DR. BASSEM BEJJANI, M.D.
Medical Practice at 6 Ave, Spokane, WA
License number
Washington MTS 4427
Category
Medical Practice
Type
Medical Genetics, Ph.D. Medical Genetics
Address
Address
44 W 6Th Ave SUITE 202, Spokane, WA 99204
Phone
(509) 474-6840
Personal information
See more information about BASSEM BEJJANI at radaris.comName
Address
Phone
21415 Panorama Rd, Colbert, WA 99005
2211 E Beaver Lake Dr SE, Sammamish, WA 98075
721 E Wandermere Estates Ln, Spokane, WA 99208
Organization information
See more information about BASSEM BEJJANI at bizstanding.comBassem Bejjani MD
101 W 8 Ave, Spokane, WA 99204
Industry:
Genetic Medicine, Pediatrician
Bassem Abdu Bejjani
Professional information
See more information about BASSEM BEJJANI at trustoria.com
Bassem Bejjani
Bassem Bejjani
Location:
Spokane, Washington Area
Industry:
Biotechnology
Skills:
Genetics, Molecular Biology, Genomics, Molecular Diagnostics, Biotechnology, Lifesciences, Hardware Diagnostics, Infectious Diseases, Laboratory, Cytogenetics, PCR, Oncology, Cancer, Personalized Medicine, Clinical Research, Molecular Genetics, Hospitals, Healthcare, Medical Devices, Commercialization, Medical Education, Medicine, Public Health, Human Genetics, Pediatrics, Epidemiology, Medical Genetics, Immunology, Biochemistry, Clinical Trials, Cell Biology, Neuroscience, Informatics
Bassem Abdu Bejjani, Spokane WA
Bassem Abdu Bejjani, Spokane WA
Specialties:
Medical Genetics, Clinical Genetics, M.D., Clinical Cytogenetic, Clinical Molecular Genetics, Pediatrics
Work:
Sacred Heart Medical Center
101 W 8Th Ave, Spokane, WA 99204
101 W 8Th Ave, Spokane, WA 99204
Education:
American University Of Beirut (1987)
Dr. Bassem Bejjani - MD (Doctor of Medicine)
Dr. Bassem Bejjani - MD (Doctor of Medicine)
Hospitals:
44 W 6Th Ave SUITE 202, Spokane 99204
21415 N Panorama Rd, Colbert 99005
44 W 6Th Ave SUITE 202, Spokane 99204
21415 N Panorama Rd, Colbert 99005
21415 N Panorama Rd, Colbert 99005
44 W 6Th Ave SUITE 202, Spokane 99204
21415 N Panorama Rd, Colbert 99005
Education:
Medical Schools
American University of Beirut / Faculty of Medicine
American University of Beirut / Faculty of Medicine
Multiplex (+/-) Stranded Arrays And Assays For Detecting Chromosomal Abnormalities Associated With Cancer And Other Diseases
Multiplex (+/-) Stranded Arrays And Assays For Detecting Chromosomal Abnormalities Associated With Cancer And Other Diseases
US Patent:
2011008, Apr 14, 2011
Filed:
Sep 27, 2010
Appl. No.:
12/891623
Inventors:
Lisa McDaniel - Spokane WA, US
Blake Ballif - Greenacres WA, US
Roger Schultz - Spokane WA, US
Brice Tebbs - Spokane WA, US
Bassem Bejjani - Spokane WA, US
Lisa Shaffer - Colbert WA, US
Blake Ballif - Greenacres WA, US
Roger Schultz - Spokane WA, US
Brice Tebbs - Spokane WA, US
Bassem Bejjani - Spokane WA, US
Lisa Shaffer - Colbert WA, US
Assignee:
Signature Genomics Laboratories LLC - Spokane WA
International Classification:
C40B 30/04, C40B 40/08
US Classification:
506 9, 506 17
Abstract:
Multiplex (+/−) stranded analyses, such as array comparative genomic hybridization (aCGH), are provided for detecting chromosomal rearrangements associated with cancer and other diseases. For example, an illustrative multiplex array for CGH includes discrete plus (+) strand and minus (−) strand DNA probes, complementary to each other but separable on the CGH array. The minus (−) strand DNA probes recover diagnostic information lost to conventional microarrays, since many genes transcribe from the minus (−) strand. In an illustrative system, patient and control DNA samples are prepared for CGH by amplification and labeling using comprehensive primers that generate both plus (+) strands and minus (−) strands of DNA in the samples. The breakpoints of a translocated chromosome may be detected on a multiplex microarray by DNA probes of one polarity, while DNA copy number changes associated with the translocation region may be detected by corresponding DNA probes of the complementary polarity. Related methods for identifying translocation partner genes are also provided.
