Naftali Kaminski, MD
Cards
Research
About
Professional Highlights
Contact/Administration
Research
About
Professional Highlights
Contact/Administration
Research
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Honors
- 7 International Awards
- 4 National Awards
- 1 Regional Award
Activities
- 96 Activities
- 2013 - Present
- 8 Countries
Contact Info
Pulmonary, Critical Care & Sleep Medicine
300 Cedar Street, TAC-441 South, PO Box 208057
New Haven, CT 06520-8057
United States
Administrative Support
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine
Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Appointments
Education
Hadassah Medical School, The Hebrew University (1990)
Hebrew University (1989)
Hebrew University (1985)
Honors
- 7 International Awards
- 4 National Awards
- 1 Regional Award
Activities
- 96 Activities
- 2013 - Present
- 8 Countries
Contact Info
Pulmonary, Critical Care & Sleep Medicine
300 Cedar Street, TAC-441 South, PO Box 208057
New Haven, CT 06520-8057
United States
Administrative Support
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
Publications Overview
- 545 Publications
- 48,865 Citations
- 169 Yale Co-Authors
The Kaminski Lab
About
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Titles
Boehringer Ingelheim Pharmaceuticals, Inc. Professor of Medicine (Pulmonary)
Director of Center for Pulmonary Injury, Repair and Therapeutics (CPIRT) , Pulmonary, Critical Care & Sleep Medicine; Co-director of the Clinical Investigation (CI) concentration within the Master of Health Science (MHS) degree , Medical Education
Biography
Dr. Naftali Kaminski is the Boehringer-Ingelheim Endowed Professor of Internal Medicine and Director of the Center of Pulmonary Injury, Repair and Therapeutics (CPIRT) at Yale's Pulmonary, Critical Care and Sleep Medicine (Yale PCCSM). He served as Chief of Yale PCCSM from 2013–2026. Before that he was a tenured professor of Medicine, Pathology, Computational Biology and Human Genetics, and the Dorothy P. and Richard P. Simmons Endowed Chair for Pulmonary Research at the University of Pittsburgh. Dr. Kaminski was the director of the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease and the Lung, Blood and Vascular Center for Genomic Medicine at the Division of Pulmonary, Allergy and Critical Care Medicine at the University of Pittsburgh.
Dr. Kaminski received his medical degree from the Hebrew University - Hadassah Medical School in Jerusalem, Israel, and completed a residency in Internal Medicine at Hadassah Mount-Scopus University Hospital in Jerusalem, and a fellowship in pulmonary medicine at Sheba Medical Center in Tel-Hashomer, Israel. Dr. Kaminski received his basic science training in Dean Sheppard's laboratory at the Lung Biology Center at UCSF and in functional genomics and microarray technology at the Functional Genomics laboratory at Roche Bioscience, Palo-Alto. After his fellowship in 2000, Dr. Kaminski was appointed head of Functional Genomics at Sheba Medical Center in Israel, before being recruited to head the Simmons Center at the University of Pittsburgh in 2002.
Dr. Kaminski's main research interests involve applying genomic approaches to elucidate basic mechanisms and improve diagnosis and treatment of Idiopathic Pulmonary Fibrosis (IPF), a chronic, mostly lethal, and currently untreatable scarring lung disease, and other chronic lung diseases such as Chronic Obstructive Pulmonary Disease (COPD), severe asthma, and sarcoidosis. His group pioneered the application of high-throughput genome-scale transcript profiling in advanced lung disease. Among his key scientific achievements are: The discovery of novel molecules with significant active roles in pulmonary fibrosis, including matrix metalloproteases (MMP7, MMP19) and phosphatases (SHP2, MKP5) , demonstrating that microRNAs, a family of small non-coding RNAs, are differentially expressed in IPF, and that some of them (let-7, mir-29, mir-33) are mechanistically involved in lung fibrosis, and the discovery that the outcome of patients with IPF can be predicted based on the expression of peripheral blood proteins and genes, a finding with practical implication because of the need for risk stratification and transplant prioritization. Dr. Kaminski's team identified a potential antifibrotic role for thyroid hormone signaling, a novel discovery with significant therapeutic implications. Dr. Kaminski's is among the world leading teams in single cell profiling of lung diseases. They ahve made substantial discoveries including the aberrant basaloid cells, alveolar epithelial cells that express some markers of airway basal cells, EMT, senescenece and known activators and biomarkers of fibrosis. To democratize access to these data, they created the IPF Cell Atlas (www.IPFCellAtlas.com), now a widely used global resource, along with companion portals for the Normal Lung Endothelial Cell Atlas, COPD Cell Atlas, and Normal Lung Aging Cell Atlas, establishing an open, interoperable foundation for precision lung medicine. Dr. Kaminski has a strong interest in integrating high throughput ‘omics’ data, such as genome scale DNA variants, coding and non-coding RNAs, microbiome and metabolome information with clinical information to generate systems biology models of lung diseases and to develop precision medicine approaches that are significantly more precise, predictive and patient-centered than anything that is currently available.
