Michael Barmada | Academic Influence

Michael Barmada's AcademicInfluence.com Rankings

Michael Barmada

Biology

#14788

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#18640

Historical Rank

Genetics

#1703

World Rank

#1813

Historical Rank

Molecular Biology

#2665

World Rank

#2706

Historical Rank

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Biology

Michael Barmada's Degrees

Bachelors Biology University of California, Berkeley
PhD Genetics Stanford University

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Why Is Michael Barmada Influential?

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According to Wikipedia, Mahmud Barmada, known as Michael Barmada, was an American geneticist. He was a Distinguished Professor at the University of Pittsburgh School of Medicine. Career Barmada worked at the Institute for Personalized Medicine as associate director and co-director of the Center for Simulation and Modeling. He held a secondary appointment in the Department of Biomedical Informatics.

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Michael Barmada's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene (2006) (2867)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) (2621)
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis (2007) (1825)
Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease (2011) (1656)
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis. (2000) (492)
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy (2002) (424)
Alcohol consumption, cigarette smoking, and the risk of recurrent acute and chronic pancreatitis. (2009) (401)
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis (2012) (308)
Common variants at MS 4 A 4 / MS 4 A 6 E , CD 2 AP , CD 33 and EPHA 1 are associated with late-onset Alzheimer ’ s disease (2011) (274)
Type of pain, pain-associated complications, quality of life, disability and resource utilisation in chronic pancreatitis: a prospective cohort study (2010) (267)
Hereditary lymphedema: evidence for linkage and genetic heterogeneity. (1998) (250)
Clinical and Molecular Heterogeneity in the Brugada Syndrome: A Novel Gene Locus on Chromosome 3 (2002) (249)
Multicenter Approach to Recurrent Acute and Chronic Pancreatitis in the United States: The North American Pancreatitis Study 2 (NAPS2) (2008) (225)
Genome-wide association study of Alzheimer's disease (2012) (220)
High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12. (2000) (203)
Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. (2012) (202)
Ulcerative colitis loci on chromosomes 1p36 and 12q15 identified by genome-wide association study (2008) (199)
A new locus for hemiplegic migraine maps to chromosome 1q31 (1997) (198)
SPINK1/PSTI mutations are associated with tropical pancreatitis and type II diabetes mellitus in Bangladesh. (2002) (158)
High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy (2012) (158)
Linkage and association between inflammatory bowel disease and a locus on chromosome 12. (1998) (155)
Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis (2014) (152)
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. (2014) (140)
Combined bicarbonate conductance-impairing variants in CFTR and SPINK1 variants are associated with chronic pancreatitis in patients without cystic fibrosis. (2011) (138)
Pathways to Injury in Chronic Pancreatitis: Decoding the Role of the High-Risk SPINK1 N34S Haplotype Using Meta-Analysis (2008) (128)
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3. (1999) (116)
Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms (2011) (114)
Learning genetic epistasis using Bayesian network scoring criteria (2011) (105)
The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn disease. (2000) (95)
Genome-wide association analysis of age-at-onset in Alzheimer's disease (2012) (93)
Physical and Mental Quality of Life in Chronic Pancreatitis: A Case-Control Study From the North American Pancreatitis Study 2 Cohort (2013) (88)
African ancestry and lung function in Puerto Rican children. (2012) (86)