Web-Based Genetics Analysis
Web-Based Genetics Analysis
US Patent:
2010011, May 6, 2010
Filed:
Nov 5, 2008
Appl. No.:
12/265396
Inventors:
Bassem A. Bejjani - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Blake Ballif - Greenacres WA, US
Brice Tebbs - Spokane WA, US
Kyle Sundin - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Blake Ballif - Greenacres WA, US
Brice Tebbs - Spokane WA, US
Kyle Sundin - Spokane WA, US
Assignee:
Signature Genomic Labs - Spokane WA
International Classification:
G06F 3/00, G06F 15/16, G06F 17/30, G06F 19/00
US Classification:
715751, 702 19, 707E17044
Abstract:
Techniques for allowing doctors and clinicians to upload genetic data associated with patients for comparison with previously-uploaded genetic data associated with other patients are described herein. These techniques may also allow doctors and clinicians to create notations associated with uploaded patient data. Both the previously-uploaded data as well as the created notations may be used by doctors and clinicians in attempting to diagnosis patients. That is, these techniques allow previously-acquired knowledge to be widely shared for the future benefit in attempting to detect genetic syndromes.
Methods And Systems For The Detection Of Microdeletion And Microduplication Syndromes
Methods And Systems For The Detection Of Microdeletion And Microduplication Syndromes
US Patent:
2009007, Mar 19, 2009
Filed:
Sep 16, 2008
Appl. No.:
12/211578
Inventors:
Bassem A. Bejjani - Spokane WA, US
Blake Charles Ballif - Greenacres WA, US
Lisa G. Shaffer - Spokane WA, US
Blake Charles Ballif - Greenacres WA, US
Lisa G. Shaffer - Spokane WA, US
Assignee:
SIGNATURE GENOMICS LABORATORIES, LLC - Spokane WA
International Classification:
C40B 30/04, C40B 40/08, C12Q 1/68
US Classification:
506 9, 506 17, 435 6
Abstract:
Methods for diagnosing the presence or absence of a genetic disorder in a patient are provided, wherein the genetic disorder is associated with a chromosomal abnormality at 1q41q42 and/or 16p11.2p12.2, and wherein the genetic disorder is not Fryns syndrome or congenital diaphragmatic hernia (CDH). Materials, such as microarrays for use in microarray CGH, and kits for use in such methods are also provided.
Interactive Genome Browser
Interactive Genome Browser
US Patent:
2010028, Nov 11, 2010
Filed:
Nov 6, 2009
Appl. No.:
12/614009
Inventors:
Brice Tebbs - Spokane WA, US
Blake C. Ballif - Greenacres WA, US
Bassem A. Bejjani - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Blake C. Ballif - Greenacres WA, US
Bassem A. Bejjani - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Assignee:
Signature Genomic Labs - Spokane WA
International Classification:
G06Q 50/00
US Classification:
705 2
Abstract:
Disclosed is an interactive genome browser executing within a web browser application, configured to display patient genetic data and additional genetic data tracks which are aligned by base pair. Additional tracks may include public data, community data, private data, sequence gaps, and additional genetic tests or probes which are available. Tests or probes may be ordered by selecting them from a test or probe track. Data in a genetic information database may also be searched using the interactive genome browser. Analyzed patient data may be published and made available to a community of users, which may communicate with one another.
Interactive Genome Browser
Interactive Genome Browser
US Patent:
2010028, Nov 4, 2010
Filed:
Nov 6, 2009
Appl. No.:
12/613978
Inventors:
Brice Tebbs - Spokane WA, US
Blake C. Ballif - Greenacres WA, US
Bassem A. Bejjani - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Blake C. Ballif - Greenacres WA, US
Bassem A. Bejjani - Spokane WA, US
Lisa G. Shaffer - Colbert WA, US
Assignee:
Signature Genomic Labs - Spokane WA
International Classification:
G06F 3/048, G06F 17/30, G06F 15/16
US Classification:
715760, 707769, 715771, 709203, 707E17014
Abstract:
Disclosed is an interactive genome browser executing within a web browser application, configured to display patient genetic data and additional genetic data tracks which are aligned by base pair. Additional tracks may include public data, community data, private data, sequence gaps, and additional genetic tests or probes which are available. Tests or probes may be ordered by selecting them from a test or probe track. Data in a genetic information database may also be searched using the interactive genome browser. Analyzed patient data may be published and made available to a community of users, which may communicate with one another.