Syed H Zaidi

Syed H Zaidi

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Syed H Zaidi

Syed H Zaidi

Publications by authors named "Syed H Zaidi"

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Discovery of common and rare genetic risk variants for colorectal cancer.

Authors:
Jeroen R Huyghe Stephanie A Bien Tabitha A Harrison Hyun Min Kang Sai Chen Stephanie L Schmit David V Conti Conghui Qu Jihyoun Jeon Christopher K Edlund Peyton Greenside Michael Wainberg Fredrick R Schumacher Joshua D Smith David M Levine Sarah C Nelson Nasa A Sinnott-Armstrong Demetrius Albanes M Henar Alonso Kristin Anderson Coral Arnau-Collell Volker Arndt Christina Bamia Barbara L Banbury John A Baron Sonja I Berndt Stéphane Bézieau D Timothy Bishop Juergen Boehm Heiner Boeing Hermann Brenner Stefanie Brezina Stephan Buch Daniel D Buchanan Andrea Burnett-Hartman Katja Butterbach Bette J Caan Peter T Campbell Christopher S Carlson Sergi Castellví-Bel Andrew T Chan Jenny Chang-Claude Stephen J Chanock Maria-Dolores Chirlaque Sang Hee Cho Charles M Connolly Amanda J Cross Katarina Cuk Keith R Curtis Albert de la Chapelle Kimberly F Doheny David Duggan Douglas F Easton Sjoerd G Elias Faye Elliott Dallas R English Edith J M Feskens Jane C Figueiredo Rocky Fischer Liesel M FitzGerald David Forman Manish Gala Steven Gallinger W James Gauderman Graham G Giles Elizabeth Gillanders Jian Gong Phyllis J Goodman William M Grady John S Grove Andrea Gsur Marc J Gunter Robert W Haile Jochen Hampe Heather Hampel Sophia Harlid Richard B Hayes Philipp Hofer Michael Hoffmeister John L Hopper Wan-Ling Hsu Wen-Yi Huang Thomas J Hudson David J Hunter Gemma Ibañez-Sanz Gregory E Idos Roxann Ingersoll Rebecca D Jackson Eric J Jacobs Mark A Jenkins Amit D Joshi Corinne E Joshu Temitope O Keku Timothy J Key Hyeong Rok Kim Emiko Kobayashi Laurence N Kolonel Charles Kooperberg Tilman Kühn Sébastien Küry Sun-Seog Kweon Susanna C Larsson Cecelia A Laurie Loic Le Marchand Suzanne M Leal Soo Chin Lee Flavio Lejbkowicz Mathieu Lemire Christopher I Li Li Li Wolfgang Lieb Yi Lin Annika Lindblom Noralane M Lindor Hua Ling Tin L Louie Satu Männistö Sanford D Markowitz Vicente Martín Giovanna Masala Caroline E McNeil Marilena Melas Roger L Milne Lorena Moreno Neil Murphy Robin Myte Alessio Naccarati Polly A Newcomb Kenneth Offit Shuji Ogino N Charlotte Onland-Moret Barbara Pardini Patrick S Parfrey Rachel Pearlman Vittorio Perduca Paul D P Pharoah Mila Pinchev Elizabeth A Platz Ross L Prentice Elizabeth Pugh Leon Raskin Gad Rennert Hedy S Rennert Elio Riboli Miguel Rodríguez-Barranco Jane Romm Lori C Sakoda Clemens Schafmayer Robert E Schoen Daniela Seminara Mitul Shah Tameka Shelford Min-Ho Shin Katerina Shulman Sabina Sieri Martha L Slattery Melissa C Southey Zsofia K Stadler Christa Stegmaier Yu-Ru Su Catherine M Tangen Stephen N Thibodeau Duncan C Thomas Sushma S Thomas Amanda E Toland Antonia Trichopoulou Cornelia M Ulrich David J Van Den Berg Franzel J B van Duijnhoven Bethany Van Guelpen Henk van Kranen Joseph Vijai Kala Visvanathan Pavel Vodicka Ludmila Vodickova Veronika Vymetalkova Korbinian Weigl Stephanie J Weinstein Emily White Aung Ko Win C Roland Wolf Alicja Wolk Michael O Woods Anna H Wu Syed H Zaidi Brent W Zanke Qing Zhang Wei Zheng Peter C Scacheri John D Potter Michael C Bassik Anshul Kundaje Graham Casey Victor Moreno Goncalo R Abecasis Deborah A Nickerson Stephen B Gruber Li Hsu Ulrike Peters

Nat Genet 2019 01 3;51(1):76-87. Epub 2018 Dec 3.

Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

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http://www.nature.com/articles/s41588-018-0286-6
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http://dx.doi.org/10.1038/s41588-018-0286-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358437PMC
January 2019

The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: An illustration.