Congenital motor nystagmus linked to Xq26-q27. (1999) (85)
Association of CLU and PICALM variants with Alzheimer's disease (2012) (84)
Is the monocyte chemotactic protein-1 -2518 G allele a risk factor for severe acute pancreatitis? (2005) (80)
A Genome Scan in 260 Inflammatory Bowel Disease-Affected Relative Pairs (2004) (77)
Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. (2004) (74)
Heritability of and mortality prediction with a longevity phenotype: the healthy aging index. (2014) (71)
Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study (2009) (71)
Genetic and environmental influences on thyroid hormone variation in Mexican Americans. (2004) (68)
The IBD International Genetics Consortium Provides Further Evidence for Linkage to IBD4 and Shows Gene‐Environment Interaction (2005) (67)
Limited Contribution of the SPINK1 N34S Mutation to the Risk and Severity of Alcoholic Chronic Pancreatitis: A Report from the United States (2003) (66)
Significant association between ABO blood group and pancreatic cancer. (2010) (66)
A gene for autosomal dominant congenital nystagmus localizes to 6p12. (1996) (62)
Identifying genetic interactions in genome‐wide data using Bayesian networks (2010) (59)
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment (2006) (58)
TCGA Expedition: A Data Acquisition and Management System for TCGA Data (2016) (57)
Genetic determinants of disease progression in Alzheimer's disease. (2014) (53)
Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12 (2002) (51)
Comprehensive Analysis of HLA-G: Implications for Recurrent Spontaneous Abortion (2010) (45)
Age-at-Onset in Late Onset Alzheimer Disease is Modified by Multiple Genetic Loci (2014) (44)
Does the pain-protective GTP cyclohydrolase haplotype significantly alter the pattern or severity of pain in humans with chronic pancreatitis? (2008) (44)
Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings (2014) (43)
Pooling-Based Genome-Wide Association Study Implicates Gamma-Glutamyltransferase 1 (GGT1) Gene in Pancreatic Carcinogenesis (2010) (43)
Genetics of gastroesophageal reflux disease: a review. (2002) (42)
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels (2003) (41)
Whole exome sequencing identifies multiple, complex etiologies in an idiopathic hereditary pancreatitis kindred. (2012) (41)
Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations. (2013) (41)
Rarity of the Alzheimer disease-protective APP A673T variant in the United States. (2015) (39)
Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. (2004) (39)
Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado. (2007) (39)
Protease-Sensitive Pancreatic Lipase Variants Are Associated With Early Onset Chronic Pancreatitis. (2019) (38)
Physical activity levels in American-Indian adults: the Strong Heart Family Study. (2009) (37)
Evidence for an inflammatory bowel disease locus on chromosome 3p26: linkage, transmission/disequilibrium and partitioning of linkage. (2002) (37)
Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations (2004) (36)
Analysis of tumor necrosis factor-α, transforming growth factor-β1, interleukin-10, and interferon-γ polymorphisms in patients with alcoholic chronic pancreatitis (2004) (35)
Phenotype-Stratified Genetic Linkage Study Demonstrates that IBD2 Is an Extensive Ulcerative Colitis Locus (2006) (35)
Parental attitudes toward newborn screening for Duchenne/Becker muscular dystrophy and spinal muscular atrophy (2014) (32)
A Bayesian Method for Evaluating and Discovering Disease Loci Associations (2011) (32)
A fast algorithm for learning epistatic genomic relationships. (2010) (31)
X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping (2007) (30)
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13 (2003) (30)
The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. (2005) (30)
Genetic Variation in C-Reactive Protein (CRP) Gene May Be Associated with Risk of Systemic Lupus Erythematosus and CRP Concentrations (2008) (29)
An efficient bayesian method for predicting clinical outcomes from genome-wide data. (2010) (28)
