Ankita Patel

Ankita Patel

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Ankita Patel

Publications by authors named "Ankita Patel"

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Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly.

Eur J Med Genet 2019 Jun 22;62(6):103531. Epub 2018 Aug 22.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Texas Children Hospital, Houston, TX, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2018.08.012DOI Listing
June 2019

Aripiprazole and Delusional Disorder.

J Psychiatr Pract 2019 Mar;25(2):132-134

IANNUZZI, PATEL, and STEWART: Department of Psychiatry, James A Haley VA Hospital, University of South Florida College of Medicine, Tampa, FL.

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http://dx.doi.org/10.1097/PRA.0000000000000368DOI Listing
March 2019

Phase 2 Study of Cyclophosphamide, Etoposide, and Estramustine in Patients With Castration-Resistant Prostate Cancer.

Clin Genitourin Cancer 2018 12 28;16(6):473-481. Epub 2018 Jun 28.

Division of Hematology/Oncology, Morsani School of Medicine, University of South Florida, Tampa, FL.

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http://dx.doi.org/10.1016/j.clgc.2018.06.007DOI Listing
December 2018

Evaluating dendritic cells as an in vitro screening tool for immunotherapeutic formulations.

J Immunol Methods 2018 08 23;459:55-62. Epub 2018 May 23.

McWhorter School of Pharmacy, Samford University, 800 Lakeshore Dr, Birmingham, AL 35229, United States. Electronic address:

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http://dx.doi.org/10.1016/j.jim.2018.05.005DOI Listing
August 2018

The importance of phase analysis in multiexon copy number variation detected by aCGH in autosomal recessive disorder loci.

Am J Med Genet A 2017 Sep 20;173(9):2485-2488. Epub 2017 Jun 20.

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

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http://dx.doi.org/10.1002/ajmg.a.38328DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240332PMC
September 2017

Autoimmune Haemolytic Anaemia-A Spectrum of Presentation in Children.

J Clin Diagn Res 2017 Sep 1;11(9):SR01-SR02. Epub 2017 Sep 1.

Senior Resident, Department of Paediatrics, Chacha Nehru Bal Chikitsalaya, New Delhi, India.

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http://dx.doi.org/10.7860/JCDR/2017/27895.10646DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713823PMC
September 2017

Delayed Treatment Response in a Neonate with Multisystem Langerhans Cell Histiocytosis Case report and review of literature.

Sultan Qaboos Univ Med J 2017 May 20;17(2):e225-e228. Epub 2017 Jun 20.

Department of Pediatrics, Chacha Nehru Bal Chikitsalya, New Delhi, India.

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http://dx.doi.org/10.18295/squmj.2016.17.02.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488827PMC
May 2017

Universal Prenatal Chromosomal Microarray Analysis: Additive Value and Clinical Dilemmas in Fetuses with a Normal Karyotype.

Am J Perinatol 2017 03 17;34(4):340-348. Epub 2016 Aug 17.

Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Lenox-Hill Hospital, New York, New York.

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http://dx.doi.org/10.1055/s-0036-1586501DOI Listing
March 2017

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.

J Pediatr Genet 2017 Mar 30;6(1):42-50. Epub 2016 May 30.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States; Baylor Miraca Genetics Laboratories, Baylor College of Medicine, Houston, Texas, United States.

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http://dx.doi.org/10.1055/s-0036-1584306DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288005PMC
March 2017

An Organismal CNV Mutator Phenotype Restricted to Early Human Development.

Cell 2017 02;168(5):830-842.e7

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2017.01.037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407901PMC
February 2017

Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.

Genet Med 2016 10 25;18(10):1052-5. Epub 2016 Feb 25.

Department of Obstetrics and Gynecology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.

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http://dx.doi.org/10.1038/gim.2015.216DOI Listing
October 2016

Mohr-Claussen Syndrome: A Rare Case.

J Clin Diagn Res 2016 Oct 1;10(10):ZJ01-ZJ02. Epub 2016 Oct 1.

Intern, MP Dental College and Hospital , Vadodara, Gujarat, India .

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http://dx.doi.org/10.7860/JCDR/2016/22381.8635DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121831PMC
October 2016

Application of DNA Microarray to Clinical Diagnostics.

Methods Mol Biol 2016 ;1368:111-32

Medical Genetics Laboratories, Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.

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http://dx.doi.org/10.1007/978-1-4939-3136-1_9DOI Listing
September 2016

De Novo Thrombotic Microangiopathy Immediately After Kidney Transplant in Patients Without Apparent Risk Factors.

Exp Clin Transplant 2016 Apr 30;14(2):230-4. Epub 2015 May 30.

