Jacek Majewski

Jacek Majewski

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Jacek Majewski

Publications by authors named "Jacek Majewski"

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Epigenomic Reordering Induced by Polycomb Loss Drives Oncogenesis but Leads to Therapeutic Vulnerabilities in Malignant Peripheral Nerve Sheath Tumors.

Cancer Res 2019 Jul 21;79(13):3205-3219. Epub 2019 Mar 21.

Department of Biochemistry and Biophysics, and Penn Epigenetics Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1158/0008-5472.CAN-18-3704DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637743PMC
July 2019

Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease.

J Child Neurol 2019 Feb 28;34(2):74-80. Epub 2018 Nov 28.

1 Departments of Neurology and Neurosurgery, Pediatrics and Human Genetics, McGill University, Montreal, Canada.

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http://dx.doi.org/10.1177/0883073818811223DOI Listing
February 2019

Recessive mutation in CD2AP causes focal segmental glomerulosclerosis in humans and mice.

Kidney Int 2019 01 26;95(1):57-61. Epub 2018 Oct 26.

Research Institute, McGill University Health Centre, Montreal, Quebec, Canada; Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00852538183059
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http://dx.doi.org/10.1016/j.kint.2018.08.014DOI Listing
January 2019

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.

Am J Hum Genet 2018 11;103(5):740-751

Department of Human Genetics, McGill University Health Centre, Montréal, QC H4A 3J1, Canada; Department of Obstetrics and Gynecology, McGill University Health Centre, Montréal, QC H4A 3J1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.10.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218808PMC
November 2018

Pacemaker dependency: how should it be defined?

Europace 2018 10;20(10):1708

Department of Electrocardiology, Collegium Medicum, Institute of Cardiology, Jagiellonian University, John Paul II Hospital. Ul. Pradnicka 80, Krakow, Poland.

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http://dx.doi.org/10.1093/europace/euy010DOI Listing
October 2018

ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants.

Am J Hum Genet 2018 10 13;103(4):474-483. Epub 2018 Sep 13.

Department of Human Genetics, McGill University, Montreal, QC H3A 0G1, Canada.

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http://dx.doi.org/10.1016/j.ajhg.2018.08.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174354PMC
October 2018

Humidity Measurement in Carbon Dioxide with Capacitive Humidity Sensors at Low Temperature and Pressure.

Sensors (Basel) 2018 Aug 9;18(8). Epub 2018 Aug 9.

Department of Automation and Metrology, Faculty of Electrical Engineering and Computer Science, Lublin University of Technology, 38A Nadbystrzycka Str., 20-618 Lublin, Poland.

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http://dx.doi.org/10.3390/s18082615DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111965PMC
August 2018

A family segregating lethal neonatal coenzyme Q deficiency caused by mutations in COQ9.

J Inherit Metab Dis 2018 07 20;41(4):719-729. Epub 2018 Mar 20.

Maritime Medical Genetics Service, IWK Health Centre, 5850 University Avenue, P.O. Box 9700, Halifax, NS, B3K 6R8, Canada.

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http://dx.doi.org/10.1007/s10545-017-0122-7DOI Listing
July 2018

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

Eur J Hum Genet 2018 07 25;26(7):1007-1013. Epub 2018 Apr 25.

Department of Human Genetics, McGill University Health Centre, Montreal, QC, Canada.

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http://dx.doi.org/10.1038/s41431-018-0141-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018785PMC
July 2018

H3.1 K36M mutation in a congenital-onset soft tissue neoplasm.

Pediatr Blood Cancer 2017 Dec 16;64(12). Epub 2017 May 16.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.

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http://dx.doi.org/10.1002/pbc.26633DOI Listing
December 2017

Bmp signaling maintains a mesoderm progenitor cell state in the mouse tailbud.

Development 2017 08 13;144(16):2982-2993. Epub 2017 Jul 13.

Goodman Cancer Research Centre and Department of Biochemistry, McGill University, Montreal, Canada H3A 1A3

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http://dx.doi.org/10.1242/dev.149955DOI Listing
August 2017

LoLoPicker: detecting low allelic-fraction variants from low-quality cancer samples.

Oncotarget 2017 Jun;8(23):37032-37040

Department of Human Genetics, McGill University, Montreal, Quebec, Canada.

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http://dx.doi.org/10.18632/oncotarget.16144DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514890PMC
June 2017

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.

Am J Med Genet A 2017 Jun 21;173(6):1611-1619. Epub 2017 Apr 21.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario.

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http://dx.doi.org/10.1002/ajmg.a.38231DOI Listing
June 2017

Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression.

