DR. FRANCIS J MCMAHON, MD
Psychiatric in Bethesda, MD

License number
Maryland D37624
Category
Psychiatric
Type
Psychiatry
Address
Address
35 Convent Dr ROOM 1A202, Bethesda, MD 20892
Phone
(301) 451-4453

Personal information

See more information about FRANCIS J MCMAHON at radaris.com
Name
Address
Phone
Francis Mcmahon
5705 Cromwell Dr, Bethesda, MD 20816
(301) 320-4214
Francis Mcmahon, age 64
5505 Charlcote Rd, Bethesda, MD 20817
(240) 731-2955
Francis Mcmahon
1127 Linden Ave, Halethorpe, MD 21227
(410) 242-0297
Francis X Mcmahon, age 92
17110 Longdraft Rd, Gaithersburg, MD 20878
(301) 208-1676
(301) 963-0311
(301) 963-4826

Organization information

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Francis J Mcmahon, MD

35 Convent Dr Room, Bethesda, MD

Industry:
Psychiatrist
Phone:
(301) 451-4453 (Phone)


Francis J McMahon MD

35 Convent Dr, Bethesda, MD 20892

Categories:
Physicians & Surgeons
Phone:
(301) 451-4453 (Phone)

Professional information

See more information about FRANCIS J MCMAHON at trustoria.com
Francis J Mcmahon Photo 1
Dr. Francis J Mcmahon, Bethesda MD - MD (Doctor of Medicine)

Dr. Francis J Mcmahon, Bethesda MD - MD (Doctor of Medicine)

Specialties:
Neuropsychiatry (Psychiatry)
Address:
National Institute Of Health
35 Convent Dr, Bethesda 20892
(301) 451-4453 (Phone)
Certifications:
Psychiatry, 1993
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
National Institute Of Health
35 Convent Dr, Bethesda 20892
Washington Adventist Hospital
7600 Carroll Ave, Takoma Park 20912
Education:
Medical School
Johns Hopkins University / School of Medicine
Graduated: 1987
Francis Scott Key Med Ctr
The Johns Hopkins Hospital


Francis Mcmahon Photo 2
Chief, Human Genetics Branch At National Institute Of Mental Health

Chief, Human Genetics Branch At National Institute Of Mental Health

Position:
Chief, Human Genetics Branch at National Institute of Mental Health
Location:
Washington D.C. Metro Area
Industry:
Research
Work:
National Institute of Mental Health - United States since Sep 2010 - Chief, Human Genetics Branch National Institutes of Health - Bethesda, MD 2002 - 2010 - Chief, Unit on Genetic Basis of Mood & Anxiety Disorders University of Chicago 1998 - 2002 - Associate Professor Johns Hopkins School of Medicine - Baltimore, Maryland Area 1991 - 1998 - Faculty
Education:
The Johns Hopkins University School of Medicine 1983 - 1987
MD
University of Pennsylvania 1978 - 1982
BA, Biology


Francis Mcmahon Photo 3
Methods To Identify Patients At Risk Of Developing Adverse Events During Treatment With Antidepressant Medication

Methods To Identify Patients At Risk Of Developing Adverse Events During Treatment With Antidepressant Medication

US Patent:
7906283, Mar 15, 2011
Filed:
Oct 26, 2007
Appl. No.:
11/925334
Inventors:
Francis J. McMahon - Bethesda MD, US
Gonzalo E. Laje - Potomac MD, US
Silvia Paddock - Solna, SE
Husseini K. Manji - Cabin John MD, US
A. John Rush - Dallas TX, US
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC
Board of Regents, the University of Texas System - Austin IL
International Classification:
C12Q 1/68, C12P 19/34, C07H 21/02, C07H 21/04
US Classification:
435 6, 435 912, 536 235, 536 2431
Abstract:
The invention provides a method of screening patients to identify those patients more likely to exhibit an increased risk of treatment-emergent suicidal ideation comprising: (a) obtaining a sample of genetic material from the patients, and (b) assaying the sample for the presence of a genotype in the patients which is associated with an increased risk of treatment-emergent suicidal ideation, wherein the genotype is characterized by a polymorphism in a gene selected from the group consisting of glutamine receptor, ionotropic, kainate 2 (GRIK2); glutamate receptor ionotropic AMPA 3 (GRIA3); and combinations thereof.


Francis Mcmahon Photo 4
Methods To Predict The Outcome Of Treatment With Antidepressant Medication

Methods To Predict The Outcome Of Treatment With Antidepressant Medication

US Patent:
2008023, Sep 25, 2008
Filed:
Mar 19, 2008
Appl. No.:
12/051494
Inventors:
Francis J. McMahon - Bethesda MD, US
Gonzalo E. Laje - Potomac MD, US
Silvia Paddock - Solna, SE
Husseini K. Manji - Cabin John MD, US
Alexander F. Wilson - Phoenix MD, US
Assignee:
Gov. of the United States of America, represented by the Secretary, Dept. of Health and - Rockville MD
Board fo Regents, The University of Texas System - Austin TX
International Classification:
G01N 33/50
US Classification:
436 94
Abstract:
The invention provides a method for determining the outcome of treatment with an antidepressant medication in a patient. In particular, the invention provides a method of screening patients to identify those patients with a decreased risk of non-response to treatment with antidepressant medication comprising: (a) obtaining a sample of genetic material from the patients, and (b) assaying the sample for the presence of a genotype in the patients which is associated with a decreased risk of non-response to treatment with antidepressant medication, wherein the genotype is characterized by a polymorphism in a HTR2A, GRIK4, BCL2, or a combination thereof.


Francis Mcmahon Photo 5
Methods To Identify Patients At Risk Of Developing Adverse Events During Treatment With Antidepressant Medication

Methods To Identify Patients At Risk Of Developing Adverse Events During Treatment With Antidepressant Medication

US Patent:
2011011, May 19, 2011
Filed:
Jan 27, 2011
Appl. No.:
13/015068
Inventors:
Francis J. McMahon - Bethesda MD, US
Gonzalo E. Laje - Potomac MD, US
Silvia Paddock - Solna, SE
Husseini K. Manji - Cabin John MD, US
A. John Rush - Dallas TX, US
Assignee:
The United States of America, Represented by the Secretary, Department of Health - Bethesda MD
BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM - Austin TX
International Classification:
C40B 30/00
US Classification:
506 7
Abstract:
The invention provides a method of screening patients to identify those patients more likely to exhibit an increased risk of treatment-emergent suicidal ideation comprising: (a) obtaining a sample of genetic material from the patients, and (b) assaying the sample for the presence of a genotype in the patients which is associated with an increased risk of treatment-emergent suicidal ideation, wherein the genotype is characterized by a polymorphism in a gene selected from the group consisting of glutamine receptor, ionotropic, kainate 2 (GRIK2); glutamate receptor ionotropic AMPA 3 (GRIA3); and combinations thereof.