Since completing his clinical training, Dr. Kaminski authored more than 450 research papers (including in Nature Medicine, NEJM, Nature Genetics, Nature Communications, Nature Biomedical Engineering, NAS, Science Advances, Science Translational Medicine, Circulation, Lancet Respiratory Medicine, ARCCM and ERJ among others) review articles and book chapters and has given numerous invited talks at national and international conferences, review articles and book chapters and has given numerous invited talks at national and International conferences. Since he finished his fellowship in 2000, Dr. Kaminski has been consistently funded by NIH and is the PI of multiple NIH grants. Dr. Kaminski's work and impact have been recognized rationally and internationally and among his awards are the Morgagni Award for Scientific Research from Morgagni Pulmonary Disease Association,in Italy, the Trudeau Honorary Lecture of New York State Thoracic Society, American Thoracic Society (ATS) Amberson Lecture Award, the Coalition for Pulmonary Fibrosis Marvin Schwarz Award for Pulmonary Fibrosis, the ATS Recognition of Scientific Achievements award, the Helmholtz Institute International Fellow Award, the European Respiratory Society Gold Medal for Interstitial Lung Disease, as well as numerous named hornorary lectures. Kaminskii is also an elected member of the Association of American Physicians, and the Connecticut Academy of Science and Engineering.
Dr. Kaminski was active on the ATS and was the editor of “Gene Express”, a column on genomics in the initial days of the ATS Website, a member and chair of the Program Committee of the Assembly on Respiratory Cell and Molecular Biology of the ATS, and member of the ATS Research Advocacy Committee, and Chair of the Assembly on Respiratory, Cell, and Molecular Biology at the American Thoracic Society. He was an associate editor of the American Journal of Respiratory and Critical care Medicine, a member of multiple editorial boards and recently the Deputy Editor of Thorax, BMJ. Dr. Kaminski served as the President of the Association of Pulmonary, Critical Care and Sleep Division Directors .
