Laura Winchester, Jiannis Ragoussis. Methods Mol Biol 2012
Times Cited: 2
Times Cited: 2
Times Cited
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Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization.
M Daniely, A Aviram-Goldring, G Barkai, B Goldman. Hum Reprod 1998
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Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
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Routine pre-evacuation ultrasound diagnosis of hydatidiform mole: experience of more than 1000 cases from a regional referral center.
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The placenta in multiple pregnancy: outstanding issues.
K Benirschke, E Masliah. Reprod Fertil Dev 2001
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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
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The syndromes of hydatidiform mole. II. Morphologic evolution of the complete and partial mole.
A E Szulman, U Surti. Am J Obstet Gynecol 1978
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The role of morphology in combination with ploidy analysis in characterizing early gestational abortion.
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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
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Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.
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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
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Hydatidiform mole: two entities. A morphologic and cytogenetic study with some clinical consideration.
P Vassilakos, G Riotton, T Kajii. Am J Obstet Gynecol 1977
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Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.
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Short tandem repeat typing technologies used in human identity testing.
John M Butler. Biotechniques 2007
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Molecular genotyping of hydatidiform moles: analytic validation of a multiplex short tandem repeat assay.
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Kathleen M Murphy, Thomas G McConnell, Michael J Hafez, Russell Vang, Brigitte M Ronnett. J Mol Diagn 2009
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Comparison of fluorescence in situ hybridization, p57 immunostaining, flow cytometry, and digital image analysis for diagnosing molar and nonmolar products of conception.
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Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations.
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Choriocarcinoma and partial hydatidiform moles.
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Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
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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
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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
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Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.
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Björn Menten, Katrien Swerts, Barbara Delle Chiaie, Sandra Janssens, Karen Buysse, Jan Philippé, Frank Speleman. BMC Med Genet 2009
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Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
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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
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Histomorphometric features of hydatidiform moles in early pregnancy: relationship to detectability by ultrasound examination.
D J Fowler, I Lindsay, M J Seckl, N J Sebire. Ultrasound Obstet Gynecol 2007
D J Fowler, I Lindsay, M J Seckl, N J Sebire. Ultrasound Obstet Gynecol 2007
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Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.
M V Zaragoza, U Surti, R W Redline, E Millie, A Chakravarti, T J Hassold. Am J Hum Genet 2000
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Epidemiology of gestational trophoblastic diseases.
Stephen James Steigrad. Best Pract Res Clin Obstet Gynaecol 2003
Stephen James Steigrad. Best Pract Res Clin Obstet Gynaecol 2003
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Diagnosis and subclassification of hydatidiform moles using p57 immunohistochemistry and molecular genotyping: validation and prospective analysis in routine and consultation practice settings with development of an algorithmic approach.
Thomas G McConnell, Kathleen M Murphy, Michael Hafez, Russell Vang, Brigitte M Ronnett. Am J Surg Pathol 2009
Thomas G McConnell, Kathleen M Murphy, Michael Hafez, Russell Vang, Brigitte M Ronnett. Am J Surg Pathol 2009
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Enhancements to the ADMIXTURE algorithm for individual ancestry estimation.
David H Alexander, Kenneth Lange. BMC Bioinformatics 2011
David H Alexander, Kenneth Lange. BMC Bioinformatics 2011
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Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data.
Soon-Young Kim, Ji-Hong Kim, Yeun-Jun Chung. Genomics Inform 2012
Soon-Young Kim, Ji-Hong Kim, Yeun-Jun Chung. Genomics Inform 2012
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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
Miguel Alves-Ferreira, Marlene Quintas, Jorge Sequeiros, Alda Sousa, José Pereira-Monteiro, Isabel Alonso, João Luís Neto, Carolina Lemos. J Headache Pain 2021
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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
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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
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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
Ying Zhou, Sharon R Browning, Brian L Browning. Am J Hum Genet 2020
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Inference of population structure using dense haplotype data.
Daniel John Lawson, Garrett Hellenthal, Simon Myers, Daniel Falush. PLoS Genet 2012
Daniel John Lawson, Garrett Hellenthal, Simon Myers, Daniel Falush. PLoS Genet 2012
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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
Muhammad Imran Qadeer, Ali Amar, Yung-Yu Huang, Eli Min, Hanga Galfalvy, Shahida Hasnain, J John Mann. Sci Rep 2021
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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
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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
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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
Andrew E Dellinger, Seang-Mei Saw, Liang K Goh, Mark Seielstad, Terri L Young, Yi-Ju Li. Nucleic Acids Res 2010
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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
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Rapid adaptation to malaria facilitated by admixture in the human population of Cabo Verde.
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Iman Hamid, Katharine L Korunes, Sandra Beleza, Amy Goldberg. Elife 2021
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PCAdmix: principal components-based assignment of ancestry along each chromosome in individuals with admixed ancestry from two or more populations.
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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
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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
Xihan Guo, Xueqin Dai, Tao Zhou, Han Wang, Juan Ni, Jinglun Xue, Xu Wang. Hum Genet 2020
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Structural Variability, Expression Profile, and Pharmacogenetic Properties of TMPRSS2 Gene as a Potential Target for COVID-19 Therapy.
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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
Carl A Anderson, Fredrik H Pettersson, Geraldine M Clarke, Lon R Cardon, Andrew P Morris, Krina T Zondervan. Nat Protoc 2010
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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
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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
Timothy Shin Heng Mak, Robert Milan Porsch, Shing Wan Choi, Xueya Zhou, Pak Chung Sham. Genet Epidemiol 2017
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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
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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
Ali Pazokitoroudi, Alec M Chiu, Kathryn S Burch, Bogdan Pasaniuc, Sriram Sankararaman. Am J Hum Genet 2021
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