D. Labuda

D. Labuda, M. Krajinovic, D. Sinnett, 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia.

D. Labuda, M. Krajinovic, D. Sinnett, 2004, Blood.

Role of DNA mismatch repair genetic polymorphisms in the risk of childhood acute lymphoblastic leukaemia

D. Labuda, M. Krajinovic, D. Sinnett, 2003, British journal of haematology.

Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms.

D. Labuda, M. Krajinovic, D. Sinnett, 1999, Epidemiology.

Childhood Acute Lymphoblastic Leukemia Associated with Parental Alcohol Consumption and Polymorphisms of Carcinogen-Metabolizing Genes

D. Labuda, M. Krajinovic, D. Sinnett, 2002, Epidemiology.

Alu-PCR combined with non-Alu primers reveals multiple polymorphic loci

D. Labuda, M. Jarnik, S. Melançon, 1995, Mammalian Genome.

Dynamic allele-specific oligonucleotide hybridization on solid support.

D. Labuda, S. Bourgeois, Stephane Bourgeois, 2004, Analytical biochemistry.

lymphoblastic leukemia genetic polymorphisms and susceptibility to childhood acute MTHFR

D. Labuda, Rajiv Kumar, B. Burwinkel, 2011 .

Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy

D. Labuda, J. Bouchard, B. Brais, 2005, Annals of neurology.

Neutral polymorphisms in the deletion-prone regions of the dystrophin gene.

D. Labuda, E. Ziętkiewicz, N. Akalın, 1995, Human heredity.

Lipid processing and lipoprotein synthesis by the developing human fetal colon.

D. Labuda, E. Levy, T. Nguyen, 1996, The American journal of physiology.

Susceptibility to Childhood Acute Lymphoblastic Leukemia : Influence of CYP 1 A 1 , CYP 2 D 6 , GSTM 1 , and GSTT 1 Genetic Polymorphisms

D. Labuda, M. Krajinovic, D. Sinnett, 1999 .

Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages

D. Reich, C. Lalueza-Fox, D. Labuda, 2017, Proceedings of the Royal Society B: Biological Sciences.

Phylogenetic analysis of a reported complementary DNA sequence.

D. Labuda, W. Makałowski, E. Ziętkiewicz, 1994, Science.

Parental genotypes in the risk of a complex disease.

D. Labuda, M. Krajinovic, D. Sinnett, 2002, American journal of human genetics.

PRENATAL DIAGNOSIS USING DNA PROBES IN TWINS AT RISK FOR DUCHENNE MUSCULAR DYSTROPHY

D. Labuda, D. Sinnett, L. Lavergne, 1986, The Lancet.

Small cytoplasmic Ro RNA pseudogene and an Alu repeat in the human alpha-1 globin gene.

T. Smith, J. Jurka, D. Labuda, 1988, Nucleic acids research.

Complementary DNA for 12-kilodalton B cell growth factor: misassigned.

D. Labuda, W. Makałowski, E. Ziętkiewicz, 1996, Science.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm

Steven J. M. Jones, D. Labuda, H. Dietz, 2014, Nature Genetics.

Genomic loci susceptible to replication errors in cancer cells.

D. Labuda, M. Krajinovic, D. Sinnett, 1998, British Journal of Cancer.

Deep Human Genealogies Reveal a Selective Advantage to Be on an Expanding Wave Front

Laurent Excoffier, Claudia Moreau, Damian Labuda, 2011, Science.

Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes

D. Labuda, M. Krajinovic, D. Sinnett, 2003, Journal of Human Genetics.

An in vitro selection scheme for oligonucleotide probes to discriminate between closely related DNA sequences

I. Brukner, D. Labuda, M. Krajinovic, 2007, Nucleic acids research.

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution.

D. Labuda, K. Schappert, A. Duncan, 1994, Genomics.

Chromosomal assignment of loci susceptible to replication errors by radiation hybrid mapping.

D. Labuda, M. Krajinovic, D. Sinnett, 1998, Mutation research.

Human estrogen receptor beta 548 is not a common variant in three distinct populations.

D. Labuda, K. Hemminki, K. Dahlman-Wright, 2003, Endocrinology.

Phi29-based amplification of small genomes.

I. Brukner, D. Labuda, M. Krajinovic, 2006, Analytical biochemistry.

Phi 29-based ampli W cation of small genomes

I. Brukner, D. Labuda, M. Krajinovic, 2006 .

Childhood Acute Lymphoblastic Leukemia: Genetic Determinants of Susceptibility and Disease Outcome

D. Labuda, M. Krajinovic, D. Sinnett, 2001, Reviews on environmental health.

Codon-induced tRNA association: quantitative analysis by sedimentation equilibrium

D. Labuda, D. Poerschke, 1982 .

Magnesium ion inner sphere complex in the anticodon loop of phenylalanine transfer ribonucleic acid.

D. Labuda, D. Poerschke, D. Pörschke, 1982, Biochemistry.

The three conformations of the anticodon loop of yeast tRNA(Phe).

