
Edward Raymond
Examiner (ID: 11182, Phone: (571)272-2221 , Office: P/2857 )
| Most Active Art Unit | 2857 |
| Art Unit(s) | 2857 |
| Total Applications | 1533 |
| Issued Applications | 1393 |
| Pending Applications | 52 |
| Abandoned Applications | 93 |
Applications
| Application number | Title of the application | Filing Date | Status |
|---|---|---|---|
Array
(
[id] => 6161213
[patent_doc_number] => 20110159494
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-06-30
[patent_title] => 'Analyzing the FMR1 Gene'
[patent_app_type] => utility
[patent_app_number] => 13/043199
[patent_app_country] => US
[patent_app_date] => 2011-03-08
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 19
[patent_figures_cnt] => 19
[patent_no_of_words] => 34939
[patent_no_of_claims] => 15
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0159/20110159494.pdf
[firstpage_image] =>[orig_patent_app_number] => 13043199
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/043199 | Analyzing the FMR1 Gene | Mar 7, 2011 | Abandoned |
Array
(
[id] => 7663265
[patent_doc_number] => 20110312534
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-12-22
[patent_title] => 'METHOD FOR PREDICTION OF HUMAN IRIS COLOR'
[patent_app_type] => utility
[patent_app_number] => 13/041109
[patent_app_country] => US
[patent_app_date] => 2011-03-04
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 11
[patent_figures_cnt] => 11
[patent_no_of_words] => 27647
[patent_no_of_claims] => 24
[patent_no_of_ind_claims] => 7
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0312/20110312534.pdf
[firstpage_image] =>[orig_patent_app_number] => 13041109
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/041109 | METHOD FOR PREDICTION OF HUMAN IRIS COLOR | Mar 3, 2011 | Abandoned |
Array
(
[id] => 7567367
[patent_doc_number] => 20110287430
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-11-24
[patent_title] => 'NON-THIOPURINE METHYLTRANSFERASE RELATED EFFECTS IN 6-MERCAPTOPURINE THERAPY'
[patent_app_type] => utility
[patent_app_number] => 13/039505
[patent_app_country] => US
[patent_app_date] => 2011-03-03
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 2
[patent_figures_cnt] => 2
[patent_no_of_words] => 8675
[patent_no_of_claims] => 24
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0287/20110287430.pdf
[firstpage_image] =>[orig_patent_app_number] => 13039505
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/039505 | Non-thiopurine methyltransferase related effects in 6-mercaptopurine therapy | Mar 2, 2011 | Issued |
Array
(
[id] => 8617662
[patent_doc_number] => 20130022975
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-01-24
[patent_title] => 'METHOD FOR DETECTING ARTERIOSCLEROTIC DISEASES ON THE BASIS OF SINGLE NUCLEOTIDE POLYMORPHISM AT HUMAN CHROMOSOME 5P15.3'
[patent_app_type] => utility
[patent_app_number] => 13/579463
[patent_app_country] => US
[patent_app_date] => 2011-02-18
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 1
[patent_figures_cnt] => 1
[patent_no_of_words] => 5231
[patent_no_of_claims] => 6
[patent_no_of_ind_claims] => 3
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13579463
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/579463 | METHOD FOR DETECTING ARTERIOSCLEROTIC DISEASES ON THE BASIS OF SINGLE NUCLEOTIDE POLYMORPHISM AT HUMAN CHROMOSOME 5P15.3 | Feb 17, 2011 | Abandoned |
Array
(
[id] => 11794403
[patent_doc_number] => 09404158
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2016-08-02
[patent_title] => 'Alternative splicing variant of OATP1B3 mRNA'
[patent_app_type] => utility
[patent_app_number] => 13/030485
[patent_app_country] => US
[patent_app_date] => 2011-02-18
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 8
[patent_figures_cnt] => 10
[patent_no_of_words] => 17304
[patent_no_of_claims] => 3
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 14
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13030485
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/030485 | Alternative splicing variant of OATP1B3 mRNA | Feb 17, 2011 | Issued |
Array
(
[id] => 9112815
[patent_doc_number] => 08568984
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2013-10-29
[patent_title] => 'Methods of diagnosing non-urinary tract diseases by detecting aberrant methylation'
[patent_app_type] => utility
[patent_app_number] => 13/030888
[patent_app_country] => US
[patent_app_date] => 2011-02-18
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 7
[patent_figures_cnt] => 16
[patent_no_of_words] => 15135
[patent_no_of_claims] => 1
[patent_no_of_ind_claims] => 1
[patent_words_short_claim] => 141
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13030888
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/030888 | Methods of diagnosing non-urinary tract diseases by detecting aberrant methylation | Feb 17, 2011 | Issued |
Array
(
[id] => 8814550
[patent_doc_number] => 20130115595
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-05-09
[patent_title] => 'METHOD TO DETECT REPEAT SEQUENCE MOTIFS IN NUCLEIC ACID'
[patent_app_type] => utility
[patent_app_number] => 13/576740
[patent_app_country] => US
[patent_app_date] => 2011-02-04
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 25
[patent_figures_cnt] => 25
[patent_no_of_words] => 23309
[patent_no_of_claims] => 45