Invest Ophthalmol Vis Sci 2017 03;58(3):1736-1742

Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.

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http://dx.doi.org/10.1167/iovs.16-20864DOI Listing
March 2017

Longitudinal mutational analysis of a cerebellar pilocytic astrocytoma recurring as a ganglioglioma.

Pediatr Blood Cancer 2017 02 8;64(2):275-278. Epub 2016 Oct 8.

Department of Pathology, McGill University Health Centre, Montreal, Canada.

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http://dx.doi.org/10.1002/pbc.26215DOI Listing
February 2017

A novel multisystem disease associated with recessive mutations in the tyrosyl-tRNA synthetase (YARS) gene.

Am J Med Genet A 2017 Jan 15;173(1):126-134. Epub 2016 Sep 15.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37973DOI Listing
January 2017

RMND1-Related Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss-Another Mendelian Mimicker of Congenital Cytomegalovirus Infection.

Pediatr Neurol 2017 01 13;66:59-62. Epub 2016 Sep 13.

Department of Neurology, Children's National Medical Center, Washington, DC; Department of Integrated Systems Biology, George Washington University, Washington, DC; Department of Pediatrics, George Washington University, Washington, DC. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2016.09.003DOI Listing
January 2017

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene.

J Allergy Clin Immunol 2016 12 4;138(6):1681-1689.e8. Epub 2016 Jun 4.

Laboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Biotherapy Clinical Investigation Center, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2016.04.032DOI Listing
December 2016

Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors.

Authors:
Jonathon Torchia Brian Golbourn Shengrui Feng King Ching Ho Patrick Sin-Chan Alexandre Vasiljevic Joseph D Norman Paul Guilhamon Livia Garzia Natalia R Agamez Mei Lu Tiffany S Chan Daniel Picard Pasqualino de Antonellis Dong-Anh Khuong-Quang Aline C Planello Constanze Zeller Dalia Barsyte-Lovejoy Lucie Lafay-Cousin Louis Letourneau Mathieu Bourgey Man Yu Deena M A Gendoo Misko Dzamba Mark Barszczyk Tiago Medina Alexandra N Riemenschneider A Sorana Morrissy Young-Shin Ra Vijay Ramaswamy Marc Remke Christopher P Dunham Stephen Yip Ho-Keung Ng Jian-Qiang Lu Vivek Mehta Steffen Albrecht Jose Pimentel Jennifer A Chan Gino R Somers Claudia C Faria Lucia Roque Maryam Fouladi Lindsey M Hoffman Andrew S Moore Yin Wang Seung Ah Choi Jordan R Hansford Daniel Catchpoole Diane K Birks Nicholas K Foreman Doug Strother Almos Klekner Laszló Bognár Miklós Garami Péter Hauser Tibor Hortobágyi Beverly Wilson Juliette Hukin Anne-Sophie Carret Timothy E Van Meter Eugene I Hwang Amar Gajjar Shih-Hwa Chiou Hideo Nakamura Helen Toledano Iris Fried Daniel Fults Takafumi Wataya Chris Fryer David D Eisenstat Katrin Scheinemann Adam J Fleming Donna L Johnston Jean Michaud Shayna Zelcer Robert Hammond Samina Afzal David A Ramsay Nongnuch Sirachainan Suradej Hongeng Noppadol Larbcharoensub Richard G Grundy Rishi R Lulla Jason R Fangusaro Harriet Druker Ute Bartels Ronald Grant David Malkin C Jane McGlade Theodore Nicolaides Tarik Tihan Joanna Phillips Jacek Majewski Alexandre Montpetit Guillaume Bourque Gary D Bader Alyssa T Reddy G Yancey Gillespie Monika Warmuth-Metz Stefan Rutkowski Uri Tabori Mathieu Lupien Michael Brudno Ulrich Schüller Torsten Pietsch Alexander R Judkins Cynthia E Hawkins Eric Bouffet Seung-Ki Kim Peter B Dirks Michael D Taylor Anat Erdreich-Epstein Cheryl H Arrowsmith Daniel D De Carvalho James T Rutka Nada Jabado Annie Huang

Cancer Cell 2016 Dec;30(6):891-908

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5G0A4, Canada; Department of Paediatrics, University of Toronto, Toronto, ON M5G0A4, Canada; Division of Hematology/Oncology, Hospital for Sick Children, Toronto, ON M5G1X8, Canada; Arthur and Sonia Labatt Brain Tumour Research Centre, Hospital for Sick Children, Toronto, ON M5G1X8, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ccell.2016.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500911PMC
December 2016

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.