Prostaglandin E2 and IL‐23 plus IL‐1β Differentially Regulate the Th1/Th17 Immune Response of Human CD161+CD4+ Memory T Cells (2011) (27)
The PPARγ Pro12Ala Polymorphism Is Not Associated with Body Mass Index or Waist Circumference among Hispanics from Colorado (2007) (26)
Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection. (2008) (26)
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry (2016) (26)
Genome-Wide Association Study of Antiphospholipid Antibodies (2013) (26)
Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families (2002) (25)
Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24. (2003) (25)
Evaluating Disorders with a Complex Genetics Basis. The Future Roles of Meta-analysis and Systems Biology (2005) (25)
The Serotonin Transporter: Sequence Variation in Macaca fascicularis and its Relationship to Dominance (2007) (25)
Analysis of tumor necrosis factor-alpha, transforming growth factor-beta 1, interleukin-10, and interferon-gamma polymorphisms in patients with alcoholic chronic pancreatitis. (2004) (24)
African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32. (2003) (24)
Beta-amyloid toxicity modifier genes and the risk of Alzheimer's disease. (2012) (24)
“Predicting” parental longevity from offspring endophenotypes: Data from the Long Life Family Study (LLFS) (2010) (22)
A genome scan in 260 inflammatory bowel disease-affected relative pairs. (2004) (22)
Lipoprotein lipase gene sequencing and plasma lipid profile[S] (2014) (21)
The functional angiotensin converting enzyme gene I/D polymorphism does not alter susceptibility to chronic pancreatitis. (2004) (21)
Comprehensive Evaluation of the Association of APOE Genetic Variation with Plasma Lipoprotein Traits in U.S. Whites and African Blacks (2014) (21)
Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis (2004) (21)
The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado. (2007) (19)
Keratin 8 Mutations Are Not Associated with Familial, Sporadic and Alcoholic Pancreatitis in a Population from the United States (2006) (19)
Impact of Genetic Variants in Human Scavenger Receptor Class B Type I (SCARB1) on Plasma Lipid Traits (2014) (18)
A Bayesian Method for Identifying Genetic Interactions (2009) (18)
A systems biology approach to genetic studies of pancreatitis and other complex diseases. (2007) (18)
A Novel Locus for Familial Migraine on Xp22 (2010) (18)
Genomewide Association Analysis of Respiratory Syncytial Virus Infection in Mice (2009) (18)
A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease (2014) (17)
The application of network label propagation to rank biomarkers in genome-wide Alzheimer’s data (2014) (17)
Genome-Wide Association Study and Linkage Analysis of the Healthy Aging Index. (2015) (16)
Clinical and Molecular Heterogeneity in the Brugada Syndrome (2002) (16)
Identifying genetic interactions associated with late-onset Alzheimer’s disease (2014) (15)
Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α ( TNF -α) promoter region or the TNF receptor 1 ( TNFR1 ) gene (2003) (15)
Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice. (2014) (14)
Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study (2015) (14)
Functional Polymorphisms of the Coagulation Factor II Gene (F2) and Susceptibility to Systemic Lupus Erythematosus (2011) (14)
Genetic association and differential expression of PITX2 with acute appendicitis (2018) (13)
Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels. (2016) (12)
Association of MHC region SNPs with irritant susceptibility in healthcare workers (2016) (12)
Needs Assessment for Research Use of High-Throughput Sequencing at a Large Academic Medical Center (2015) (11)
Genome-wide association study identifies five novel susceptibility loci for Crohn ' s disease and implicates a role for autophagy in disease pathogenesis (2009) (11)
Genetic studies of diseases (2007) (11)
Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. (2015) (10)
Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor alpha (TNF-alpha) promoter region or the TNF receptor 1 (TNFR1) gene. (2003) (10)