Dr. Kaminski is passionate about training physician-scientists and resepiratory researchers for the challenges of 21st century medicine, and especially in the vocabulary, skills and technology of the new fields of single cell genomics, bioinformatics, computational and system biology and their application to understanding the basic mechanisms that govern lung health and disease as well as to designed personalized medicine approaches. Dr. Kaminski is the contact PI and director of the highly successful NIH NHLBI “Training in Translational Lung Biology and Pathobiology“ T32 grant at Yale. He has successfully mentored over 50 mentees, many of whom are highly accomplished, independently funded researchers and academic and industry leaders. has mentored multiple MD and PhD scientists, of them many have productive and well funded independent career. H
Appointments
Pulmonary, Critical Care & Sleep Medicine
ProfessorPrimaryEnvironmental Health Sciences
ProfessorSecondaryPharmacology
ProfessorSecondary
Other Departments & Organizations
- Center for RNA Science and Medicine
- Computational Biology and Biomedical Informatics
- CPIRT - Center for Pulmonary Injury, Repair, and Therapeutics
- Environmental Health Sciences
- Internal Medicine
- Interstitial Lung Disease (ILD) Program
- Kaminski Lab
- MHS-CI Program Leadership
- Molecular Medicine, Pharmacology, and Physiology
- Pharmacology
- Program in Translational Biomedicine (PTB)
- Pulmonary, Critical Care & Sleep Medicine
- The Center for Precision Pulmonary Medicine (P2MED)
- Yale Combined Program in the Biological and Biomedical Sciences (BBS)
- Yale Fibrosis Program
- Yale Medicine
- Yale New Haven Health System
- Yale Stem Cell Center
- Yale-BI Biomedical Data Science Fellowship
Education & Training
- MD
- Hadassah Medical School, The Hebrew University (1990)
- MD
- Hebrew University (1989)
- BM
- Hebrew University (1985)
Research
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Overview
Dr. Kaminski’s team main ambition is to uncover the mechanisms, and thus have a significant impact on the management of advanced lung diseases with a specific focus on IPF, a chronic progressive interstitial lung disease that is currently incurable. To study these mechanisms Dr. Kaminski’s team applies systems biology approaches that incorporate a combination of traditional molecular biology methods, high-throughput genomic technologies such as transcript level profiling (single cell RNA sequencing and epigenomic profiling ) , genome scale analyses of gene variants, advanced bioinformatics approaches and targeted proteomic approaches. These studies have led to shifts in the perception of pulmonary fibrosis, the realization that aberrant activation of developmental pathways is at the core of lung fibrosis, the discovery of the role of microRNAs in IPF, the identification and validation of novel prognostic biomarkers in the bloodstream, as well many additional insights.
Mechanisms of pulmonary fibrosis and other chronic lung diseases
- Understanding and identifying the genetic and molecular networks that determine the lung phenotype using high throughput high resolution genomic and proteomic technologies.
- Role of miRNA in advanced lung disease (IPF, Emphysema).
- Role of other non-coding RNAs (lincRNAs) in advanced lung disease
- The IPF Cell Atlas (www.IPFCellAtlas.com)
- The Normal Aging Lung Cell Atlas
- The Pulmonary Fibrosis Connectome
- Epigenomics of chronic lung disease.
- Using AI to Integrate clinical, biological, genomic and proteomic data to identify new molecular phenotypes of disease.
New molecular targets in Pulmonary Fibrosis
- The role and regulation of microRNAs (let-7, mir-33, mir-29) in human pulmonary fibrosis and development of microRNA inhibitors and agonist for therapeutic interventions
- The role of large non-coding RNAs in pulmonary fibrosis
- Role of GPR87 in Pulmonary fibrosis
- The role of thyroid hormone signaling in epithelial cell protection in fibrosis
- Origin and role of Aberrant Basaloid Cells
- Novel lung resident cell specific therapeutic approaches in pulmonary fibrosis
Biomarker Discovery and Validation in chronic and progressive lung disease
