Publications by authors named "Samarth Bhatt"

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Dehydroepiandrosterone at birth: Response to stress and relation to demographic, pregnancy and delivery factors.
Hayley S Kamin, Samarth S Bhatt, Connie J Mulligan, Darlene A Kertes

J Neuroendocrinol· October 2020

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Children's Relationship With Their Pet Dogs and Genotype Predict Child-Pet Interaction in an Experimental Setting.
Darlene A Kertes, Nathan Hall, Samarth S Bhatt

Front Psychol· September 2018

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Putting a finger on the problem: Finger stick blood draw and immunization at the well-child exam elicit a cortisol response to stress among one-year-old children.
Darlene A Kertes, Hayley S Kamin, Jingwen Liu, Samarth S Bhatt, Maria Kelly

Psychoneuroendocrinology· July 2018

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methylation in mothers and newborns is associated with maternal exposure to war trauma.
Darlene A Kertes, Samarth S Bhatt, Hayley S Kamin, David A Hughes, Nicole C Rodney

Clin Epigenetics· April 2018

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Effect of Pet Dogs on Children's Perceived Stress and Cortisol Stress Response.
Darlene A Kertes, Jingwen Liu, Nathan J Hall, Natalie A Hadad, Clive D L Wynne, Samarth S Bhatt

Soc Dev· May 2017

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Prenatal Maternal Stress Predicts Methylation of Genes Regulating the Hypothalamic-Pituitary-Adrenocortical System in Mothers and Newborns in the Democratic Republic of Congo.
Darlene A Kertes, Hayley S Kamin, David A Hughes, Nicole C Rodney, Samarth Bhatt

Child Dev· December 2016

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A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia.
Abdulsamad Wafa, Faten Moassass, Thomas Liehr, Samarth Bhatt, Abdulmunim Aljapawe

Mol Cytogenet· December 2016

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Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability.
Valerie Maduro, Barbara N Pusey, Praveen F Cherukuri, Paul Atkins, Christèle du Souich, Samarth S Bhatt

Orphanet J Rare Dis· May 2016

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Chromosomes in a genome-wise order: evidence for metaphase architecture.
Anja Weise, Samarth Bhatt, Katja Piaszinski, Nadezda Kosyakova, Xiaobo Fan

Mol Cytogenet· April 2016

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Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish.
Kathrin Reichwald, Andreas Petzold, Philipp Koch, Bryan R Downie, Nils Hartmann, Samarth S Bhatt

Cell· December 2015

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Application of BAC-probes to visualize copy number variants (CNVs).
Anja Weise, Moneeb A K Othman, Samarth Bhatt, Sharon Löhmer, Thomas Liehr

Methods Mol Biol· May 2015

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A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.
Laura Rodríguez, Samarth S Bhatt, Mónica García-Castro, Ana Plasencia, Joaquín Fernández-Toral

Gene· February 2014

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Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by indocyanine green in breast adenocarcinoma MCF-7 cells.
Mona A M Abo-Zeid, Thomas Liehr, Sherien M El-Daly, Amira M Gamal-Eldeen, Michael Glei, Samarth Bhatt

Photodiagnosis Photodyn Ther· May 2013

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Heteromorphic variants of chromosome 9.
Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, Marina Manvelyan, Isabella Simonyan, Samarth Bhatt

Mol Cytogenet· April 2013

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A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.
Daniela Ribeiro Ney-Garcia, Társis Paiva Vieira, Thomas Liehr, Samarth Bhatt, Mariana Tavares de Souza

Blood Cells Mol Dis· February 2013

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Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?
Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, Ahmed B Hamid, Samarth Bhatt

Chromosome Res· October 2012

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Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, Samarth Bhatt

J Histochem Cytochem· May 2012

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A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
Amanda Faria de Figueiredo, Tarsis Paiva Vieira, Thomas Liehr, Samarth Bhatt, Mariana Tavares de Souza

Leuk Res· April 2012

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Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia.
Daniela R Ney-Garcia, Thomas Liehr, Samarth Bhatt, Mariana T de Souza, Roberto R Capela de Matos

Leuk Lymphoma· February 2012

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Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
Paweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, Srirangan Sampath, Samarth S Bhatt

Hum Mutat· January 2012

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An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype.
Daniela Rn Garcia, Samarth Bhatt, Marina Manvelyan, Mariana T de Souza, Renata Binato

Mol Cytogenet· September 2011

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A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia.
Amanda Faria De Figueiredo, Thomas Liehr, Samarth Bhatt, Renata Binato, Mariana Tavares De Souza

Leuk Lymphoma· August 2011

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The human genome puzzle - the role of copy number variation in somatic mosaicism.
Hasmik Mkrtchyan, Madeleine Gross, Sophie Hinreiner, Anna Polytiko, Marina Manvelyan, Samarth Bhatt

Curr Genomics· September 2010

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A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes.
Marwan Shinawi, Christian P Schaaf, Samarth S Bhatt, Zhilian Xia, Ankita Patel

Nat Genet· December 2009

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Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
Lisenka E L M Vissers, Samarth S Bhatt, Irene M Janssen, Zhilian Xia, Seema R Lalani

Hum Mol Genet· October 2009

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