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1
BNT162b2 Vaccine Booster and Mortality Due to Covid-19
BNT162b2 Vaccine Booster and Mortality Due to Covid-19
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BNT162b2 Vaccine Booster and Mortality Due to Covid-19

New England Journal of Medicine, 2021-12, Vol.385 (26), p.2413-2420 [Peer Reviewed Journal]

Copyright © 2021 Massachusetts Medical Society. All rights reserved. ;Copyright © 2021 Massachusetts Medical Society. ;COPYRIGHT 2021 Massachusetts Medical Society ;2021. Not withstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.nejm.org/about-nejm/permissions?query=footer ;Copyright © 2021 Massachusetts Medical Society. All rights reserved. 2021 Massachusetts Medical Society ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa2115624 ;PMID: 34879190

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2
Protection against Covid-19 by BNT162b2 Booster across Age Groups
Protection against Covid-19 by BNT162b2 Booster across Age Groups
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Protection against Covid-19 by BNT162b2 Booster across Age Groups

New England Journal of Medicine, 2021-12, Vol.385 (26), p.2421-2430 [Peer Reviewed Journal]

Copyright © 2021 Massachusetts Medical Society. All rights reserved. ;Copyright © 2021 Massachusetts Medical Society. ;COPYRIGHT 2021 Massachusetts Medical Society ;2021. Not withstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.nejm.org/about-nejm/permissions?query=footer ;Copyright © 2021 Massachusetts Medical Society. All rights reserved. 2021 Massachusetts Medical Society ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa2115926 ;PMID: 34879188

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3
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy
Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy
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Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

The Journal of clinical investigation, 2021-03, Vol.131 (5), p.1-12 [Peer Reviewed Journal]

COPYRIGHT 2021 American Society for Clinical Investigation ;COPYRIGHT 2021 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Mar 2021 ;2021 American Society for Clinical Investigation 2021 American Society for Clinical Investigation ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/jci142148 ;PMID: 33645542

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4
Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis
Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis
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Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis

American journal of human genetics, 2012-12, Vol.91 (6), p.1065-1072 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2014 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Dec 7, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.09.015 ;PMID: 23176824 ;CODEN: AJHGAG

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5
Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children
Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children
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Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children

Annals of the rheumatic diseases, 2014-04, Vol.73 (4), p.662-667 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2014 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0003-4967 ;EISSN: 1468-2060 ;DOI: 10.1136/annrheumdis-2012-202708 ;PMID: 23463692 ;CODEN: ARDIAO

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6
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
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A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci

PLoS genetics, 2012-03, Vol.8 (3), p.e1002559-e1002559 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Kenny et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Kenny EE, Pe'er I, Karban A, Ozelius L, Mitchell AA, et al. (2012) A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci. PLoS Genet 8(3): e1002559. doi:10.1371/journal.pgen.1002559 ;Kenny et al. 2012 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002559 ;PMID: 22412388

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7
Comprehensive overview of the pharmacogenetic diversity in Ashkenazi Jews
Comprehensive overview of the pharmacogenetic diversity in Ashkenazi Jews
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Comprehensive overview of the pharmacogenetic diversity in Ashkenazi Jews

Journal of medical genetics, 2018-09, Vol.55 (9), p.617-627 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ. ;2018 Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2018-105429 ;PMID: 29970487

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8
Hereditary sensory autonomic neuropathy caused by a mutation in dystonin
Hereditary sensory autonomic neuropathy caused by a mutation in dystonin
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Hereditary sensory autonomic neuropathy caused by a mutation in dystonin

Annals of neurology, 2012-04, Vol.71 (4), p.569-572 [Peer Reviewed Journal]

Copyright © 2012 American Neurological Association ;2015 INIST-CNRS ;Copyright © 2012 American Neurological Association. ;ISSN: 0364-5134 ;EISSN: 1531-8249 ;DOI: 10.1002/ana.23524 ;PMID: 22522446 ;CODEN: ANNED3

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9
Promoting Reconciliation Through the Satisfaction of the Emotional Needs of Victimized and Perpetrating Group Members: The Needs-Based Model of Reconciliation
Promoting Reconciliation Through the Satisfaction of the Emotional Needs of Victimized and Perpetrating Group Members: The Needs-Based Model of Reconciliation
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Promoting Reconciliation Through the Satisfaction of the Emotional Needs of Victimized and Perpetrating Group Members: The Needs-Based Model of Reconciliation

Personality & social psychology bulletin, 2009-08, Vol.35 (8), p.1021-1030 [Peer Reviewed Journal]

Copyright SAGE PUBLICATIONS, INC. Aug 2009 ;ISSN: 0146-1672 ;EISSN: 1552-7433 ;DOI: 10.1177/0146167209336610 ;PMID: 19498070

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10
Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene
Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene
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Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene

PLoS genetics, 2016-05, Vol.12 (5), p.e1006008-e1006008 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Gene. PLoS Genet 12(5): e1006008. doi:10.1371/journal.pgen.1006008 ;2016 Vodo et al 2016 Vodo et al ;2016 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Gene. PLoS Genet 12(5): e1006008. doi:10.1371/journal.pgen.1006008 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1006008 ;PMID: 27148741