- Approaches to the development of liquid biopsy in human pulmonary fibrosis and other interstitial lung disease
- Immune cells in interstitial lung diseaes
- Peripheral blood protein markers in lung fibrosis
- Genetic predictors of outcome in lung fibrosis
- Peripheral blood gene expression changes and disease progression
Medical Research Interests
Public Health Interests
ORCID
0000-0001-5917-4601- View Lab Website
The Kaminski Lab
Research at a Glance
Yale Co-Authors
Publications Timeline
Research Interests
Taylor Adams
Farida Ahangari, MD
Jonas Christian Schupp, MD
Xiting Yan, PhD
Erica Herzog, MD, PhD
Robert Homer, MD, PhD
Idiopathic Pulmonary Fibrosis
Pulmonary Fibrosis
Gene Expression
MicroRNAs
Genomics
Lung Diseases
Publications
Featured Publications
A lung targeted miR-29 mimic as a therapy for pulmonary fibrosis
Chioccioli M, Roy S, Newell R, Pestano L, Dickinson B, Rigby K, Herazo-Maya J, Jenkins G, Ian S, Saini G, Johnson SR, Braybrooke R, Yu G, Sauler M, Ahangari F, Ding S, DeIuliis J, Aurelien N, Montgomery RL, Kaminski N. A lung targeted miR-29 mimic as a therapy for pulmonary fibrosis. EBioMedicine 2022, 85: 104304. PMID: 36265417, PMCID: PMC9587275, DOI: 10.1016/j.ebiom.2022.104304.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsidiopathic pulmonary fibrosisnon-human primatespulmonary fibrosisanimal modelspro-fibrotic genesanti-fibrotic efficacymiR-29 mimicshuman peripheral bloodmiR-29b levelshuman lung fibroblastsIPF patientsIPF diagnosisperipheral bloodreduced fibrosisadverse findingspotential therapylung slicesTGF-β1relevant doseslung fibroblastsNIH-NHLBIfibrosistherapycollagen productionprofibrotic gene programIntegrated Single-Cell Atlas of Endothelial Cells of the Human Lung
Schupp JC, Adams TS, Cosme C, Raredon MSB, Yuan Y, Omote N, Poli S, Chioccioli M, Rose KA, Manning EP, Sauler M, DeIuliis G, Ahangari F, Neumark N, Habermann AC, Gutierrez AJ, Bui LT, Lafyatis R, Pierce RW, Meyer KB, Nawijn MC, Teichmann SA, Banovich NE, Kropski JA, Niklason LE, Pe’er D, Yan X, Homer RJ, Rosas IO, Kaminski N. Integrated Single-Cell Atlas of Endothelial Cells of the Human Lung. Circulation 2021, 144: 286-302. PMID: 34030460, PMCID: PMC8300155, DOI: 10.1161/circulationaha.120.052318.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsdifferential expression analysisprimary lung endothelial cellslung endothelial cellscell typesmarker genesexpression analysissingle-cell RNA sequencing datacross-species analysisvenous endothelial cellsendothelial marker genessingle-cell atlasmarker gene setsRNA sequencing dataendothelial cellssubsequent differential expression analysisdifferent lung cell typesresident cell typeslung cell typescellular diversityendothelial cell typescapillary endothelial cellshuman lung endothelial cellsphenotypic diversityendothelial diversityindistinguishable populationsThyroid hormone inhibits lung fibrosis in mice by improving epithelial mitochondrial function
Yu G, Tzouvelekis A, Wang R, Herazo-Maya JD, Ibarra GH, Srivastava A, de Castro JPW, DeIuliis G, Ahangari F, Woolard T, Aurelien N, Arrojo e Drigo R, Gan Y, Graham M, Liu X, Homer RJ, Scanlan TS, Mannam P, Lee PJ, Herzog EL, Bianco AC, Kaminski N. Thyroid hormone inhibits lung fibrosis in mice by improving epithelial mitochondrial function. Nature Medicine 2017, 24: 39-49. PMID: 29200204, PMCID: PMC5760280, DOI: 10.1038/nm.4447.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsmicroRNA-33 deficiency in macrophages enhances autophagy, improves mitochondrial homeostasis, and protects against lung fibrosis
Ahangari F, Price N, Malik S, Chioccioli M, Bärnthaler T, Adams T, Kim J, Pradeep S, Ding S, Cosme C, Rose K, McDonough J, Aurelien N, Ibarra G, Omote N, Schupp J, DeIuliis G, Nunez J, Sharma L, Ryu C, Dela Cruz C, Liu X, Prasse A, Rosas I, Bahal R, Fernandez-Hernando C, Kaminski N. microRNA-33 deficiency in macrophages enhances autophagy, improves mitochondrial homeostasis, and protects against lung fibrosis. JCI Insight 2023, 8: e158100. PMID: 36626225, PMCID: PMC9977502, DOI: 10.1172/jci.insight.158100.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsidiopathic pulmonary fibrosispulmonary fibrosismiR-33miR-33 levelsspecific genetic ablationbronchoalveolar lavage cellsnovel therapeutic approachesmitochondrial homeostasisfatty acid metabolismmacrophages protectsbleomycin injurylavage cellslung fibrosishealthy controlsinflammatory responsetherapeutic approachesimmunometabolic responsescholesterol effluxfibrosisfatal diseasepharmacological inhibitionsterol regulatory element-binding protein (SREBP) genesgenetic ablationmacrophagesex vivo mouseSingle-cell RNA-seq reveals ectopic and aberrant lung-resident cell populations in idiopathic pulmonary fibrosis
