Publications by authors named "Trilochan Sahoo"

63Publications

Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly.

Clin Dysmorphol 2020 Oct 7. Epub 2020 Oct 7.

Institute of Human Genetics, University Hospital Magdeburg Leipziger Str. 44 39120 Magdeburg Germany.

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http://dx.doi.org/10.1097/MCD.0000000000000351DOI Listing
October 2020

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.

Am J Hum Genet 2018 11;103(5):740-751

Department of Human Genetics, McGill University Health Centre, Montréal, QC H4A 3J1, Canada; Department of Obstetrics and Gynecology, McGill University Health Centre, Montréal, QC H4A 3J1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.10.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218808PMC
November 2018

Expanding noninvasive prenatal testing to include microdeletions and segmental aneuploidy: cause for concern?

Genet Med 2016 Mar 21;18(3):275-6. Epub 2016 Jan 21.

Combimatrix Molecular Diagnostics, Irvine, California, USA.

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http://dx.doi.org/10.1038/gim.2015.196DOI Listing
March 2016

Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.

Am J Med Genet A 2015 Apr 3;167A(4):910-3. Epub 2015 Mar 3.

Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.36962DOI Listing
April 2015

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.

Genet Med 2015 Mar 7;17(3):234-6. Epub 2014 Aug 7.

Cytogenetics Laboratory, Quest Diagnostics Nichols Institute, San Juan Capistrano, California, USA.

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http://dx.doi.org/10.1038/gim.2014.92DOI Listing
March 2015

Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.

Am J Med Genet A 2013 Jul 17;161A(7):1695-701. Epub 2013 May 17.

Cytogenetics Laboratory, Quest Diagnostics Nichols Institute, San Juan Capistrano, CA 92690, USA.

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http://dx.doi.org/10.1002/ajmg.a.35939DOI Listing
July 2013

Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.

Mol Cytogenet 2012 Jul 9;5(1):31. Epub 2012 Jul 9.

Department of Pathology and Laboratory Medicine, Weill Cornell Medical College/NewYork-Presbyterian Hospital, New York, NY, USA.

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http://dx.doi.org/10.1186/1755-8166-5-31DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419606PMC
July 2012

BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative disease.

Mol Cytogenet 2012 May 1;5(1):23. Epub 2012 May 1.

Cytogenetics, Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA 92675, USA.

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http://dx.doi.org/10.1186/1755-8166-5-23DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467166PMC
May 2012

Localized surface plasmon enhanced quantum efficiency of InGaN/GaN quantum wells by Ag/SiO2 nanoparticles.

Opt Express 2012 Jan;20(3):2116-23

School of Advanced Materials Engineering and Research Center of Advanced Materials Development, Chonbuk National University, Jeonju 561-756, South Korea.

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http://dx.doi.org/10.1364/OE.20.002116DOI Listing
January 2012

Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay.

Am J Med Genet A 2011 Dec 7;155A(12):3110-5. Epub 2011 Nov 7.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, Washington, USA.

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http://doi.wiley.com/10.1002/ajmg.a.34345
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http://dx.doi.org/10.1002/ajmg.a.34345DOI Listing
December 2011

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.

Eur J Hum Genet 2012 Mar 2;20(3):283-90. Epub 2011 Nov 2.

Department of Psychiatry, University of Florida, Gainesville, FL, USA.

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http://dx.doi.org/10.1038/ejhg.2011.187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283188PMC
March 2012

11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity.

Am J Med Genet A 2011 Jun 12;155A(6):1272-80. Epub 2011 May 12.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.33878DOI Listing
June 2011

The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.

Autism Res 2009 Apr;2(2):98-108

Department of Molecular and Human Genetics, Baylor College of Medicine, Texas Children's Hospital, 1102 Bates Street, FC148, Houston, TX 77030, USA.

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http://doi.wiley.com/10.1002/aur.70
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http://dx.doi.org/10.1002/aur.70DOI Listing
April 2009

A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.

Am J Med Genet A 2009 Mar;149A(3):396-402

Division of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor, Michigan 48109-5241, USA.

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http://deepblue.lib.umich.edu/bitstream/handle/2027.42/61892
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http://doi.wiley.com/10.1002/ajmg.a.32691
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http://dx.doi.org/10.1002/ajmg.a.32691DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872113PMC
March 2009

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.

Prenat Diagn 2008 Oct;28(10):943-9

Medical Genetics Laboratories, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://doi.wiley.com/10.1002/pd.2087
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http://dx.doi.org/10.1002/pd.2087DOI Listing
October 2008

15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.

Am J Med Genet A 2008 Aug;146A(15):1933-41

Department of Molecular and Human Genetics, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas 77030, USA.

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http://doi.wiley.com/10.1002/ajmg.a.32324
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http://dx.doi.org/10.1002/ajmg.a.32324DOI Listing
August 2008

Atypical cases of Angelman syndrome.

Am J Med Genet A 2006 Nov;140(21):2361-4

Division of Genetics and Metabolism, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1002/ajmg.a.31481DOI Listing
November 2006

Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity.

J Pediatr 2006 Aug;149(2):192-8

Department of Pediatrics and the Center for Mammalian Genetics, University of Florida, College of Medicine, Gainesville, Florida 32610-0296, USA.

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http://dx.doi.org/10.1016/j.jpeds.2006.04.013DOI Listing
August 2006

Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.

Am J Med Genet A 2005 Dec;139A(2):106-13

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.31000DOI Listing
December 2005

Creatine metabolism in combined methylmalonic aciduria and homocystinuria.

Ann Neurol 2005 Apr;57(4):557-60

Unit of Biochemical Genetics, Department of Pediatrics, University of Vienna Children's Hospital, Vienna, Austria.

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http://dx.doi.org/10.1002/ana.20419DOI Listing
April 2005

A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.

Am J Med Genet A 2005 Feb;133A(1):93-8

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

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http://dx.doi.org/10.1002/ajmg.a.30535DOI Listing
February 2005

Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].

Am J Med Genet A 2004 Jul;128A(1):72-7

Department of Molecular and Human Genetics, Baylor College of Medicine, and Texas Children's Hospital, Clinical Care Center, 6621 Fannin, Houston, TX 77030, USA.

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http://doi.wiley.com/10.1002/ajmg.a.30094
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http://dx.doi.org/10.1002/ajmg.a.30094DOI Listing
July 2004