Search

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 numberTitle of the applicationFiling DateStatus
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
Menu