Genomics 2015 Dec 11;106(6):340-7. Epub 2015 Sep 11.

Department of Surgery, University Health Network, Toronto, Ontario M5G 2C4, Canada; Prosserman Centre for Health Research, Lunenfeld-Tanenbaum Research Institute, Toronto, Ontario M5G 1X5, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ygeno.2015.09.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722538PMC
December 2015

Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds.

Ann Saudi Med 2014 Mar-Apr;34(2):107-14

Dr. Muhammad Faiyaz-Ul-Haque, Department of Pathology,, College of Medicine,, King Khaled University Hospital,, King Saud University, T: 966-11-4699377, F: +966-11-4672462,

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http://dx.doi.org/10.5144/0256-4947.2014.107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074860PMC
November 2015

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.

Nat Commun 2015 Feb 26;6:6326. Epub 2015 Feb 26.

1] Ontario Institute for Cancer Research, Toronto, Ontario, Canada M5G 0A3 [2] Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada M5S 1A1 [3] Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A1.

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http://dx.doi.org/10.1038/ncomms7326DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351585PMC
February 2015

Enhanced proliferation and altered calcium handling in RGS2-deficient vascular smooth muscle cells.

J Recept Signal Transduct Res 2014 Dec 20;34(6):476-83. Epub 2014 May 20.

Division of Experimental Therapeutics, Toronto General Research Institute , University Health Network, Toronto, Ontario , Canada and.

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http://www.tandfonline.com/doi/full/10.3109/10799893.2014.92
Publisher Site
http://dx.doi.org/10.3109/10799893.2014.920393DOI Listing
December 2014

A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations.

Eur J Pediatr 2010 Jun 25;169(6):661-6. Epub 2010 Feb 25.

Department of Pathology and Laboratory Medicine, Molecular Genetics Laboratory, King Faisal Specialist Hospital & Research Centre, PO Box 3354, MBC#10, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1007/s00431-010-1150-6DOI Listing
June 2010

Novel and recurrent mutations in the C1NH gene of Arab patients affected with hereditary angioedema.

Int Arch Allergy Immunol 2010 15;151(2):149-54. Epub 2009 Sep 15.

Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1159/000236005DOI Listing
February 2010

Growth differentiation factor 5 regulates cardiac repair after myocardial infarction.

J Am Coll Cardiol 2010 Jan;55(2):135-43

Division of Cardiology, University Health Network, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.jacc.2009.08.041DOI Listing
January 2010

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.

Eur J Pediatr 2009 Dec 4;168(12):1467-71. Epub 2009 Mar 4.

Department of Pathology, Molecular Genetics Laboratory, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1007/s00431-009-0953-9DOI Listing
December 2009

A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin.

Eur J Pediatr 2009 Jul 26;168(7):867-70. Epub 2008 Sep 26.

Division of Cardiology, Department of Medicine, University Health Network & University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1007/s00431-008-0839-2DOI Listing
July 2009

Some rare presentations of hydatid cysts: two case reports.

Authors:
Syed H Zaidi

Cases J 2009 Jan 18;2(1):62. Epub 2009 Jan 18.

Department of Surgery, PNS Rahat Hospital, Karsaz, Karachi, Pakistan.

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http://dx.doi.org/10.1186/1757-1626-2-62DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651114PMC
January 2009

Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5.

J Bone Miner Metab 2008 1;26(6):648-52. Epub 2008 Nov 1.

Molecular Genetics Laboratory, Department of Pathology & Laboratory Medicine, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, MBC #10, Riyadh, 11211, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1007/s00774-008-0853-5DOI Listing
December 2008

Gene transfer of prostaglandin synthase maintains patency of the newborn lamb arterial duct.

Pediatr Res 2005 Nov 23;58(5):976-80. Epub 2005 Sep 23.

Department of Pediatrics, Division of Cardiology, Research Institute, University of Toronto, The Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.

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http://dx.doi.org/10.1203/01.PDR.0000182820.20333.2ADOI Listing
November 2005

Elafin-overexpressing mice have improved cardiac function after myocardial infarction.

Am J Physiol Heart Circ Physiol 2004 Jul 23;287(1):H286-92. Epub 2003 Dec 23.

Program in Cardiovascular Research, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Canada.

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http://med.stanford.edu/labs/rabinovitchbland/word-pdf/Ohta%
Web Search
http://ajpheart.physiology.org/cgi/doi/10.1152/ajpheart.0047
Publisher Site
http://dx.doi.org/10.1152/ajpheart.00479.2002DOI Listing
July 2004

Overexpression of the serine elastase inhibitor elafin protects transgenic mice from hypoxic pulmonary hypertension.

Circulation 2002 Jan;105(4):516-21

Cardiovascular Research, Hospital for Sick Children, Department of Pediatrics, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1161/hc0402.102866DOI Listing
January 2002