Literature DB >> 25570068

Ensemble learning for the detection of facial dysmorphology.

Qian Zhao, Naoufel Werghi, Kazunori Okada, Kenneth Rosenbaum, Marshall Summar, Marius George Linguraru.   

Abstract

Down syndrome is the most common chromosomal condition that presents characteristic facial morphology and texture patterns. The early detection of Down syndrome through an automatic, non-invasive and simple way is desirable and critical to provide the best health management to newborns. In this study, we propose such a computer-aided diagnosis system for Down syndrome from photography based on facial analysis with ensemble learning. First, geometric and texture facial features are extracted based on automatically located facial landmarks, followed by feature fusion and selection. Then multiple classifiers (i.e. support vector machines, random forests and linear discriminant analysis) are adopted to identify patients with Down syndrome. An accurate and reliable decision is finally achieved by optimally combining the outputs of these individual classifiers via ensemble learning that captures both the shared and complementary information from different classifiers. The best performance was achieved by using the median ensemble rule with 0.967 accuracy, 0.977 precision and 0.933 recall.

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Mesh:

Year:  2014        PMID: 25570068     DOI: 10.1109/EMBC.2014.6943700

Source DB:  PubMed          Journal:  Conf Proc IEEE Eng Med Biol Soc        ISSN: 1557-170X


  4 in total

1.  Cornelia de Lange syndrome in diverse populations.

Authors:  Leah Dowsett; Antonio R Porras; Paul Kruszka; Brandon Davis; Tommy Hu; Engela Honey; Eben Badoe; Meow-Keong Thong; Eyby Leon; Katta M Girisha; Anju Shukla; Shalini S Nayak; Vorasuk Shotelersuk; Andre Megarbane; Shubha Phadke; Nirmala D Sirisena; Vajira H W Dissanayake; Carlos R Ferreira; Monisha S Kisling; Pranoot Tanpaiboon; Annette Uwineza; Leon Mutesa; Cedrik Tekendo-Ngongang; Ambroise Wonkam; Karen Fieggen; Leticia Cassimiro Batista; Danilo Moretti-Ferreira; Roger E Stevenson; Eloise J Prijoles; David Everman; Kate Clarkson; Jessica Worthington; Virginia Kimonis; Fuki Hisama; Carol Crowe; Paul Wong; Kisha Johnson; Robin D Clark; Lynne Bird; Diane Masser-Frye; Marie McDonald; Patrick Willems; Elizabeth Roeder; Sulgana Saitta; Kwame Anyane-Yeoba; Laurie Demmer; Naoki Hamajima; Zornitza Stark; Greta Gillies; Louanne Hudgins; Usha Dave; Stavit Shalev; Victoria Siu; Ann Ades; Holly Dubbs; Sarah Raible; Maninder Kaur; Emanuela Salzano; Laird Jackson; Matthew Deardorff; Antonie Kline; Marshall Summar; Maximilian Muenke; Marius George Linguraru; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2019-01-06       Impact factor: 2.802

2.  22q11.2 deletion syndrome in diverse populations.

Authors:  Paul Kruszka; Yonit A Addissie; Daniel E McGinn; Antonio R Porras; Elijah Biggs; Matthew Share; T Blaine Crowley; Brian H Y Chung; Gary T K Mok; Christopher C Y Mak; Premala Muthukumarasamy; Meow-Keong Thong; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; L B Lahiru Prabodha; Rupesh Mishra; Vorasuk Shotelersuk; Ekanem Nsikak Ekure; Ogochukwu Jidechukwu Sokunbi; Nnenna Kalu; Carlos R Ferreira; Jordann-Mishael Duncan; Siddaramappa Jagdish Patil; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Annette Uwineza; Leon Mutesa; Angélica Moresco; María Gabriela Obregon; Antonio Richieri-Costa; Vera L Gil-da-Silva-Lopes; Adebowale A Adeyemo; Marshall Summar; Elaine H Zackai; Donna M McDonald-McGinn; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2017-04       Impact factor: 2.802

3.  Noonan syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Yonit A Addissie; Angélica Moresco; Sofia Medrano; Gary T K Mok; Gordon K C Leung; Cedrik Tekendo-Ngongang; Annette Uwineza; Meow-Keong Thong; Premala Muthukumarasamy; Engela Honey; Ekanem N Ekure; Ogochukwu J Sokunbi; Nnenna Kalu; Kelly L Jones; Julie D Kaplan; Omar A Abdul-Rahman; Lisa M Vincent; Amber Love; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Anju Shukla; Katta M Girisha; Siddaramappa J Patil; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Eva Klein-Zighelboim; Bertha E Gallardo Jugo; Miguel Chávez Pastor; Hugo H Abarca-Barriga; Steven A Skinner; Eloise J Prijoles; Eben Badoe; Ashleigh D Gill; Vorasuk Shotelersuk; Patroula Smpokou; Monisha S Kisling; Carlos R Ferreira; Leon Mutesa; Andre Megarbane; Antonie D Kline; Amy Kimball; Emmy Okello; Peter Lwabi; Twalib Aliku; Emmanuel Tenywa; Nonglak Boonchooduang; Pranoot Tanpaiboon; Antonio Richieri-Costa; Ambroise Wonkam; Brian H Y Chung; Roger E Stevenson; Marshall Summar; Kausik Mandal; Shubha R Phadke; María G Obregon; Marius G Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2017-07-27       Impact factor: 2.802

4.  Williams-Beuren syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Deise Helena de Souza; Angélica Moresco; Victoria Huckstadt; Ashleigh D Gill; Alec P Boyle; Tommy Hu; Yonit A Addissie; Gary T K Mok; Cedrik Tekendo-Ngongang; Karen Fieggen; Eloise J Prijoles; Pranoot Tanpaiboon; Engela Honey; Ho-Ming Luk; Ivan F M Lo; Meow-Keong Thong; Premala Muthukumarasamy; Kelly L Jones; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Laila Bouguenouch; Anju Shukla; Katta M Girisha; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Monisha S Kisling; Carlos R Ferreira; María Beatriz de Herreros; Ni-Chung Lee; Saumya S Jamuar; Angeline Lai; Ee Shien Tan; Jiin Ying Lim; Cham Breana Wen-Min; Neerja Gupta; Stephanie Lotz-Esquivel; Ramsés Badilla-Porras; Dalia Farouk Hussen; Mona O El Ruby; Engy A Ashaat; Siddaramappa J Patil; Leah Dowsett; Alison Eaton; A Micheil Innes; Vorasuk Shotelersuk; Ëben Badoe; Ambroise Wonkam; María Gabriela Obregon; Brian H Y Chung; Milana Trubnykova; Jorge La Serna; Bertha Elena Gallardo Jugo; Miguel Chávez Pastor; Hugo Hernán Abarca Barriga; Andre Megarbane; Beth A Kozel; Mieke M van Haelst; Roger E Stevenson; Marshall Summar; A Adebowale Adeyemo; Colleen A Morris; Danilo Moretti-Ferreira; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.578

  4 in total

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