CMAJ 2016 Aug 30;188(11):E254-E260. Epub 2016 May 30.

Department of Genetics (Daoud, Luco, Beaulieu, Jarinova, Carson, Nikkel, Graham, Richer, Armour, Boycott, Dyment) and Department of Pediatrics (Bulman, Chakraborty, Geraghty, Lines, Lacaze-Masmonteil), Children's Hospital of Eastern Ontario, Ottawa, Ont.; McGill University (Li, Bareke, Majewski) and Genome Quebec Innovation Centre (Li, Bareke, Majewski), Montréal, Que.

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http://dx.doi.org/10.1503/cmaj.150823DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4978597PMC
August 2016

SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.

Eur J Hum Genet 2016 07 2;24(7):1016-21. Epub 2015 Dec 2.

Neurogenetics of Motion Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.

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http://www.nature.com/doifinder/10.1038/ejhg.2015.240
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http://dx.doi.org/10.1038/ejhg.2015.240DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070891PMC
July 2016

Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia.

Neurogenetics 2016 Apr 26;17(2):137-41. Epub 2016 Feb 26.

Neurogenetics of Motion Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, QC, H3A 2B4, Canada.

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http://dx.doi.org/10.1007/s10048-016-0476-2DOI Listing
April 2016

Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.

Brain 2016 Mar 10;139(Pt 3):e19. Epub 2015 Dec 10.

2 Department of Human Genetics, McGill University, Montreal, Québec, Canada 4 McGill University and Genome Quebec Innovation Centre, Montreal, Québec, Canada

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http://dx.doi.org/10.1093/brain/awv362DOI Listing
March 2016

Candidate DNA repair susceptibility genes identified by exome sequencing in high-risk pancreatic cancer.

Cancer Lett 2016 Jan 3;370(2):302-12. Epub 2015 Nov 3.

Research Institute of the McGill University Health Centre, 1001 Décarie Boulevard, Montreal, QC, Canada H4A 3J1; Goodman Cancer Research Centre, McGill University, 1160 Pine Avenue West, Montreal, QC, Canada H3A 1A3; Program in Cancer Genetics, Departments of Oncology and Human Genetics, Sir Mortimer B. Davis-Jewish General Hospital, McGill University, 3755 Côte-Ste-Catherine Road, Montreal, QC, Canada H3T 1E2. Electronic address:

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http://dx.doi.org/10.1016/j.canlet.2015.10.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725760PMC
January 2016

RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans.

Am J Hum Genet 2015 Dec 19;97(6):862-8. Epub 2015 Nov 19.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.10.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678428PMC
December 2015

Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability.

Hum Mol Genet 2015 Nov 24;24(22):6293-300. Epub 2015 Aug 24.

Children's Hospital of Eastern Ontario Research Institute, Department of Genetics, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, Ontario, Canada K1H 8L1

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http://dx.doi.org/10.1093/hmg/ddv337DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614701PMC
November 2015

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Am J Med Genet A 2015 Nov 26;167A(11):2867. Epub 2015 Aug 26.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37270DOI Listing
November 2015

Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2.

Neuromuscul Disord 2015 Oct 5;25(10):794-9. Epub 2015 Aug 5.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada; Division of Neurology, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2015.07.017DOI Listing
October 2015

Vitamin K antagonists favourably modulate fibrin clot properties in patients with atrial fibrillation as early as after 3days of treatment: Relation to coagulation factors and thrombin generation.

Thromb Res 2015 Oct 16;136(4):832-8. Epub 2015 Aug 16.

Department of Cardiac Surgery, Anaesthesiology and Experimental Cardiology, Institute of Cardiology, Jagiellonian University, Medical College, Krakow, Poland; John Paul II Hospital, Krakow, Poland.

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http://dx.doi.org/10.1016/j.thromres.2015.08.007DOI Listing
October 2015

Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing.

Iran J Public Health 2015 Oct;44(10):1348-52

Dept. of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644579PMC
October 2015

Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy.

Hum Mol Genet 2015 Sep 17;24(18):5109-14. Epub 2015 Jun 17.

ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, Australia.

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http://dx.doi.org/10.1093/hmg/ddv229DOI Listing
September 2015

Leveling the Playing Field in Homozygosity Mapping Using Map Distances.

Ann Hum Genet 2015 Sep 15;79(5):366-372. Epub 2015 Jul 15.

McGill University and Genome Québec Innovation Centre, Montreal, Canada.

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http://dx.doi.org/10.1111/ahg.12125DOI Listing
September 2015

Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene.

Eur J Hum Genet 2015 Jul 5;23(7):990-2. Epub 2014 Nov 5.

