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SECTION VI
List of Publications
Conferences Attended
168
LIST OF PUBLICATIONS
1. Avinash MV, Bhanu Priya R and Ramachandra NB. 2009. Designing a
Biosoftware: Human Phenopaedia and Genome Sequence Analyzer”. Proceedings
of National Conference on “Information Technology and its Applications 153-157.
Centre for Information Science and Technology, University of Mysore.
2. Avinash MV, Prakash P and Ramachandra NB. Copy Number Variation analysis
in humans reveal previously identified X chromosome Transposed Region (XTR)
in Y-chromosome to be a pseudoautosomal region 3 (PAR3). Funct Integr
Genomic DOI: 10.1007/s10142-013-0323-6 (In press). [IF: 2.84]
4. Avinash MV, Marieta S, Prakash P and Ramachandra NB. Family based genome-
wide copy number scan identifies five new genes of dyslexia involved in dendritic
spinal plasticity. J Hum Genet. (In press). [IF: 2.57]
5. Avinash MV, Marieta S, Prakash P and Ramachandra NB. Whole genome scan
identifies PCDH11X as candidate gene for developmental dyslexia (Under
Review).
6. Avinash MV, Marieta S, Prakash P and Ramachandra NB. Family based genome-
wide copy number scan identifies 17q21.31 microdeletion syndrome in dyslexics
(Under Review).
7. Avinash MV, Prakash P and Ramachandra NB. Copy Number Polymorphism of
UGT2B17 in India is not associated with any diseases as revealed by Whole
Genome scan (Under Review).
169
PAPERS PRESENTED IN CONFERENCE
1. Avinash M Veerappa, Anand S, Marita Priya JS, Shyamala KV, Prakash P, and
NB Ramachandra (2010) Genetics of Developmental Dyslexia held during 6th & 9th
March- 2010 presented the paper in the XIX Annual Conference of National
Academy of Psychology (NAOP) Organized by Department of Psychology,
Bangalore University, India.
2. Avinash MV, Marieta S, Prakash P and Ramachandra NB. (2012) Presented a
poster titled “Family based genome-wide copy number scan identifies five new
genes of dyslexia involved in dendritic spinal plasticity” in the Human Genome
Meet organized by the Human Genome Organisation in Sydney, Australia from
11TH to 14TH March 2012.
170
Editorial Manager Registration – Acceptance Letter
Date: 01 Apr 2013 To: "Ramachandra B Nallur" [email protected]
From: "Rudi Appels" [email protected]
Subject: FIGE: Your manuscript entitled Copy Number Variation analysis in humans
reveal previously identified X chromosome Transposed Region (XTR) in Y-chromosome
to be a pseudoautosomal region 3 (PAR3).
Ref.: Ms. No. FIGE-D-12-00106R4
Copy Number Variation analysis in humans reveal previously identified X chromosome
Transposed Region (XTR) in Y-chromosome to be a pseudoautosomal region 3 (PAR3)
Functional & Integrative Genomics
Dear Prof. Nallur,
I am pleased to tell you that your work has now been accepted for publication in
Functional & Integrative Genomics.
Thank you for submitting your work to this journal.
With kind regards
Rudi Appels
Editor-in-Chief
Functional & Integrative Genomics
171
Journal of Human Genetics - Decision on JHG-13-156R
From: [email protected] me, jhgedoc, nallurbr 18th Apr 2013
Dear Prof Ramachandra
It is a pleasure to accept your manuscript entitled "Family based genome-wide copynumber scan identifies five new genes of dyslexia involved in dendritic spinal plasticity" inits current form for publication in Journal of Human Genetics.We will send your manuscript to the publisher for publication once we have received yourLicense to Publish form.
Using the link below please download, print, sign on behalf of all authors, with theirconsent, the License to Publish Form. Please send this form as soon as possible to theeditorial office:
JOURNAL OF HUMAN GENETICS Editorial OfficeDepartment of Human Genetics, Graduate School of MedicineThe University of Tokyo7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 JapanFax: +81-3-5802-8619Email: [email protected]
http://www.nature.com/licenceforms/jhg/jhg-ltp.pdf
For your information, Nature Publishing Group can publish the manuscript with the LTPsigned by the corresponding author only. It is not necessary for all co-authors to sign onthe LTP form.