Adams TS, Schupp JC, Poli S, Ayaub EA, Neumark N, Ahangari F, Chu SG, Raby BA, DeIuliis G, Januszyk M, Duan Q, Arnett HA, Siddiqui A, Washko GR, Homer R, Yan X, Rosas IO, Kaminski N. Single-cell RNA-seq reveals ectopic and aberrant lung-resident cell populations in idiopathic pulmonary fibrosis. Science Advances 2020, 6: eaba1983. PMID: 32832599, PMCID: PMC7439502, DOI: 10.1126/sciadv.aba1983.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsidiopathic pulmonary fibrosisvascular endothelial cellsIPF lungspulmonary fibrosischronic obstructive pulmonary disease (COPD) lungsfatal interstitial lung diseaseendothelial cellsinterstitial lung diseasecell populationsIPF myofibroblastsmyofibroblast focinonsmoker controlslung diseaseCOPD lungsbasaloid cellssingle-cell atlasinvasive fibroblastsmacrophage populationslungstromal cellsepithelial cellsfibrosiscellular populationsdevelopmental markerssingle-cell RNA-seqSingle-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis.
Zhao A, Unterman A, Abu Hussein N, Sharma P, Nikola F, Flint J, Yan X, Adams T, Justet A, Sumida T, Zhao J, Schupp J, Raredon M, Ahangari F, Deluliis G, Zhang Y, Buendia-Roldan I, Adegunsoye A, Sperling A, Prasse A, Ryu C, Herzog E, Selman M, Pardo A, Kaminski N. Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis. American Journal Of Respiratory And Critical Care Medicine 2024, 210: 1252-1266. PMID: 38924775, PMCID: PMC11568434, DOI: 10.1164/rccm.202401-0078oc.Peer-Reviewed Original ResearchCitationsAltmetricConceptsfibrotic hypersensitivity pneumonitisidiopathic pulmonary fibrosisperipheral blood mononuclear cellsbronchoalveolar lavage cellsblood mononuclear cellsclassical monocyteshypersensitivity pneumonitispulmonary fibrosisT cellsimmune perturbationslavage cellsmononuclear cellsCD8+ T cellscytotoxic T cellsinterstitial lung diseasehypersensitivity pneumonitis patientscytotoxic CD4immune aberrationspneumonic patientspneumonitislung diseasehealthy controlsimmune mechanismspatient cellssingle-cell transcriptomicsGene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans
Zuo F, Kaminski N, Eugui E, Allard J, Yakhini Z, Ben-Dor A, Lollini L, Morris D, Kim Y, DeLustro B, Sheppard D, Pardo A, Selman M, Heller RA. Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans. Proceedings Of The National Academy Of Sciences Of The United States Of America 2002, 99: 6292-6297. PMID: 11983918, PMCID: PMC122942, DOI: 10.1073/pnas.092134099.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptspulmonary fibrosisfibrotic lungshuman pulmonary fibrosispotential therapeutic targetgene expression analysisclinical diseasesmooth muscleknockout micetherapeutic targetfibrosishuman tissue samplesuntreatable grouplungtissue samplesmolecular pathwaysglobal gene expression analysisextracellular matrix formationmiceexpression analysismatrilysinmolecular mechanismskey regulatorgene expression patternsexpression patternsoligonucleotide microarraysMMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis
Rosas IO, Richards TJ, Konishi K, Zhang Y, Gibson K, Lokshin AE, Lindell KO, Cisneros J, MacDonald SD, Pardo A, Sciurba F, Dauber J, Selman M, Gochuico BR, Kaminski N. MMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis. PLOS Medicine 2008, 5: e93. PMID: 18447576, PMCID: PMC2346504, DOI: 10.1371/journal.pmed.0050093.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsidiopathic pulmonary fibrosisinterstitial lung diseasesubclinical interstitial lung diseasepulmonary fibrosislung diseaseIPF patientschronic progressive fibrotic lung diseasecontrol individualsasymptomatic interstitial lung diseaseprogressive fibrotic lung diseasechronic obstructive pulmonary diseasepotential peripheral blood biomarkerchronic hypersensitivity pneumonitisperipheral blood biomarkerschronic lung diseaseobstructive pulmonary diseasefibrotic lung diseasebronchoalveolar lavage fluidindependent validation cohortfamilial pulmonary fibrosisprotein signaturespulmonary diseasesubstantial morbidityhypersensitivity pneumonitislavage fluidInhibition and Role of let-7d in Idiopathic Pulmonary Fibrosis
