Francis J. McMahon

ORCID: 0000-0002-9469-305X
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About
Contact & Profiles
Research Areas
  • Bipolar Disorder and Treatment
  • Genetic Associations and Epidemiology
  • Genetics and Neurodevelopmental Disorders
  • Genetic Syndromes and Imprinting
  • Genomic variations and chromosomal abnormalities
  • Adolescent and Pediatric Healthcare
  • Tryptophan and brain disorders
  • Genomics and Rare Diseases
  • Autism Spectrum Disorder Research
  • Treatment of Major Depression
  • Epigenetics and DNA Methylation
  • Child and Adolescent Psychosocial and Emotional Development
  • BRCA gene mutations in cancer
  • Genetic Neurodegenerative Diseases
  • Genetic Mapping and Diversity in Plants and Animals
  • Bioinformatics and Genomic Networks
  • Mental Health Research Topics
  • Functional Brain Connectivity Studies
  • Neurotransmitter Receptor Influence on Behavior
  • Suicide and Self-Harm Studies
  • Schizophrenia research and treatment
  • Congenital heart defects research
  • Attention Deficit Hyperactivity Disorder
  • Diet and metabolism studies
  • Stress Responses and Cortisol

National Institute of Mental Health
2016-2025

National Institutes of Health
2016-2025

United States Department of Health and Human Services
2015-2024

Institute of Human Genetics
2024

Dokkyo Medical University
2024

National Institute of Mental Health
2004-2023

National Institute of Mental Health
2019-2023

Genomics (United Kingdom)
2022

Spitalul Clinic de Psihiatrie Alexandru Obregia
2021

Center for Behavioral Brain Sciences
2021

Pamela Sklar Stephan Ripke Laura J. Scott Ole A. Andreassen Sven Cichon and 95 more Nick Craddock Howard J. Edenberg John I. Nürnberger Marcella Rietschel Douglas Blackwood Aiden Corvin Matthew Flickinger Weihua Guan Morten Mattingsdal Andrew McQuillin Phoenix Kwan Thomas F. Wienker Mark J. Daly Frank Dudbridge Peter Holmans Danyu Lin Margit Burmeister Tiffany A. Greenwood Marian L. Hamshere Pierandrea Muglia Erin N. Smith Peter P. Zandi Caroline M. Nievergelt R. Anne McKinney Paul D. Shilling Nicholas J. Schork Cinnamon S. Bloss Tatiana Foroud Daniel L. Koller Elliot S. Gershon Chunyu Liu Judith A. Badner William A. Scheftner William Lawson Evaristus A. Nwulia Maria Hipolito William Coryell John Rice William Byerley Francis J. McMahon Thomas G. Schulze Wade H. Berrettini Falk W. Lohoff James B. Potash Pamela B. Mahon Melvin G. McInnis Sebastian Zöllner Peng Zhang David W. Craig Szabocls Szelinger Thomas B. Barrett René Breuer Sandra Meier Jana Strohmaier Stephanie H. Witt Federica Tozzi Anne Farmer Peter McGuffin John S. Strauss Wei Xu Kristen M. Kennedy John B. Vincent K. Matthews Richard Day Manuel A. R. Ferreira Colm Ó'Dúshláine Roy H. Perlis Soumya Raychaudhuri Douglas M. Ruderfer Susan J. Lee Jordan W. Smoller Jun Li Devin Absher William E. Bunney Jack D. Barchas Alan F. Schatzberg Edward G. Jones Fan Meng Robert C. Thompson Stanley J. Watson Richard M. Myers Huda Akil Michael Boehnke Kim Chambert Jennifer L. Moran Ed Scolnick Srdjan Djurovic Ingrid Melle Gunnar Morken Michael Gill Derek W. Morris Emma M. Quinn Thomas W. Mühleisen Franziska Degenhardt Manuel Mattheisen

10.1038/ng.943 article EN Nature Genetics 2011-09-18

Nine cancer patients were treated with adoptive cell therapy using autologous anti-MAGE-A3 T-cell receptors (TCR)-engineered T cells. Five experienced clinical regression of their cancers including 2 on-going responders. Beginning 1–2 days postinfusion, 3 (#'s 5, 7, and 8) mental status changes, (5 lapsed into comas subsequently died. Magnetic resonance imagining analysis 5 8 demonstrated periventricular leukomalacia, examination brains at autopsy revealed necrotizing leukoencephalopathy...

