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Extract from the Register of European Patents

EP About this file: EP2823055

EP2823055 - A GENOTYPING TEST FOR ASSESSING RISK OF AUTISM [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  08.06.2018
Database last updated on 15.11.2024
FormerGrant of patent is intended
Status updated on  03.09.2017
FormerExamination is in progress
Status updated on  09.08.2017
FormerGrant of patent is intended
Status updated on  23.03.2017
Most recent event   Tooltip08.06.2018Application deemed to be withdrawnpublished on 11.07.2018  [2018/28]
Applicant(s)For all designated states
Integragen
Génopole Campus 1
5, rue Henri Desbruères
Génavenir 8
91000 Evry / FR
[2015/03]
Inventor(s)01 / CARAYOL, Jérôme
103 avenue Henri Ginoux
92120 Montrouge / FR
 [2015/03]
Representative(s)Regimbeau
20, rue de Chazelles
75847 Paris Cedex 17 / FR
[2015/03]
Application number, filing date13708796.108.03.2013
WO2013EP54757
Priority number, dateEP2012030528509.03.2012         Original published format: EP 12305285
US201261608717P09.03.2012         Original published format: US 201261608717 P
[2015/03]
Filing languageEN
Procedural languageEN
PublicationType: A2 Application without search report
No.:WO2013132074
Date:12.09.2013
Language:EN
[2013/37]
Type: A2 Application without search report 
No.:EP2823055
Date:14.01.2015
Language:EN
The application published by WIPO in one of the EPO official languages on 12.09.2013 takes the place of the publication of the European patent application.
[2015/03]
Search report(s)International search report - published on:EP24.10.2013
ClassificationIPC:C12Q1/68
[2015/03]
CPC:
C12Q1/6883 (EP,US); C12Q2600/156 (EP,US); C12Q2600/172 (EP,US)
Designated contracting statesAL,   AT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MK,   MT,   NL,   NO,   PL,   PT,   RO,   RS,   SE,   SI,   SK,   SM,   TR [2015/03]
TitleGerman:GENOTYPISIERUNGSTEST ZUR BEWERTUNG EINES AUTISMUSRISIKOS[2015/03]
English:A GENOTYPING TEST FOR ASSESSING RISK OF AUTISM[2015/03]
French:TEST DE GÉNOTYPAGE POUR ÉVALUER LE RISQUE D'AUTISME[2015/03]
Entry into regional phase09.10.2014National basic fee paid 
09.10.2014Designation fee(s) paid 
09.10.2014Examination fee paid 
Examination procedure09.10.2014Examination requested  [2015/03]
06.05.2015Amendment by applicant (claims and/or description)
20.11.2015Despatch of a communication from the examining division (Time limit: M06)
26.05.2016Reply to a communication from the examining division
24.03.2017Communication of intention to grant the patent
31.07.2017Disapproval of the communication of intention to grant the patent by the applicant or resumption of examination proceedings by the EPO
04.09.2017Communication of intention to grant the patent
16.01.2018Application deemed to be withdrawn, date of legal effect  [2018/28]
20.02.2018Despatch of communication that the application is deemed to be withdrawn, reason: fee for grant / fee for printing not paid in time  [2018/28]
Divisional application(s)The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued is  20.11.2015
Fees paidRenewal fee
10.03.2015Renewal fee patent year 03
08.03.2016Renewal fee patent year 04
08.03.2017Renewal fee patent year 05
Penalty fee
Additional fee for renewal fee
31.03.201806   M06   Not yet paid
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Patent Court		 See the Register of the Unified Patent Court for opt-out data
Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Cited inInternational search[AD]WO2011031786  (LAB CORP AMERICA HOLDINGS [US], et al) [AD] 1-31 * the whole document *;
 [AD]WO2009043178  (HOSPITAL FOR SICK CHILDREN [CA], et al) [AD] 1-31 * paragraph [0012] - paragraph [0014] *;
 [AD]US2011207124  (HAKONARSON HAKON [US], et al) [AD] 1-31 * paragraph [0011] - paragraph [0013] * * paragraph [0026] - paragraph [0027] * * paragraph [0063] - paragraph [0066] * * example 1; tables 1, 8-14 *;
 [YDA]WO2011138372  (INTEGRAGEN SA [FR], et al) [YD] 9,14,19 * the whole document * [A] 1-8,10-13,15-18,20-31;
 [AD]US2011086777  (CARAYOL JEROME [FR], et al) [AD] 1-31 * paragraph [0013]; claims 1-20 *;
    [IDAY] - HUSSMAN JOHN P ET AL, "A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism", MOLECULAR AUTISM, BIOMED CENTRAL LTD, LONDON, UK, (20110119), vol. 2, no. 1, doi:10.1186/2040-2392-2-1, ISSN 2040-2392, page 1, XP021091460 [ID] 1-8,10-13,15-18,20-23,31 * abstract * * page 4, column 2, paragraph 2 - page 5, column 1, paragraph 1 * [A] 24-30 [Y] 9,14,19