[patent_no_of_ind_claims] => 4
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13576740
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/576740 | Method to detect repeat sequence motifs in nucleic acid | Feb 3, 2011 | Issued |
Array
(
[id] => 5936676
[patent_doc_number] => 20110212460
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-09-01
[patent_title] => 'ASSAY FOR NITROUS OXIDE NEUROLOGIC SYNDROME'
[patent_app_type] => utility
[patent_app_number] => 13/012561
[patent_app_country] => US
[patent_app_date] => 2011-01-24
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 4
[patent_figures_cnt] => 4
[patent_no_of_words] => 5713
[patent_no_of_claims] => 31
[patent_no_of_ind_claims] => 5
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0212/20110212460.pdf
[firstpage_image] =>[orig_patent_app_number] => 13012561
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/012561 | ASSAY FOR NITROUS OXIDE NEUROLOGIC SYNDROME | Jan 23, 2011 | Abandoned |
Array
(
[id] => 6177201
[patent_doc_number] => 20110177958
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-07-21
[patent_title] => 'METHODS AND MATERIALS FOR IDENTIFYING POLYMORPHIC VARIANTS, DIAGNOSING SUSCEPTIBILITIES, AND TREATING DISEASE'
[patent_app_type] => utility
[patent_app_number] => 13/008528
[patent_app_country] => US
[patent_app_date] => 2011-01-18
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 42543
[patent_no_of_claims] => 18
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0177/20110177958.pdf
[firstpage_image] =>[orig_patent_app_number] => 13008528
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/008528 | METHODS AND MATERIALS FOR IDENTIFYING POLYMORPHIC VARIANTS, DIAGNOSING SUSCEPTIBILITIES, AND TREATING DISEASE | Jan 17, 2011 | Abandoned |
Array
(
[id] => 8042171
[patent_doc_number] => 20120070826
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-03-22
[patent_title] => 'LAFORA\'S DISEASE GENE'
[patent_app_type] => utility
[patent_app_number] => 13/007469
[patent_app_country] => US
[patent_app_date] => 2011-01-14
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 15
[patent_figures_cnt] => 15
[patent_no_of_words] => 20153
[patent_no_of_claims] => 16
[patent_no_of_ind_claims] => 4
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0070/20120070826.pdf
[firstpage_image] =>[orig_patent_app_number] => 13007469
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/007469 | Lafora's disease gene | Jan 13, 2011 | Issued |
Array
(
[id] => 8453181
[patent_doc_number] => 20120264127
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-10-18
[patent_title] => 'SIMULTANEOUS DETECTION OF MUTATIONAL STATUS AND GENE COPY NUMBER'
[patent_app_type] => utility
[patent_app_number] => 13/518135
[patent_app_country] => US
[patent_app_date] => 2010-12-30
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 16
[patent_figures_cnt] => 16
[patent_no_of_words] => 14257
[patent_no_of_claims] => 19
[patent_no_of_ind_claims] => 3
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13518135
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/518135 | SIMULTANEOUS DETECTION OF MUTATIONAL STATUS AND GENE COPY NUMBER | Dec 29, 2010 | Abandoned |
Array
(
[id] => 10070905
[patent_doc_number] => 09109253
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2015-08-18
[patent_title] => 'Oligonucleotides and methods for detecting lavender foal syndrome'
[patent_app_type] => utility
[patent_app_number] => 13/512536
[patent_app_country] => US
[patent_app_date] => 2010-12-01
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 1
[patent_figures_cnt] => 1
[patent_no_of_words] => 4326
[patent_no_of_claims] => 6
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 85
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13512536
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/512536 | Oligonucleotides and methods for detecting lavender foal syndrome | Nov 30, 2010 | Issued |
Array
(
[id] => 8198053
[patent_doc_number] => 20120122087
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-05-17
[patent_title] => '5-Hydroxymethylcytosine as a biomarker for early detection, treatment and prognostic monitoring of cancer'
[patent_app_type] => utility
[patent_app_number] => 12/927512
[patent_app_country] => US
[patent_app_date] => 2010-11-17
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 5
[patent_figures_cnt] => 5
[patent_no_of_words] => 3896
[patent_no_of_claims] => 10
[patent_no_of_ind_claims] => 1
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0122/20120122087.pdf
[firstpage_image] =>[orig_patent_app_number] => 12927512
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/927512 | 5-Hydroxymethylcytosine as a biomarker for early detection, treatment and prognostic monitoring of cancer | Nov 16, 2010 | Abandoned |
Array
(
[id] => 7487385
[patent_doc_number] => 20110236370
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-09-29
[patent_title] => 'Genetic Alterations on Chromosomes 21q, 6q and 15q and Methods of Use Thereof for the Diagnosis and Treatment of Type I Diabetes'
[patent_app_type] => utility
[patent_app_number] => 12/947564
[patent_app_country] => US
[patent_app_date] => 2010-11-16
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 3
[patent_figures_cnt] => 3
[patent_no_of_words] => 21541