Kraftsow Division of Nephrology, Einstein Medical Center Philadelphia, Philadelphia, PA 19141, USA.

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http://dx.doi.org/10.6002/ect.2014.0089DOI Listing
April 2016

Triploidy mosaicism (45,X/68,XX) in an infant presenting with failure to thrive.

Am J Med Genet A 2016 Mar 14;170(3):694-8. Epub 2015 Nov 14.

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

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http://dx.doi.org/10.1002/ajmg.a.37469DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760878PMC
March 2016

Phenotypic and molecular characterization of focal dermal hypoplasia in 18 individuals.

Am J Med Genet C Semin Med Genet 2016 Mar 7;172C(1):9-20. Epub 2016 Feb 7.

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http://doi.wiley.com/10.1002/ajmg.c.31473
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http://dx.doi.org/10.1002/ajmg.c.31473DOI Listing
March 2016

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.

Am J Med Genet A 2015 Nov 31;167A(11):2664-73. Epub 2015 Jul 31.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia.

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http://dx.doi.org/10.1002/ajmg.a.37269DOI Listing
November 2015

Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.

Hum Mol Genet 2015 Jul 23;24(14):4061-77. Epub 2015 Apr 23.

Department of Molecular & Human Genetics, Department of Pediatrics and Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA, Texas Children's Hospital, Houston, TX 77030, USA and

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http://dx.doi.org/10.1093/hmg/ddv146DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476451PMC
July 2015

Homozygous inv(11)(q21q23) and MLL gene rearrangement in two patients with myeloid neoplasms.

Int J Clin Exp Pathol 2014 15;7(6):3196-201. Epub 2014 May 15.

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

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4097224PMC
May 2015

Genitourinary defects associated with genomic deletions in 2p15 encompassing OTX1.

PLoS One 2014 9;9(9):e107028. Epub 2014 Sep 9.

Center for Reproductive Medicine, Baylor College of Medicine, Houston, Texas, United States of America; Scott Department of Urology, Baylor College of Medicine, Houston, Texas, United States of America; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0107028PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159299PMC
May 2015

Accurate description of DNA-based noninvasive prenatal screening.

N Engl J Med 2015 Apr 1;372(17):1675-7. Epub 2015 Apr 1.

Baylor College of Medicine, Houston, TX.

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http://dx.doi.org/10.1056/NEJMc1412222DOI Listing
April 2015

Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review.

BMC Med Genet 2015 Mar 14;16:12. Epub 2015 Mar 14.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS NAB 2015, Houston, TX, 77030, U.S.A.

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http://dx.doi.org/10.1186/s12881-015-0157-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422130PMC
March 2015

Variable levels of tissue mosaicism can confound the interpretation of chromosomal microarray results from peripheral blood.

Eur J Med Genet 2014 May-Jun;57(6):264-6. Epub 2014 Mar 15.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Medicine, Baylor College of Medicine, Houston, TX, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.03.001DOI Listing
February 2015

Mucoadhesive microspheres containing anti-hypertensive agent: formulation and characterization.

Curr Drug Deliv 2014 ;11(3):322-31

A.R. College of Pharmacy & G.H. Patel Institute of Pharmacy, Vallabh Vidyanagar, Anand, Gujarat, India.

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January 2015

Flavonoid rich fraction of Punica granatum improves early diabetic nephropathy by ameliorating proteinuria and disturbed glucose homeostasis in experimental animals.

Pharm Biol 2015 Jan 7;53(1):61-71. Epub 2014 Oct 7.

Department of Pharmacology , PES's Modern College of Pharmacy, Nigdi, Pune, Maharashtra , India.

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http://dx.doi.org/10.3109/13880209.2014.910533DOI Listing
January 2015

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination.

BMC Biol 2014 Sep 23;12:74. Epub 2014 Sep 23.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Rm ABBR-R809, Houston, TX, USA.

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http://dx.doi.org/10.1186/s12915-014-0074-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195946PMC
September 2014

Heterozygous deletion of exons 18 and 19 of IGF1R in an individual with short stature.

Clin Dysmorphol 2014 Jul;23(3):98-100

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

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http://dx.doi.org/10.1097/MCD.0000000000000032DOI Listing
July 2014

Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue.

Reprod Biol Endocrinol 2014 Mar 3;12:19. Epub 2014 Mar 3.

Program for Early and Recurrent Pregnancy Loss (PEARL), Department of Obstetrics, Gynecology & Women's Health, Albert Einstein College of Medicine, 1301 Morris Park Avenue, Price Building, Room 474, Bronx, NY 10461, USA.

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http://dx.doi.org/10.1186/1477-7827-12-19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996014PMC
March 2014

Obstructed or malpositioned urethral catheter induced acute kidney injury.