Pandit KV, Corcoran D, Yousef H, Yarlagadda M, Tzouvelekis A, Gibson KF, Konishi K, Yousem SA, Singh M, Handley D, Richards T, Selman M, Watkins SC, Pardo A, Ben-Yehudah A, Bouros D, Eickelberg O, Ray P, Benos PV, Kaminski N. Inhibition and Role of let-7d in Idiopathic Pulmonary Fibrosis. American Journal Of Respiratory And Critical Care Medicine 2010, 182: 220-229. PMID: 20395557, PMCID: PMC2913236, DOI: 10.1164/rccm.200911-1698oc.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsMeSH KeywordsActinsAnimalsCadherinsCells, CulturedDown-RegulationEpithelial CellsHMGA2 ProteinHumansIdiopathic Pulmonary FibrosisIn Situ HybridizationLungMiceMice, Inbred C57BLMicroRNAsPolymerase Chain ReactionPulmonary AlveoliS100 Calcium-Binding Protein A4S100 ProteinsSmad3 ProteinTransforming Growth Factor betaVimentinConceptsidiopathic pulmonary fibrosisreal-time polymerase chain reactionquantitative real-time polymerase chain reactionalveolar epithelial cellsIPF lungspulmonary fibrosispolymerase chain reactionlet-7depithelial cellslethal fibrotic lung diseasealpha-smooth muscle actinalveolar septal thickeningmesenchymal markers N-cadherinfibrotic lung diseasechain reactionlet-7d expressionseptal thickeningpulmonary functionlung diseaselung fibrosisepithelial cell lineintratracheal administrationIPF tissueprofibrotic effectsclinical trialsSingle-cell atlas of human lung aging identifies cell type dyssynchrony and increased transcriptional entropy
De Man R, McDonough J, Adams T, Nikola F, Rangel R, Anderson S, Manning E, Cala Garcia J, Moss B, Waich A, Poli F, Cardenas R, Coarfa C, Song Q, Bar-Joseph Z, Vanaudenaerde B, Wuyts W, Niklason L, Raredon M, Yan X, Rosas I, Kaminski N. Single-cell atlas of human lung aging identifies cell type dyssynchrony and increased transcriptional entropy. Nature Communications 2026, 17: 2095. PMID: 41571679, PMCID: PMC12953888, DOI: 10.1038/s41467-026-68810-9.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsgenomic landscapelung agesingle-cell atlasalveolar epithelialindependent predictorsanalysis of somatic mutationssingle-cell datasingle-cell RNA sequencingendothelial cellsloss of differentiationalveolar epithelial cellsRNA sequencingtranscriptional changescell-typeendothelial cell typessomatic mutationsmutational burdenAT2 cellslung diseasecell typesage-related changesepithelial cellsrisk factorssenescence signatureEpithelial
Academic Achievements & Community Involvement
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Featured
honor Trudeau Honorary Lecture
04/26/2026National Award New York State Thoracic SocietyDetailsUnited Stateshonor Elected Member, Connecticut Academy of Science and Engineering (CASE)
06/25/2025Regional AwardConnecticut Academy of Science and Engineering (CASE)DetailsUnited Stateshonor J. Burns Amberson Honorary Award Lecture
05/15/2022International AwardAmerican Thoracic SocietyDetailsUnited Stateshonor Gold Medal for Interstitial Lung Disease
09/03/2016International AwardEuropean Respiratory SocietyDetailsUnited Kingdomhonor Helmholtz International Fellow Award
06/27/2013International AwardHelmholtz InstituteDetailsUnited States
Activities
activity American Thoracic Society
2018 - PresentProfessional OrganizationsFellowactivity American Society for the Advancement of Science
1999 - PresentProfessional OrganizationsMemberactivity Association of American Physicians
2015 - PresentProfessional OrganizationsMemberactivity InterUrban Clinical Club
2015 - PresentProfessional OrganizationsMemberactivity European Respiratory Society
2016 - PresentProfessional OrganizationsFellow
Honors
honor Morgagni Award for scientific research and commitment to promoting knowledge through logic and the scientific method."