If your manuscript includes supplementary information, please make sure that the file is infinal format and ready to be published as is. Publisher will not copyedit, pagemake ortypeset supplementary materials. Supplementary information files that are not appropriatefor publication should be replaced or removed by the author before the paper is sent forproduction. To make those changes please contact Editorial office to give instructionbefore submission of the License to Publish form.
When the typeset proof is ready, the production editor from NPG will contact you byemail. In the meantime, if you have any questions regarding this manuscript please contactus at the editorial office at [email protected] at any time.
Thank you very much again for your contribution.
TADAO ARINAMIAssociate EditorJournal of Human Genetics
171
Journal of Human Genetics - Decision on JHG-13-156R
From: [email protected] me, jhgedoc, nallurbr 18th Apr 2013
Dear Prof Ramachandra
It is a pleasure to accept your manuscript entitled "Family based genome-wide copynumber scan identifies five new genes of dyslexia involved in dendritic spinal plasticity" inits current form for publication in Journal of Human Genetics.We will send your manuscript to the publisher for publication once we have received yourLicense to Publish form.
Using the link below please download, print, sign on behalf of all authors, with theirconsent, the License to Publish Form. Please send this form as soon as possible to theeditorial office:
JOURNAL OF HUMAN GENETICS Editorial OfficeDepartment of Human Genetics, Graduate School of MedicineThe University of Tokyo7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 JapanFax: +81-3-5802-8619Email: [email protected]
http://www.nature.com/licenceforms/jhg/jhg-ltp.pdf
For your information, Nature Publishing Group can publish the manuscript with the LTPsigned by the corresponding author only. It is not necessary for all co-authors to sign onthe LTP form.
If your manuscript includes supplementary information, please make sure that the file is infinal format and ready to be published as is. Publisher will not copyedit, pagemake ortypeset supplementary materials. Supplementary information files that are not appropriatefor publication should be replaced or removed by the author before the paper is sent forproduction. To make those changes please contact Editorial office to give instructionbefore submission of the License to Publish form.
When the typeset proof is ready, the production editor from NPG will contact you byemail. In the meantime, if you have any questions regarding this manuscript please contactus at the editorial office at [email protected] at any time.
Thank you very much again for your contribution.
TADAO ARINAMIAssociate EditorJournal of Human Genetics
171
Journal of Human Genetics - Decision on JHG-13-156R
From: [email protected] me, jhgedoc, nallurbr 18th Apr 2013
Dear Prof Ramachandra
It is a pleasure to accept your manuscript entitled "Family based genome-wide copynumber scan identifies five new genes of dyslexia involved in dendritic spinal plasticity" inits current form for publication in Journal of Human Genetics.We will send your manuscript to the publisher for publication once we have received yourLicense to Publish form.
Using the link below please download, print, sign on behalf of all authors, with theirconsent, the License to Publish Form. Please send this form as soon as possible to theeditorial office:
JOURNAL OF HUMAN GENETICS Editorial OfficeDepartment of Human Genetics, Graduate School of MedicineThe University of Tokyo7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 JapanFax: +81-3-5802-8619Email: [email protected]
http://www.nature.com/licenceforms/jhg/jhg-ltp.pdf
For your information, Nature Publishing Group can publish the manuscript with the LTPsigned by the corresponding author only. It is not necessary for all co-authors to sign onthe LTP form.
If your manuscript includes supplementary information, please make sure that the file is infinal format and ready to be published as is. Publisher will not copyedit, pagemake ortypeset supplementary materials. Supplementary information files that are not appropriatefor publication should be replaced or removed by the author before the paper is sent forproduction. To make those changes please contact Editorial office to give instructionbefore submission of the License to Publish form.
When the typeset proof is ready, the production editor from NPG will contact you byemail. In the meantime, if you have any questions regarding this manuscript please contactus at the editorial office at [email protected] at any time.
Thank you very much again for your contribution.
TADAO ARINAMIAssociate EditorJournal of Human Genetics
172
Journal of Human Genetics
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