DOI:   http://dx.doi.org/10.1186/2040-2392-2-1
 [AD]  - ANA M COUTINHO ET AL, "Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels", HUMAN GENETICS, SPRINGER, BERLIN, DE, (20070103), vol. 121, no. 2, doi:10.1007/S00439-006-0301-3, ISSN 1432-1203, pages 243 - 256, XP019492052 [AD] 1-14,20-31 * abstract * * page 245, column 2, paragraph 3 * * page 247, column 2, paragraph 2 *

DOI:   http://dx.doi.org/10.1007/s00439-006-0301-3
 [AD]  - IRINA VOINEAGU ET AL, "Transcriptomic analysis of autistic brain reveals convergent molecular pathology", NATURE, (20110101), vol. 474, no. 7351, doi:10.1038/nature10110, ISSN 0028-0836, pages 380 - 384, XP055038194 [AD] 1-14,20-31 * abstract * * page 383, column 1, paragraph 3 - page 384, column 1, paragraph 1 *

DOI:   http://dx.doi.org/10.1038/nature10110
 [AD]  - CHRISTA LESE MARTIN ET AL, "Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism", AMERICAN JOURNAL OF MEDICAL GENETICS PART B: NEUROPSYCHIATRIC GENETICS, (20071005), vol. 144B, no. 7, doi:10.1002/ajmg.b.30530, ISSN 1552-4841, pages 869 - 876, XP055038144 [AD] 1-14,20-31 * abstract *

DOI:   http://dx.doi.org/10.1002/ajmg.b.30530
 [AD]  - MORROW ERIC M ET AL, "Identifying autism loci and genes by tracing recent shared ancestry", SCIENCE, AMERICAN ASSOCIATION FOR THE ADVANCEMENT OF SCIENCE, US, (20080711), vol. 321, no. 5886, doi:10.1126/SCIENCE.1157657, ISSN 1095-9203, pages 218 - 223, XP002557034 [AD] 1-31 * abstract * * page 221, column 3, paragraph 2 - page 222, column 1, paragraph 1 * * page 222, column 2, paragraph 2; figure 4 *

DOI:   http://dx.doi.org/10.1126/science.1157657
 [AD]  - KAI WANG ET AL, "Common genetic variants on 5p14.1 associate with autism spectrum disorders", NATURE, (20090528), vol. 459, no. 7246, doi:10.1038/nature07999, ISSN 0028-0836, pages 528 - 533, XP055022181 [AD] 1-31 * abstract * * page 529, column 2, paragraph 2; table 3 *

DOI:   http://dx.doi.org/10.1038/nature07999
 [AD]  - LAUREN A. WEISS ET AL, "A genome-wide linkage and association scan reveals novel loci for autism", NATURE, (20091008), vol. 461, no. 7265, doi:10.1038/nature08490, ISSN 0028-0836, pages 802 - 808, XP055038202 [AD] 1-31 * abstract *

DOI:   http://dx.doi.org/10.1038/nature08490
 [AD]  - R. ANNEY ET AL, "A genome-wide scan for common alleles affecting risk for autism", HUMAN MOLECULAR GENETICS, (20101015), vol. 19, no. 20, doi:10.1093/hmg/ddq307, ISSN 0964-6906, pages 4072 - 4082, XP055038209 [AD] 1-31 * the whole document *

