Trang Dang, Shi Jie Samuel Tan, Yuval B Simons, Shweta Ramdas, Alejandro A Schäffer, Rachel L Kember, Maja Bućan,[...]. PLoS Comput Biol 2021
2
50

Sensitive detection of chromosomal segments of distinct ancestry in admixed populations.
Alkes L Price, Arti Tandon, Nick Patterson, Kathleen C Barnes, Nicholas Rafaels, Ingo Ruczinski, Terri H Beaty, Rasika Mathias, David Reich, Simon Myers. PLoS Genet 2009
340
50

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays.
Andrew E Dellinger, Seang-Mei Saw, Liang K Goh, Mark Seielstad, Terri L Young, Yi-Ju Li. Nucleic Acids Res 2010
83
50

PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data.
Chris D Greenman, Graham Bignell, Adam Butler, Sarah Edkins, Jon Hinton, Dave Beare, Sajani Swamy, Thomas Santarius, Lina Chen, Sara Widaa,[...]. Biostatistics 2010
141
50

Rapid adaptation to malaria facilitated by admixture in the human population of Cabo Verde.
Iman Hamid, Katharine L Korunes, Sandra Beleza, Amy Goldberg. Elife 2021
13
50

PCAdmix: principal components-based assignment of ancestry along each chromosome in individuals with admixed ancestry from two or more populations.
Abra Brisbin, Katarzyna Bryc, Jake Byrnes, Fouad Zakharia, Larsson Omberg, Jeremiah Degenhardt, Andrew Reynolds, Harry Ostrer, Jason G Mezey, Carlos D Bustamante. Hum Biol 2012
106
50

Mosaic loss of human Y chromosome: what, how and why.
Xihan Guo, Xueqin Dai, Tao Zhou, Han Wang, Juan Ni, Jinglun Xue, Xu Wang. Hum Genet 2020
27
50

Structural Variability, Expression Profile, and Pharmacogenetic Properties of TMPRSS2 Gene as a Potential Target for COVID-19 Therapy.
Aleksei Zarubin, Vadim Stepanov, Anton Markov, Nikita Kolesnikov, Andrey Marusin, Irina Khitrinskaya, Maria Swarovskaya, Sergey Litvinov, Natalia Ekomasova, Murat Dzhaubermezov,[...]. Genes (Basel) 2020
15
50

Data quality control in genetic case-control association studies.
Carl A Anderson, Fredrik H Pettersson, Geraldine M Clarke, Lon R Cardon, Andrew P Morris, Krina T Zondervan. Nat Protoc 2010
661
50

RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference.
Brian K Maples, Simon Gravel, Eimear E Kenny, Carlos D Bustamante. Am J Hum Genet 2013
315
50

Polygenic scores via penalized regression on summary statistics.
Timothy Shin Heng Mak, Robert Milan Porsch, Shing Wan Choi, Xueya Zhou, Pak Chung Sham. Genet Epidemiol 2017
86
50

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Andrew R Harper, Anuj Goel, Christopher Grace, Kate L Thomson, Steffen E Petersen, Xiao Xu, Adam Waring, Elizabeth Ormondroyd, Christopher M Kramer, Carolyn Y Ho,[...]. Nat Genet 2021
40
50

Quantifying the contribution of dominance deviation effects to complex trait variation in biobank-scale data.
Ali Pazokitoroudi, Alec M Chiu, Kathryn S Burch, Bogdan Pasaniuc, Sriram Sankararaman. Am J Hum Genet 2021
6
50


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.