10.1097/cji.0b013e3182829903 article EN Journal of Immunotherapy 2013-01-31
Mirko Manchia Mazda Adli Nirmala Akula Raffaella Ardau Jean-Michel Aubry and 95 more Lena Backlund Cláudio E. M. Banzato Bernhard T. Baune Frank Bellivier Susanne Bengesser Joanna M. Biernacka Clara Brichant‐Petitjean Elise T. Bui Cynthia Calkin Andrew Tai Ann Cheng Caterina Chillotti Sven Cichon Scott Clark Piotr M. Czerski Clarissa de Rosalmeida Dantas Maria Del Zompo J. Raymond DePaulo Sevilla D. Detera‐Wadleigh Bruno Étain Peter Falkai Louise Frisén Mark A. Frye Janice M. Fullerton Sébastien Gard Julie Garnham Fernando S. Goes Paul Grof Oliver Gruber Ryota Hashimoto Joanna Hauser Urs Heilbronner Rebecca Hoban Liping Hou Stéphane Jamain Jean‐Pierre Kahn Layla Kassem Tadafumi Kato John R. Kelsoe Sarah Kittel‐Schneider Sebastian Kliwicki Po‐Hsiu Kuo Ichiro Kusumi Gonzalo Laje Catharina Lavebratt Marion Leboyer Susan G. Leckband Carlos López‐Jaramillo Mario Maj Alain Malafosse Lina Martinsson Takuya Masui Philip B. Mitchell Frank Mondimore Palmiero Monteleone Audrey Nallet M. Neuner Tomáš Novák Claire O’Donovan Urban Ösby Norio Ozaki Roy H. Perlis Andrea Pfennig James B. Potash Daniela Reich‐Erkelenz Andreas Reif Eva Z. Reininghaus Sara Richardson Guy A. Rouleau Janusz Rybakowski Martin Schalling Peter R. Schofield Oliver Schubert Barbara Schweizer Florian Seemüller Maria Grigoroiu‐Serbânescu Giovanni Severino Lisa R. Seymour Claire Slaney Jordan W. Smoller Alessio Squassina Thomas Stamm Jo Steele Pavla Stopková Sarah K. Tighe Alfonso Tortorella Gustavo Turecki Naomi R. Wray A. Jordan Wright Peter P. Zandi David Zilles‐Wegner Michael Bauer Marcella Rietschel Francis J. McMahon Thomas G. Schulze Martin Alda

Objective The assessment of response to lithium maintenance treatment in bipolar disorder (BD) is complicated by variable length treatment, unpredictable clinical course, and often inconsistent compliance. Prospective retrospective methods have been proposed the literature. In this study we report key phenotypic measures “Retrospective Criteria Long-Term Treatment Response Research Subjects with Bipolar Disorder” scale currently used Consortium on Lithium Genetics (ConLiGen) study. Materials...

10.1371/journal.pone.0065636 article EN cc-by PLoS ONE 2013-06-19

Neuroinflammation is a pathological hallmark of Alzheimer's disease, but its role in cognitive impairment and course development during the disease are largely unknown. To address these unknowns, we used positron emission tomography with 11C-PBR28 to measure translocator protein 18 kDa (TSPO), putative biomarker for inflammation. Patients patients mild older control subjects were also scanned 11C-Pittsburgh Compound B amyloid burden. Twenty-nine amyloid-positive (19 Alzheimer's, 10...

10.1093/brain/awt145 article EN public-domain Brain 2013-06-17

Second-generation radioligands for translocator protein (TSPO), an inflammation marker, are confounded by the codominant rs6971 polymorphism that affects binding affinity. The resulting three groups homozygous high-affinity state (HH), low-affinity (LL), or heterozygous (HL). We tested if in vitro to leukocytes distinguished TSPO genotypes and genotype could affect clinical studies using radioligand [ 11 C]PBR28. In C]PBR28 brain imaging were performed 27 human subjects with known genotype....

10.1038/jcbfm.2012.131 article EN Journal of Cerebral Blood Flow & Metabolism 2012-09-12

A report on an initial genome screen 540 individuals in 97 families was collected as part of the NIMH Genetics Initiative Bipolar Disorder. Families were ascertained to be informative for genetic linkage and underwent a common ascertainment assessment protocol at four clinical sites. The sample genotyped 65 highly polymorphic markers from chromosomes 1, 6, 8, 10, 12. average intermarker interval 16 cM. Genotypic data analyzed using affected sib pair, multipoint pedigree analysis methods....

10.1002/(sici)1096-8628(19970531)74:3<247::aid-ajmg3>3.0.co;2-n article EN American Journal of Medical Genetics 1997-05-31

The HTTLPR, a functional polymorphism of the serotonin transporter gene solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 (SLC6A4), promoter, affects transcription and may be involved in antidepressant drug treatment outcome, although response rates with antidepressants can lower patients who experience adverse effects.To test hypothesis that HTTLPR is associated outcome to citalopram.A clinical effectiveness trial, Sequenced Treatment Alternatives Relieve...

10.1001/archpsyc.64.7.783 article EN Archives of General Psychiatry 2007-07-01

Suicidal ideation is an uncommon symptom than can emerge during antidepressant treatment. The biological basis of treatment-emergent suicidal unknown. Genetic markers may shed light on the causes and help identify individuals at high risk who benefit from closer monitoring, alternative treatments, or specialty care.A clinically representative cohort outpatients with major depressive disorder enrolled in Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial were treated...

10.1176/appi.ajp.2007.06122018 article EN American Journal of Psychiatry 2007-09-26
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