MHC recombinant families (1997) (10)
Resequencing of LPL in African Blacks and associations with lipoprotein–lipid levels (2015) (9)
The MCP-1 –2518 A/G Polymorphism Is Not a Susceptibility Factor for Chronic Pancreatitis (2006) (9)
Replication of European Rheumatoid Arthritis Loci in a Pakistani Population (2013) (8)
Transforming growth factor-beta1, interleukin-10 and interferon-gamma cytokine polymorphisms in patients with hereditary, familial and sporadic chronic pancreatitis. (2004) (7)
Autosomal dominant infant GERD: Exclusion of a 13q14 locus in 6 well-characterized families suggests genetic heterogeneity (2001) (7)
Associating Symptom Phenotype and Genotype in Preeclampsia (2018) (7)
Ulcerative colitis is more strongly linked to chromosome 12 than Crohn's disease (2001) (7)
S2091 Does the Pain-Protective GTP Cyclohydrolase Haplotype Significantly Alter the Severity of Pain in Humans with Chronic Pancreatitis? (2008) (7)
Transforming Growth Factor-β1, Interleukin-10 and Interferon-γ Cytokine Polymorphisms in Patients with Hereditary, Familial and Sporadic Chronic Pancreatitis (2004) (7)
Challenges of examining complex genetic disorders like GERD. (2005) (6)
Genetic Basis of Irritant Susceptibility in Health Care Workers (2016) (6)
SPINK 1 mutations modify phenotypic expression in hereditary pancreatitis (HP) caused by cationic trypsinogen (PRSS1) mutations R122H and N291 (2001) (6)
Hereditary, familial, and idiopathic chronic pancreatitis are not associated with polymorphisms in the tumor necrosis factor α (TNF-α) promoter region or the TNF receptor 1 (TNFR1) gene (2003) (5)
Perinuclear neutrophil antibodies are not markers for genetic susceptibility or indicators of genetic heterogeneity in familial ulcerative colitis (2002) (5)
The IBD4 locus shows linkage heterogeneity between Crohn's disease and ulcerative colitis (2001) (4)
Baller-Gerold syndrome: a postmortem examination. (1993) (3)
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USA (2005) (3)
THE MCP-1 -2518 G ALLELE ACTS AS A POTENT DISEASE SEVERITY MODIFIER IN ACUTE PANCREATITIS. (2004) (3)
The universal genetics database: infor- mation sharing in genetics and beyond (2006) (2)
Transmission/disequilibrium test analysis of a genome scan dataset detects a novel, significant inflammatory bowel disease linkage to chromosome 3p (2001) (2)
Biogenetic mechanisms predisposing to complex phenotypes in parents may function differently in their children. (2013) (2)
Perinuclear neutrophil antibodies are not markers for genetic susceptibility or indicators of genetic heterogeneity in familial ulcerative colitis. (2002) (2)
A Two Locus Model for Hemiplegic Migraine on Chr1q and Candidate Gene Screening (1998) (2)
Stability of exploratory multivariate data modeling in longitudinal data (2003) (2)
475o Resistin, a Potent Adipokine, is Associated With Acute Pancreatitis: Assessment of Functional Genetic Polymorphisms and Serum Levels (2010) (1)
Integrative Systems Biology: Implications for the Understanding of Human Disease (2009) (1)
The application of network label propagation to rank biomarkers in genome-wide Alzheimer’s data (2014) (1)
Evaluating de novo locus-disease discoveries in GWAS using the signal-to-noise ratio. (2011) (1)
X-linked lethal infantile (XL)-SMA: new clinical information, variant phenotypes, and candidate disease gene studies. (2004) (1)
Abstract 21122: Contribution of ABCA1 Genetic Variation to Plasma Lipid Levels in Non-Hispanic White Americans (2017) (1)
S2090 SPINK1 N34s Is Not Associated with the Sentinel Acute Pancreatitis Episode But Predisposes Patients to Recurrent Attacks (2008) (1)
Characteristics of microsatellite markers in the HLA region of the old order Amish: recombination hotspots and other findings. (1996) (0)
Correction: Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis (2014) (0)
The SPINKI N34S mutation is not associated with type 2 diabetes mellitus in the united states (2003) (0)
KERATIN 8 MUTATIONS ARE NOT ASSOCIATED WITH HEREDITARY OR ALCOHOLIC CHRONIC PANCREATITIS IN THE UNITED STATES. (2004) (0)