Department of Genetics, Children's Hospital of Eastern Ontario, Research Institute and University of Ottawa, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1038/ejhg.2014.236DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463511PMC
July 2015

Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing.

Sci Rep 2015 Jul 6;5:12028. Epub 2015 Jul 6.

Institute of Psychology, Chinese Academy of Sciences, Beijing, China 100101; and Rockefeller University, New York, NY 10065, USA.

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http://dx.doi.org/10.1038/srep12028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155624PMC
July 2015

Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.

J Med Genet 2015 Jun 20;52(6):413-21. Epub 2015 Mar 20.

Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1136/jmedgenet-2015-103018DOI Listing
June 2015

Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome.

J Med Genet 2015 Jun 14;52(6):381-90. Epub 2015 Apr 14.

Department of Cell & Systems Biology, University of Toronto, Toronto, Ontario, Canada Centre for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1136/jmedgenet-2014-102707DOI Listing
June 2015

Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencing.

Am J Med Genet A 2015 Jun 21;167(6):1337-41. Epub 2015 Apr 21.

Division of Otolaryngology, Head and Neck Surgery, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.

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http://dx.doi.org/10.1002/ajmg.a.36969DOI Listing
June 2015

Whole-exome sequencing as a diagnostic tool: current challenges and future opportunities.

Expert Rev Mol Diagn 2015 Jun 9;15(6):749-60. Epub 2015 May 9.

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

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http://www.ambrygen.com/sites/default/files/web/publications
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http://dx.doi.org/10.1586/14737159.2015.1039516DOI Listing
June 2015

Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.

Am J Hum Genet 2015 Jun 28;96(6):971-8. Epub 2015 May 28.

Department of Physiological Sciences, Oklahoma State University, Stillwater, OK 74078, USA; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73126, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.04.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457947PMC
June 2015

Assays of fibrin network properties altered by VKAs in atrial fibrillation - importance of using an appropriate coagulation trigger.

Thromb Haemost 2015 Apr 18;113(4):851-61. Epub 2014 Dec 18.

Shu He, MD, PhD, Building 8-9, 6th floor, Danderyds Hospital, 182 88 Stockholm, Sweden, Tel.: 46+762115129, Fax: 46+812356187, E-mail:

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http://dx.doi.org/10.1160/TH14-07-0591DOI Listing
April 2015

A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature.

BMC Med Genet 2015 Apr 30;16:28. Epub 2015 Apr 30.

Department of Pediatrics and Child Health, University of Manitoba, FE229 Community Services Bldg, 685 William Ave, Winnipeg, MB, R3E 0Z2, Canada.

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http://dx.doi.org/10.1186/s12881-015-0175-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630843PMC
April 2015

Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.

Cell Rep 2015 Mar 5;10(9):1585-1598. Epub 2015 Mar 5.

Division of Molecular Neurobiology, National Institute for Basic Biology, Okazaki 444-8787, Japan; School of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Okazaki 444-8787, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2015.02.011DOI Listing
March 2015

THEMIS is required for pathogenesis of cerebral malaria and protection against pulmonary tuberculosis.

Infect Immun 2015 Feb 1;83(2):759-68. Epub 2014 Dec 1.

Department of Human Genetics, McGill University, Montreal, QC, Canada Complex Traits Group, McGill University, Montreal, QC, Canada Department of Biochemistry, McGill University, Montreal, QC, Canada

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http://dx.doi.org/10.1128/IAI.02586-14DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294254PMC
February 2015

Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype.

Cancer Discov 2015 Feb 3;5(2):135-42. Epub 2014 Dec 3.

Department of Cancer Biology, Abramson Family Cancer Research Institute, Basser Research Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. Department of Pathology, Abramson Family Cancer Research Institute, Basser Research Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1158/2159-8290.CD-14-1156DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320660PMC
February 2015

CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation.

J Exp Med 2014 Dec 17;211(13):2519-35. Epub 2014 Nov 17.

Department of Biochemistry, Department of Human Genetics, McGill and Genome Quebec Innovation Center, Complex Traits Group, McGill University, Montreal, Quebec H3A 0G4, Canada Department of Biochemistry, Department of Human Genetics, McGill and Genome Quebec Innovation Center, Complex Traits Group, McGill University, Montreal, Quebec H3A 0G4, Canada Department of Biochemistry, Department of Human Genetics, McGill and Genome Quebec Innovation Center, Complex Traits Group, McGill University, Montreal, Quebec H3A 0G4, Canada

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http://dx.doi.org/10.1084/jem.20140455DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267237PMC
December 2014