Publications by authors named "Patricia Hixson"

22Publications

Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination.

Authors:
Michał Startek Przemyslaw Szafranski Tomasz Gambin Ian M Campbell Patricia Hixson Chad A Shaw Paweł Stankiewicz Anna Gambin

Nucleic Acids Res 2015 Feb 22;43(4):2188-98. Epub 2015 Jan 22.

Faculty of Mathematics, Informatics, and Mechanics, University of Warsaw, 2 Banacha street, 02-097 Warsaw, Poland Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawińskiego street, 02-106 Warsaw, Poland

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February 2015

Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications.

Authors:
Przemyslaw Szafranski Sailaja Golla Weihong Jin Ping Fang Patricia Hixson Reuben Matalon Daniel Kinney Hans-Georg Bock William Craigen Janice L Smith Weimin Bi Ankita Patel Sau Wai Cheung Carlos A Bacino Paweł Stankiewicz

Eur J Hum Genet 2015 Jul 15;23(7):915-21. Epub 2014 Oct 15.

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

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July 2015

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

Authors:
Ian M Campbell Tomasz Gambin Piotr Dittwald Christine R Beck Andrey Shuvarikov Patricia Hixson Ankita Patel Anna Gambin Chad A Shaw Jill A Rosenfeld Paweł Stankiewicz

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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September 2014

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

Authors:
Sirisak Chanprasert Janice L Smith Patricia Hixson Ankita Patel Seema R Lalani

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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July 2014

Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive cases.

Authors:
Justin Pham Chad Shaw Amber Pursley Patricia Hixson Srirangan Sampath Erin Roney Tomasz Gambin Sung-Hae L Kang Weimin Bi Seema Lalani Carlos Bacino James R Lupski Pawel Stankiewicz Ankita Patel Sau-Wai Cheung

Eur J Hum Genet 2014 Aug 8;22(8):969-78. Epub 2014 Jan 8.

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

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August 2014

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

Authors:
Wojciech Wiszniewski Jill V Hunter Neil A Hanchard Jason R Willer Chad Shaw Qi Tian Anna Illner Xueqing Wang Sau W Cheung Ankita Patel Ian M Campbell Violet Gelowani Patricia Hixson Audrey R Ester Mahshid S Azamian Lorraine Potocki Gladys Zapata Patricia P Hernandez Melissa B Ramocki Regie L P Santos-Cortez Gao Wang Michele K York Monica J Justice Zili D Chu Patricia I Bader Lisa Omo-Griffith Nirupama S Madduri Gunter Scharer Heather P Crawford Pattamawadee Yanatatsaneejit Anna Eifert Jeffery Kerr Carlos A Bacino Adiaha I A Franklin Robin P Goin-Kochel Gayle Simpson Ladonna Immken Muhammad E Haque Marija Stosic Misti D Williams Thomas M Morgan Sumit Pruthi Reed Omary Simeon A Boyadjiev Kay K Win Aye Thida Matthew Hurles Martin Lloyd Hibberd Chiea Chuen Khor Nguyen Van Vinh Chau Thomas E Gallagher Apiwat Mutirangura Pawel Stankiewicz Arthur L Beaudet Mirjana Maletic-Savatic Jill A Rosenfeld Lisa G Shaffer Erica E Davis John W Belmont Sarah Dunstan Cameron P Simmons Penelope E Bonnen Suzanne M Leal Nicholas Katsanis James R Lupski Seema R Lalani

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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August 2013

Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.

Authors:
Joanna Wiszniewska Weimin Bi Chad Shaw Pawel Stankiewicz Sung-Hae L Kang Amber N Pursley Seema Lalani Patricia Hixson Tomasz Gambin Chun-hui Tsai Hans-Georg Bock Maria Descartes Frank J Probst Fernando Scaglia Arthur L Beaudet James R Lupski Christine Eng Sau Wai Cheung Carlos Bacino Ankita Patel

Eur J Hum Genet 2014 Jan 22;22(1):79-87. Epub 2013 May 22.

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

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January 2014

Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles.

Authors:
Philip M Boone Ian M Campbell Brett C Baggett Zachry T Soens Mitchell M Rao Patricia M Hixson Ankita Patel Weimin Bi Sau Wai Cheung Seema R Lalani Arthur L Beaudet Pawel Stankiewicz Chad A Shaw James R Lupski

Genome Res 2013 Sep 16;23(9):1383-94. Epub 2013 May 16.

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

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September 2013

Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay.

Authors:
Jens Witsch Przemyslaw Szafranski Chun-An Chen LaDonna Immken Gayle Simpson Patel Patricia Hixson Sau Wai Cheung Pawel Stankiewicz Christian P Schaaf

Eur J Hum Genet 2013 Nov 13;21(11):1304-7. Epub 2013 Mar 13.

Department of Neurology, Charité University Medicine, Campus Virchow Klinikum, Berlin, Germany.

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November 2013

A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14.

Authors:
Lindsay C Burrage Tanya N Eble Patricia M Hixson Erin K Roney Sau W Cheung Luis M Franco

Am J Med Genet A 2013 Apr 26;161A(4):841-4. Epub 2013 Feb 26.

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

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April 2013

Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?

Authors:
Weimin Bi Caroline Borgan Amber N Pursley Patricia Hixson Chad A Shaw Carlos A Bacino Seema R Lalani Ankita Patel Pawel Stankiewicz James R Lupski Arthur L Beaudet Sau Wai Cheung

Genet Med 2013 Jun 13;15(6):450-7. Epub 2012 Dec 13.