10/22/2024International AwardMorgagni Pulmonary Diseases AssociationDetailsItalyhonor Blavatnic Fund Innovation Award
04/09/2019Yale School of Medicine AwardDetailsUnited Stateshonor Andy Tager Excellence in Mentorship Award
05/14/2018International AwardThe American Thoracic Society Respiratory Cell and Molecular Biology AssemblyDetailsUnited Stateshonor Fellow
05/14/2018National AwardAmerican Thoracic SocietyDetailsUnited Stateshonor Fellow
09/03/2016International AwardEuropean Respiratory SocietyDetailsUnited Kingdom
Clinical Care
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Overview
Naftali Kaminski, MD, chief of Yale Medicine Pulmonary, Critical Care and Sleep Medicine, is a leader in improving the understanding and treatment of chronic lung diseases. He has a particular interest in idiopathic pulmonary fibrosis, a disease characterized by progressive scarring of the lungs, and in chronic obstructive pulmonary disease and asthma.
Dr. Kaminski leads the Kaminski Lab at Yale School of Medicine, where researchers apply cutting-edge technologies that measure changes in the sequence, expression or regulation of all the genes in the human genome in efforts to learn more about the roles of genome networks and biomarkers in chronic lung disease.
“Pulmonary fibrosis was an understudied and poorly understood disease, with high mortality and morbidity,” says Dr. Kaminiski, who is a professor of medicine (pulmonary) at Yale School of Medicine “I thought that by shifting the focus to human
relevant pathways and mechanisms we can have an impact, and we have.”
Clinical Specialties
Fact Sheets
Interstitial Lung Disease (ILD)
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News & Links
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Media
- Dr. Kaminski Receiving the Helmholtz International Award from Dr. Eickelberg in Munich, June 2013
How Lungs Age
Scientists created a cellular atlas of the lungs to pinpoint cells especially vulnerable to aging. They could be targeted to prevent acute and chronic lung diseases.
News
- July 23, 2026
Master of Health Science Welcomes New Leadership for Clinical Investigation Program
- July 20, 2026
YSM Joins International Team to Develop AI for Precision Medicine
- June 11, 2026
How Do Financial Conflicts of Interest Influence Medical Prescribing Practices?
- May 27, 2026
Connecting the Dots Across Yale School of Medicine
Related Links
- Dr. Kaminski answers to the question "What Excites you Most about the Future?"
- Dr. Kaminski is joining Yale faculty as Chief of Pulmonary, Critical Care and Sleep Medicine
- IPF Awareness at Yale PCCSM 2014
- Jerusalem Post: Israeli becomes top world expert on lung disease
- Role of Biomarkers in Diagnosis and Treatment of IPF
- Dr. Kaminski speaking about advocacy for ending sexual harassment and gender inequality
- Dr. Kaminski speaking about Cell-based Precision Medicine Approaches to PF in the PF Summit 2020
- Introduction of the Kaminski Lab to computational Students
- Dr. Kaminski speaks about the role of men in fighting gender inequality and sexual harassment at the Branford Forum
- Dr. Kaminski's Amberson Award Talk
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Contacts
Pulmonary, Critical Care & Sleep Medicine
300 Cedar Street, TAC-441 South, PO Box 208057
New Haven, CT 06520-8057
United States
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The Anlyan Center
Academic Office
300 Cedar Street, Ste S441D
New Haven, CT 06519
Appointments
203.737.4612Patient Care Locations
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