Identifying genetic interactions associated with late-onset Alzheimer’s disease (2014) (0)
Publicly available NGS datasets used for analysis ( Current Users ). (2015) (0)
S1320 Alcohol and Smoking Are Independent Predictors for Chronic Pancreatitis (2008) (0)
Variation in SPINK-1 N34S Effect Size Is Population-Dependant: 209 (2006) (0)
High-density genome scan in Crohn's disease shows linkage to chromosome 14Q and linkage and association with chromosome 3P (2000) (0)
Association of Gamma-Glutamyltransferase 1 Gene (GGT1) Polymorphisms With Idiopathic Chronic Pancreatitis in the NAPS2 Cohort (2011) (0)
Research objectives of survey respondents (All Users). (2015) (0)
Prevalence of the N34S Mutation in Patients with Acute Pancreatitis: 201 (2006) (0)
Teaching Course I: Behavioural Aspects of Headache Management - State of the Art and Science (2001) (0)
Automated typing of fluorescent microsatellite markers: technical aspects (1994) (0)
Prevalence of the Calcium Sensing Receptor (CaSR) Gene Polymorphisms in Patients with Recurrent Acute and Chronic Pancreatitis with or without SPINK1 N34S: 212 (2007) (0)
African Ancestry, SES, FEV1 And Asthma Exacerbations In Puerto Rican Children (2012) (0)
A genome scan at 751 microsatellite loci reveals linkage between Crohn's disease and chromosome 14q11–12, the IBD4 locus (2000) (0)
S1315 Immunohistochemical Staining of the Pancreas with TGF-β1, MMP-2 and TIMP-2 in Patients with Autoimmune Chronic Pancreatitis and Alcoholic Chronic Pancreatitis (0)
Identifying Genetic Interactions Associated with La te-Onset 1 (2013) (0)
Brief communication Association of CLU and PICALM variants with Alzheimer's disease (2012) (0)
Hyperthyroidism with thick-filament loss: evidence for a myopathic pathogenesis (1996) (0)
An examination of regulatory function for GWAS-confirmed and suggestive loci of late-onset Alzheimer's disease (2013) (0)
Duplication of a 303 kb Locus Containing PRSS1 and PRSS2 is Associated With Hereditary Pancreatitis in a Spanish Kindred (2011) (0)
Chapter 10 – Integrative Systems Biology: Implications for the Understanding of Human Disease (2009) (0)
S1314 Chronic Pancreatitis Characterized By Constant Pain Regardless of Severity Is Associated with Poorer Quality of Life, Lower Functioning and Increased Utilization of Resources (2008) (0)
A comprehensive association study of apolipoprotein E-C1-C4-C2 gene cluster variation with plasma lipoprotein traits. (2017) (0)
SPINKI mutations are associated with an earlier age at onset in patients with idiopathic chronic pancreatitis (2003) (0)
Rare/uncommon (MAF<5%) variants analysis with lipid traits in African Blacks. (2014) (0)
9th Meeting of the Spanish Bilio-Pancreatic Club (2006) (0)
Acute pancreatitis precedes chronic pancreatitis in the majority of patients: Results from the NAPS2 consortium. (2022) (0)
Contribution of the Pro12Ala Polymorphism of PPARγ To Risk of Type 2 Diabetes Stratifie d by Behavior (2002) (0)
Subject Index Vol. 4, 2004 (2004) (0)
Genetic association and differential expression of PITX2 with acute appendicitis (2018) (0)
JAMA Peer Reviewers in 2018. (2019) (0)
Genetic variants associated with PDAC also contribute to chronic pancreatitis susceptibility (2015) (0)
IAP Membership Application Form 2010 (2010) (0)
M1871 Use of Mathematical and Statistical Model Predictions to Identify a Novel Pancreas-Specific Class of CFTR Variants Linked to SPINK1 Mutations and Idiopathic Chronic Pancreatitis (2010) (0)
Genetic determinants of progression of Alzheimer's disease (2013) (0)
Contents Vol. 4, 2004 (2004) (0)
Whole Genome Association Identifies Novel Susceptibility Genes for Crohn's Disease and Implicates a Crucial Role for Autophagy (2007) (0)
Abstract 16678: Multigenic Etiology of CHD With Heterotaxy Involving PCD and Cilia Genes (2011) (0)
UPC Society News (2008) (0)
Mathematical modeling of trypsin activation in acinar cell environment (2013) (0)
P365 – Allelic variation of nine microsatellite markers on chromosome 6 in the OLD order amish (1996) (0)

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