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

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June 2013

Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities.

Authors:
Seema R Lalani Chad Shaw Xueqing Wang Ankita Patel Lance W Patterson Katarzyna Kolodziejska Przemyslaw Szafranski Zhishuo Ou Qi Tian Sung-Hae L Kang Amina Jinnah Sophia Ali Aamir Malik Patricia Hixson Lorraine Potocki James R Lupski Pawel Stankiewicz Carlos A Bacino Brian Dawson Arthur L Beaudet Fatima M Boricha Runako Whittaker Chumei Li Stephanie M Ware Sau Wai Cheung Daniel J Penny John Lynn Jefferies John W Belmont

Eur J Hum Genet 2013 Feb 29;21(2):173-81. Epub 2012 Aug 29.

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

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February 2013

Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function.

Authors:
Sandesh C S Nagamani Ayelet Erez Frank J Probst Patricia Bader Patricia Evans Linda A Baker Ping Fang Terry Bertin Patricia Hixson Pawel Stankiewicz David Nelson Ankita Patel Sau Wai Cheung

Neurogenetics 2012 Nov 14;13(4):333-9. Epub 2012 Aug 14.

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

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November 2012

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage-fusion-bridge for telomere stabilization.

Authors:
Svetlana A Yatsenko Patricia Hixson Erin K Roney Daryl A Scott Christian P Schaaf Yu-tze Ng Robbin Palmer Richard B Fisher Ankita Patel Sau Wai Cheung James R Lupski

Hum Genet 2012 Dec 14;131(12):1895-910. Epub 2012 Aug 14.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room 604B, Houston, TX 77030, USA.

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December 2012

Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1A.

Authors:
Ian M Campbell Svetlana A Yatsenko Patricia Hixson Tyler Reimschisel Matthew Thomas William Wilson Usha Dayal James W Wheless Amy Crunk Cynthia Curry Nicole Parkinson Leona Fishman James J Riviello Malgorzata J M Nowaczyk Susan Zeesman Jill A Rosenfeld Bassem A Bejjani Lisa G Shaffer Sau Wai Cheung James R Lupski Pawel Stankiewicz Fernando Scaglia

Genet Med 2012 Oct 21;14(10):868-76. Epub 2012 Jun 21.

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

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October 2012

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

Authors:
Amy Breman Amber N Pursley Patricia Hixson Weimin Bi Patricia Ward Carlos A Bacino Chad Shaw James R Lupski Arthur Beaudet Ankita Patel Sau W Cheung Ignatia Van den Veyver

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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April 2012

Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44.

Authors:
Sandesh C Sreenath Nagamani Ayelet Erez Carolyn Bay Anjana Pettigrew Seema R Lalani Kristin Herman Brett H Graham Malgorzata Jm Nowaczyk Monica Proud William J Craigen Bobbi Hopkins Beth Kozel Katie Plunkett Patricia Hixson Pawel Stankiewicz Ankita Patel Sau Wai Cheung

Eur J Hum Genet 2012 Feb 21;20(2):176-9. Epub 2011 Sep 21.

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

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February 2012

Phenotypic manifestations of copy number variation in chromosome 16p13.11.

Authors:
Sandesh C Sreenath Nagamani Ayelet Erez Patricia Bader Seema R Lalani Daryl A Scott Fernando Scaglia Sharon E Plon Chun-Hui Tsai Tyler Reimschisel Elizabeth Roeder Amy D Malphrus Patricia A Eng Patricia M Hixson Sung-Hae L Kang Pawel Stankiewicz Ankita Patel Sau Wai Cheung

Eur J Hum Genet 2011 Mar 8;19(3):280-6. Epub 2010 Dec 8.

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

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March 2011

Detection of clinically relevant exonic copy-number changes by array CGH.

Authors:
Philip M Boone Carlos A Bacino Chad A Shaw Patricia A Eng Patricia M Hixson Amber N Pursley Sung-Hae L Kang Yaping Yang Joanna Wiszniewska Beata A Nowakowska Daniela del Gaudio Zhilian Xia Gayle Simpson-Patel LaDonna L Immken James B Gibson Anne C-H Tsai Jennifer A Bowers Tyler E Reimschisel Christian P Schaaf Lorraine Potocki Fernando Scaglia Tomasz Gambin Maciej Sykulski Magdalena Bartnik Katarzyna Derwinska Barbara Wisniowiecka-Kowalnik Seema R Lalani Frank J Probst Weimin Bi Arthur L Beaudet Ankita Patel James R Lupski Sau Wai Cheung Pawel Stankiewicz

Hum Mutat 2010 Dec 2;31(12):1326-42. Epub 2010 Nov 2.

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

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December 2010

Array comparative genomic hybridization detects chromosomal abnormalities in hematological cancers that are not detected by conventional cytogenetics.

Authors:
Lina Shao Sung-Hae L Kang Jian Li Patricia Hixson Jesalyn Taylor Svetlana A Yatsenko Chad A Shaw Aleksandar Milosavljevic Chung-Che Chang Sau Wai Cheung Ankita Patel

J Mol Diagn 2010 Sep 19;12(5):670-9. Epub 2010 Aug 19.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77021-2039, USA.

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September 2010