DOI:   http://dx.doi.org/10.1093/hmg/ddq307
 [YDA]  - CARAYOL JEROME ET AL, "Autism risk assessment in siblings of affected children using sex-specific genetic scores.", MOLECULAR AUTISM 2011 LNKD- PUBMED:22017886, (2011), vol. 2, no. 1, ISSN 2040-2392, page 17, XP002683734 [YD] 9,14,19 * abstract * [A] 1-8,10-13,15-18,20-31

DOI:   http://dx.doi.org/10.1186/2040-2392-2-17
 [AD]  - CARAYOL JEROME ET AL, "Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk", MOLECULAR AUTISM, BIOMED CENTRAL LTD, LONDON, UK, (20100222), vol. 1, no. 1, ISSN 2040-2392, page 4, XP021070693 [AD] 1-31 * abstract * * page 2, column 1, paragraph 2 *
 [AD]  - IRINA VOINEAGU, "Gene expression studies in autism: Moving from the genome to the transcriptome and beyond", NEUROBIOLOGY OF DISEASE, (20120101), vol. 45, no. 1, doi:10.1016/j.nbd.2011.07.017, ISSN 0969-9961, pages 69 - 75, XP055038195 [AD] 1-31 * abstract * * page 70, column 1, paragraph 6 - column 2, paragraph 1 *

DOI:   http://dx.doi.org/10.1016/j.nbd.2011.07.017
 [AD]  - ABRAHAMS B S ET AL, "Advances in autism genetics: on the threshold of a new neurobiology", NATURE REVIEWS GENETICS, NATURE PUBLISHING GROUP, GB, vol. 9, no. 5, doi:10.1038/NRG2346, ISSN 1471-0056, (20080501), pages 341 - 355, (20080415), XP002537731 [AD] 1-31 * abstract * * page 349, column 1, paragraph 2 - page 351, column 2, paragraph 1; tables 3, 4 *

DOI:   http://dx.doi.org/10.1038/NRG2346
 [X]  - MICHAEL A EBERLE ET AL, "Power to detect risk alleles using genome-wide tag SNP panels", PLOS GENETICS, PUBLIC LIBRARY OF SCIENCE, SAN FRANCISCO, CA, US, (20071005), vol. 3, no. 10, doi:10.1371/JOURNAL.PGEN.0030170, ISSN 1553-7390, XP002664350 [X] 24-30 * abstract * * page 1828, column 1, paragraph 2 - column 2, paragraph 1 *

DOI:   http://dx.doi.org/10.1371/JOURNAL.PGEN.0030170
 [T]  - GUNDERSON K L ET AL, "A genome-wide scalable SNP genotyping assay using microarray technology", NATURE GENETICS, NATURE PUBLISHING GROUP, NEW YORK, US, (20050417), vol. 37, no. 5, doi:10.1038/NG1547, ISSN 1061-4036, pages 549 - 554, XP002396335 [T] 24-30 * the whole document *

DOI:   http://dx.doi.org/10.1038/ng1547
 [AD]  - STEPHEN W SCHERER ET AL, "Risk factors for autism: translating genomic discoveries into diagnostics", HUMAN GENETICS, SPRINGER, BERLIN, DE, (20110624), vol. 130, no. 1, doi:10.1007/S00439-011-1037-2, ISSN 1432-1203, pages 123 - 148, XP019925155 [AD] 1-31 * abstract *

DOI:   http://dx.doi.org/10.1007/s00439-011-1037-2
 [T]  - LIEBAERT F. ET AL., "Use of common genetic variants to identify risk of autism in siblings of children diagnosed with autism spectrum disorders.", Toronto, Canada, no. 126.002, (20120519), International Meeting for Autism Research. Toronto, Canada, 17-19 May 2012., URL: https://imfar.confex.com/imfar/2012/IMFAR_2012_Program.pdf, (20120918), XP002683735 [T] 1-31 * abstract *
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.