Case Rep Nephrol 2012 11;2012:731502. Epub 2012 Oct 11.

Department of Medicine, SUNY Downstate Medical Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.

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http://dx.doi.org/10.1155/2012/731502DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914162PMC
February 2014

A preliminary investigation of depression and kidney functioning in patients with chronic kidney disease.

Nephron Clin Pract 2012 1;122(3-4):139-45. Epub 2013 Jun 1.

Department of Psychiatry and Behavioral Science, SUNY Downstate Medical Center, New York, NY 11203, USA.

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http://dx.doi.org/10.1159/000349940DOI Listing
February 2014

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.

Epilepsia 2014 Feb 24;55(2):e6-12. Epub 2013 Dec 24.

Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1111/epi.12489DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195652PMC
February 2014

SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.

Am J Med Genet B Neuropsychiatr Genet 2013 Dec 6;162B(8):832-40. Epub 2013 Sep 6.

Institutes of Biomedical Sciences, Children's Hospital and MOE Key Laboratory of Contemporary Anthropology, Fudan University, Shanghai, China; Department of Laboratory Medicine, Boston Children's Hospital, Boston, Massachusetts.

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http://dx.doi.org/10.1002/ajmg.b.32187DOI Listing
December 2013

Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.

Am J Med Genet A 2013 Dec 2;161A(12):2953-63. Epub 2013 Oct 2.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas; Department of Pediatrics-Hematology-Oncology, Baylor College of Medicine and Texas Children's Cancer Center, Houston, Texas.

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http://dx.doi.org/10.1002/ajmg.a.35886DOI Listing
December 2013

DNA from dead cancer cells induces TLR9-mediated invasion and inflammation in living cancer cells.

Breast Cancer Res Treat 2013 Dec 10;142(3):477-87. Epub 2013 Nov 10.

Division of Hematology-Oncology, Department of Medicine, University of Alabama at Birmingham, SHEL 514, 1825 University Blvd, Birmingham, AL, 35294-3300, USA.

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http://dx.doi.org/10.1007/s10549-013-2762-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238912PMC
December 2013

SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties.

Nature 2013 Nov 23;503(7474):72-7. Epub 2013 Oct 23.

1] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA [2] Howard Hughes Medical Institute, Baylor College of Medicine, Houston, Texas 77030, USA [3] Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1038/nature12630DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923348PMC
November 2013

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Am J Hum Genet 2013 Aug 27;93(2):197-210. Epub 2013 Jun 27.

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

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http://www.cell.com/cms/attachment/2024885301/2044552963/mmc
Web Search
http://linkinghub.elsevier.com/retrieve/pii/S000292971300269
Publisher Site
http://dx.doi.org/10.1016/j.ajhg.2013.05.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738832PMC
August 2013

Engineered DNA ligases with improved activities in vitro.

Protein Eng Des Sel 2013 Jul 10;26(7):471-8. Epub 2013 Jun 10.

Institute of Natural Sciences, Massey University, Auckland 0632, New Zealand.

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http://dx.doi.org/10.1093/protein/gzt024DOI Listing
July 2013

Peritoneal dialysis should not be the first choice for renal replacement therapy in the elderly.

Semin Dial 2012 Nov-Dec;25(6):671-4. Epub 2012 Oct 19.

Renal Disease Division, State University of New York, Downstate Medical Center, Brooklyn, New York 11203, USA.

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http://doi.wiley.com/10.1111/sdi.12012
Publisher Site
http://dx.doi.org/10.1111/sdi.12012DOI Listing
May 2013

Preparation of chorionic villus samples for metaphase chromosome analysis and chromosomal microarray analysis.

Curr Protoc Hum Genet 2012 Oct;Chapter 8:Unit8.3

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

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http://dx.doi.org/10.1002/0471142905.hg0803s75DOI Listing
October 2012

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

Prenat Diagn 2012 Apr;32(4):351-61

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

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http://dx.doi.org/10.1002/pd.3861DOI Listing
April 2012

Formulation and evaluation of bilayer tablet by using melt granulation technique for treatment of diabetes mellitus.

J Pharm Bioallied Sci 2012 Mar;4(Suppl 1):S37-9

B.S.Patel Pharmacy College, Saffrony Institute of technology, Linch, Mehsana.

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http://dx.doi.org/10.4103/0975-7406.94135DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467847PMC
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

VACTERL association and mitochondrial dysfunction.

Birth Defects Res A Clin Mol Teratol 2011 Mar 9;91(3):192-4. Epub 2011 Feb 9.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA. solomonb@ mail.nih.gov

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http://dx.doi.org/10.1002/bdra.20768DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500509PMC
March 2011