Publications by authors named "Amanda Collins"

28Publications

Negative affect interference and fear of happiness are independently associated with depressive symptoms.

J Clin Psychol 2020 Oct 20. Epub 2020 Oct 20.

Department of Psychology, Mississippi State University, Starkville, Mississippi, USA.

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http://dx.doi.org/10.1002/jclp.23066DOI Listing
October 2020

Exomphalos without other prenatally detected anomalies: Perinatal outcomes from 22 years of population-based data.

Prenat Diagn 2020 Jul 8. Epub 2020 Jul 8.

Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.

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http://dx.doi.org/10.1002/pd.5782DOI Listing
July 2020

Conceptualizing anhedonias and implications for depression treatments.

Psychol Res Behav Manag 2019 13;12:325-335. Epub 2019 May 13.

Department of Psychology, Mississippi State University, Starkville, MS 39762, USA,

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http://dx.doi.org/10.2147/PRBM.S159260DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521843PMC
May 2019

Population representation among anatomical donors and the implication for medical student education.

Clin Anat 2018 Mar 6;31(2):250-258. Epub 2017 Dec 6.

Department of Radiology, University of Massachusetts Medical School, Worcester, Massachusetts.

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http://dx.doi.org/10.1002/ca.23013DOI Listing
March 2018

Inherited 2q23.1 microdeletions involving the locus.

Mol Genet Genomic Med 2017 Sep 8;5(5):608-613. Epub 2017 Aug 8.

North East Thames Regional Genetics ServiceGreat Ormond Street HospitalLondonWC1N 3JHUK.

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http://dx.doi.org/10.1002/mgg3.316DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606852PMC
September 2017

Gallstone ileus.

J Emerg Med 2013 Feb 21;44(2):e277-8. Epub 2012 Aug 21.

Department of Emergency Medicine and Department of Radiology, University of Massachusetts Medical School, Worcester, MA 01655, USA.

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http://dx.doi.org/10.1016/j.jemermed.2012.06.020DOI Listing
February 2013

Transmitted deletions of medial 5p and learning difficulties; does the cadherin cluster only become penetrant when flanking genes are deleted?

Am J Med Genet A 2011 Nov 30;155A(11):2807-15. Epub 2011 Sep 30.

Human Genetics Division, Southampton University School of Medicine, Southampton General Hospital, Southampton, UK.

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http://dx.doi.org/10.1002/ajmg.a.34241DOI Listing
November 2011

Aplasia cutis congenita, terminal limb defects and periventricular leukomalacia in one sibling with minor findings in the other-probable autosomal recessive Adams-Oliver Syndrome.

Eur J Med Genet 2009 Jul-Aug;52(4):234-8. Epub 2009 May 4.

Sheffield Clinical Genetics Service, Sheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield S10 2TH, UK.

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http://linkinghub.elsevier.com/retrieve/pii/S176972120900055
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http://dx.doi.org/10.1016/j.ejmg.2009.04.005DOI Listing
November 2009

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.

N Engl J Med 2008 Oct 10;359(16):1685-99. Epub 2008 Sep 10.

University of Washington School of Medicine, Seattle 98195, USA.

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http://dx.doi.org/10.1056/NEJMoa0805384DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2703742PMC
October 2008

Early detection: a survey of secondary school teachers' knowledge about psychosis.

Early Interv Psychiatry 2008 May;2(2):90-7

Greenwich Early Intervention Team, Greenwich, UK.

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http://dx.doi.org/10.1111/j.1751-7893.2008.00063.xDOI Listing
May 2008

Early detection: a survey of secondary school teachers' knowledge about psychosis.

Early Interv Psychiatry 2008 May;2(2):90-7

Greenwich Early Intervention Team, Greenwich, UK.

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http://dx.doi.org/10.1111/j.1751-7893.2008.00063.xDOI Listing
May 2008

Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.

Mol Biotechnol 2007 Feb;35(2):135-40

National Genetics Reference Laboratory (Wessex), Salisbury Hospital NHS Trust, Salisbury, Wiltshire, SP2 8BJ.

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http://dx.doi.org/10.1007/BF02686108DOI Listing
February 2007

Surgical correction of entropion and excess upper eyelid skin in congenital cutis laxa: a case report.

Orbit 1999 Mar;18(1):53-58

Salisbury District Hospital, Salisbury, Wiltshire, England, U.K.

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http://dx.doi.org/10.1076/orbi.18.1.53.2722DOI Listing
March 1999

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.

Am J Hum Genet 2002 Feb 3;70(2):547-55. Epub 2002 Jan 3.

Molecular Medicine Unit, Institute of Child Health, London, United Kingdom.

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http://dx.doi.org/10.1086/338921DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC384929PMC
February 2002