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11
Relative contributions of BRCA1 and BRCA2 mutations to “triple-negative” breast cancer in Ashkenazi Women
Relative contributions of BRCA1 and BRCA2 mutations to “triple-negative” breast cancer in Ashkenazi Women
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Relative contributions of BRCA1 and BRCA2 mutations to “triple-negative” breast cancer in Ashkenazi Women

Breast cancer research and treatment, 2011-08, Vol.129 (1), p.185-190 [Peer Reviewed Journal]

Springer Science+Business Media, LLC. 2011 ;2015 INIST-CNRS ;Springer Science+Business Media, LLC. 2011 2011 ;ISSN: 0167-6806 ;EISSN: 1573-7217 ;DOI: 10.1007/s10549-011-1433-2 ;PMID: 21394499 ;CODEN: BCTRD6

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12
When the Past is Far from Dead: How Ongoing Consequences of Genocides Committed by the Ingroup Impact Collective Guilt
When the Past is Far from Dead: How Ongoing Consequences of Genocides Committed by the Ingroup Impact Collective Guilt
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When the Past is Far from Dead: How Ongoing Consequences of Genocides Committed by the Ingroup Impact Collective Guilt

Journal of social issues, 2013-03, Vol.69 (1), p.74-91 [Peer Reviewed Journal]

2013 The Society for the Psychological Study of Social Issues ;Copyright Blackwell Publishing Ltd. 2013 ;ISSN: 0022-4537 ;EISSN: 1540-4560 ;DOI: 10.1111/josi.12004 ;CODEN: JSISAF

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13
Connecting Existing Cemeteries Saving Good Soils (for Livings)
Connecting Existing Cemeteries Saving Good Soils (for Livings)
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Connecting Existing Cemeteries Saving Good Soils (for Livings)

Sustainability, 2020-01, Vol.12 (1), p.93 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2071-1050 ;EISSN: 2071-1050 ;DOI: 10.3390/su12010093

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14
The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event
The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event
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The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event

American journal of human genetics, 2006-03, Vol.78 (3), p.487-497 [Peer Reviewed Journal]

2006 The American Society of Human Genetics ;Copyright University of Chicago, acting through its Press Mar 2006 ;2006 by The American Society of Human Genetics. All rights reserved. 2006 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/500307 ;PMID: 16404693

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15
Threat, Dehumanization, and Support for Retaliatory Aggressive Policies in Asymmetric Conflict
Threat, Dehumanization, and Support for Retaliatory Aggressive Policies in Asymmetric Conflict
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Threat, Dehumanization, and Support for Retaliatory Aggressive Policies in Asymmetric Conflict

The Journal of conflict resolution, 2008-02, Vol.52 (1), p.93-116 [Peer Reviewed Journal]

Copyright 2008 Sage Publications ;Copyright SAGE PUBLICATIONS, INC. Feb 2008 ;ISSN: 0022-0027 ;EISSN: 1552-8766 ;DOI: 10.1177/0022002707308597 ;CODEN: JCFRAL

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16
Diasporas and International Relations Theory
Diasporas and International Relations Theory
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Diasporas and International Relations Theory

International organization, 2003-07, Vol.57 (3), p.449-479 [Peer Reviewed Journal]

Copyright © The IO Foundation 2003 ;Copyright 2003 The IO Foundation ;ISSN: 0020-8183 ;EISSN: 1531-5088 ;DOI: 10.1017/S0020818303573015 ;CODEN: IOCMFZ

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17
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy
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Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

Journal of medical genetics, 2007-05, Vol.44 (5), p.322-326 [Peer Reviewed Journal]

Copyright 2007 Journal of Medical Genetics ;2007 INIST-CNRS ;Copyright: 2007 Copyright 2007 Journal of Medical Genetics ;Copyright © 2007 BMJ Publishing Group Ltd ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.2006.046904 ;PMID: 17220209 ;CODEN: JMDGAE

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18
IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein
IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein
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IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein

PloS one, 2009-03, Vol.4 (3), p.e4719-e4719 [Peer Reviewed Journal]

COPYRIGHT 2009 Public Library of Science ;2009 Michelsen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Michelsen et al. 2009 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0004719 ;PMID: 19262684

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19
Is My Home My Castle? Place Attachment, Risk Perception, and Religious Faith
Is My Home My Castle? Place Attachment, Risk Perception, and Religious Faith
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Is My Home My Castle? Place Attachment, Risk Perception, and Religious Faith

Environment and behavior, 2006-03, Vol.38 (2), p.248-265 [Peer Reviewed Journal]

Copyright SAGE PUBLICATIONS, INC. Mar 2006 ;ISSN: 0013-9165 ;EISSN: 1552-390X ;DOI: 10.1177/0013916505277608 ;CODEN: EVBHAF

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20
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population
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Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population

European journal of human genetics : EJHG, 2001-07, Vol.9 (7), p.553-555 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2001 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5200674 ;PMID: 11464248

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