[patent_no_of_claims] => 26
[patent_no_of_ind_claims] => 9
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0236/20110236370.pdf
[firstpage_image] =>[orig_patent_app_number] => 12947564
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/947564 | Genetic Alterations on Chromosomes 21q, 6q and 15q and Methods of Use Thereof for the Diagnosis and Treatment of Type I Diabetes | Nov 15, 2010 | Abandoned |
Array
(
[id] => 6055049
[patent_doc_number] => 20110111409
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-05-12
[patent_title] => 'METHODS FOR DEPLETING RNA FROM NUCLEIC ACID SAMPLES'
[patent_app_type] => utility
[patent_app_number] => 12/940981
[patent_app_country] => US
[patent_app_date] => 2010-11-05
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 15
[patent_figures_cnt] => 15
[patent_no_of_words] => 13943
[patent_no_of_claims] => 49
[patent_no_of_ind_claims] => 32
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0111/20110111409.pdf
[firstpage_image] =>[orig_patent_app_number] => 12940981
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/940981 | Methods for depleting RNA from nucleic acid samples | Nov 4, 2010 | Issued |
Array
(
[id] => 6161196
[patent_doc_number] => 20110159491
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-06-30
[patent_title] => 'Method for detecting cytosine methylation in DNA samples'
[patent_app_type] => utility
[patent_app_number] => 12/925843
[patent_app_country] => US
[patent_app_date] => 2010-10-29
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 1
[patent_figures_cnt] => 1
[patent_no_of_words] => 4842
[patent_no_of_claims] => 26
[patent_no_of_ind_claims] => 1
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0159/20110159491.pdf
[firstpage_image] =>[orig_patent_app_number] => 12925843
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/925843 | Method for detecting cytosine methylation in DNA samples | Oct 28, 2010 | Abandoned |
Array
(
[id] => 7567355
[patent_doc_number] => 20110287418
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-11-24
[patent_title] => 'Compositions and Methods for Diagnosis and Treatment of Epilepsy'
[patent_app_type] => utility
[patent_app_number] => 12/914844
[patent_app_country] => US
[patent_app_date] => 2010-10-28
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 27
[patent_figures_cnt] => 27
[patent_no_of_words] => 42215
[patent_no_of_claims] => 28
[patent_no_of_ind_claims] => 3
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0287/20110287418.pdf
[firstpage_image] =>[orig_patent_app_number] => 12914844
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/914844 | Compositions and methods for diagnosis and treatment of epilepsy | Oct 27, 2010 | Issued |
Array
(
[id] => 8523269
[patent_doc_number] => 20120322677
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-12-20
[patent_title] => 'PREDICTING BENEFIT OF ANTI-CANCER THERAPY VIA ARRAY COMPARATIVE GENOMIC HYBRIDIZATION'
[patent_app_type] => utility
[patent_app_number] => 13/502696
[patent_app_country] => US
[patent_app_date] => 2010-10-19
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 18
[patent_figures_cnt] => 18
[patent_no_of_words] => 23266
[patent_no_of_claims] => 29
[patent_no_of_ind_claims] => 9
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13502696
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/502696 | PREDICTING BENEFIT OF ANTI-CANCER THERAPY VIA ARRAY COMPARATIVE GENOMIC HYBRIDIZATION | Oct 18, 2010 | Abandoned |
Array
(
[id] => 4514439
[patent_doc_number] => 07932042
[patent_country] => US
[patent_kind] => B1
[patent_issue_date] => 2011-04-26
[patent_title] => 'Methods and compositions for the treatment of psychotic disorders through the identification of the olanzapine poor response predictor genetic signature'
[patent_app_type] => utility
[patent_app_number] => 12/903891
[patent_app_country] => US
[patent_app_date] => 2010-10-13
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 1
[patent_figures_cnt] => 1
[patent_no_of_words] => 24419
[patent_no_of_claims] => 6
[patent_no_of_ind_claims] => 2
[patent_words_short_claim] => 85
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] => patents/07/932/07932042.pdf
[firstpage_image] =>[orig_patent_app_number] => 12903891
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/903891 | Methods and compositions for the treatment of psychotic disorders through the identification of the olanzapine poor response predictor genetic signature | Oct 12, 2010 | Issued |
Array
(
[id] => 6001646
[patent_doc_number] => 20110117552
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2011-05-19
[patent_title] => 'METHODS OF USING A NOD2/CARD15 HAPLOTYPE TO DIAGNOSE CROHN\'S DISEASE'
[patent_app_type] => utility
[patent_app_number] => 12/902111
[patent_app_country] => US
[patent_app_date] => 2010-10-11
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 16
[patent_figures_cnt] => 16
[patent_no_of_words] => 16871
[patent_no_of_claims] => 7
[patent_no_of_ind_claims] => 7
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0117/20110117552.pdf
[firstpage_image] =>[orig_patent_app_number] => 12902111
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/902111 | METHODS OF USING A NOD2/CARD15 HAPLOTYPE TO DIAGNOSE CROHN'S DISEASE | Oct 10, 2010 | Abandoned |