D. Labuda, G. Striker, M. C. Vega-Martin, 1989, Journal of biomolecular structure & dynamics.

Apparent cooperativity of cation binding to protonated transfer RNA measured by quantitation of released protons.

D. Labuda, J. Augustyniak, P. J. de Varebeke, 1978, Biochemical and biophysical research communications.

Dependence of tRNA structure in solution upon ionic condition of the solvent. Fluorescence studies of monovalent cation binding to tRNAPhe from barley embryos.

D. Labuda, J. Augustyniak, 1977, European journal of biochemistry.

Dependence of tRNA structure in solution upon ionic condition of the solvent. Fluorescence studies of Mg2+ binding to tRNAPhe from barley embryos.

D. Labuda, T. Haertlé, J. Augustyniak, 1977, European journal of biochemistry.

Effect of Na+ ion concentration on tRNA conformation in solution studied by laser Raman spectroscopy

D. Labuda, A. Patkowski, A. Dobek, 1975 .

Admixture dynamics in Hispanics: a shift in the nuclear genetic ancestry of a South American population isolate.

Andrés Ruiz-Linares, Damian Labuda, Jorge Ospina, 2006, Proceedings of the National Academy of Sciences of the United States of America.

The Genomic History of Southeastern Europe

Ivor Karavanić, Swapan Mallick, Thomas Higham, 2017, Nature.

Tracing genetic history of modern humans using X-chromosome lineages

Scott M. Williams, J. Jurka, D. Labuda, 2007, Human Genetics.

Reconciling migration models to the Americas with the variation of North American native mitogenomes

R. J. Herrera, D. Labuda, A. Torroni, 2013, Proceedings of the National Academy of Sciences.

A protocol for the in vitro selection of specific oligonucleotide probes for high-resolution DNA typing

Damian Labuda, I. Brukner, D. Labuda, 2007, Nature Protocols.

Aminoacids and the anticodon: anticodon interaction: a test of the stereochemical hypothesis?

D. Labuda, H. Grosjean, 1981, Biochimie.

Sequence conservation in Alu evolution.

D. Labuda, G. Striker, 1989, Nucleic acids research.

Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification.

D. Labuda, E. Ziętkiewicz, A. Rafalski, 1994, Genomics.

Use of γ irradiation to eliminate DNA contamination for PCR

D. Labuda, D. Sinnett, J. Deragon, 1990 .

Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy.

S. Tavaré, M. Batzer, D. Labuda, 1999, Genetics.

Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia

D. Labuda, M. Krajinovic, D. Sinnett, 2002, International journal of cancer.

Mechanism of codon recognition by transfer RNA studied with oligonucleotides larger than triplets.

D. Labuda, G. Striker, H. Grosjean, 1985, Nucleic acids research.

Codon:anticodon and anticodon:anticodon interaction: evaluation of equilibrium and kinetic parameters of complexes involving a g:u wobble.

D. Labuda, G. Striker, H. Grosjean, 1982, Biochimica et biophysica acta.

Multistep mechanism of codon recognition by transfer ribonucleic acid.

D. Labuda, D. Poerschke, D. Pörschke, 1980, Biochemistry.

Alu RNA transcripts in human embryonal carcinoma cells. Model of post-transcriptional selection of master sequences.

D. Labuda, D. Sinnett, C. Richer, 1992, Journal of molecular biology.

Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity.

David Modiano, Damian Labuda, M. Batzer, 2003, American journal of human genetics.

Genetic Structure of the Ancestral Population of Modern Humans

S. Tishkoff, K. Kidd, M. Stoneking, 1998, Journal of Molecular Evolution.

Nuclear DNA diversity in worldwide distributed human populations.

S. Tishkoff, K. Kidd, M. Stoneking, 1997, Gene.

Codon-induced transfer RNA association. A property of transfer RNA involved in its adaptor function?

D. Labuda, D. Poerschke, D. Pörschke, 1983, Journal of molecular biology.

Alumorphs--human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers.

D. Labuda, D. Sinnett, J. Deragon, 1990, Genomics.

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

J. Weissenbach, D. Labuda, F. Glorieux, 1996, American journal of human genetics.

Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era

Jerzy Jurka, Damian Labuda, Ewa Zietkiewicz, 1995, Nucleic Acids Res..

Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units.

D. Labuda, D. Sinnett, C. Richer, 1991, The Journal of biological chemistry.

Is selection responsible for the low level of variation in the last intron of the ZFY locus?

D. Labuda, E. Ziętkiewicz, J. Jaruzelska, 1999, Molecular biology and evolution.

A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

D. Labuda, G. Rouleau, F. Hamdan, 2015, Clinical genetics.

X-Linked MTMR8 Diversity and Evolutionary History of Sub-Saharan Populations

Scott M. Williams, D. Labuda, C. Moreau, 2013, PloS one.

Contrasting Patterns of Nuclear and mtDNA Diversity in Native American Populations

L. Excoffier, Sijia Wang, N. Ray, 2010, Annals of human genetics.

CORE-SINEs: eukaryotic short interspersed retroposing elements with common sequence motifs.

D. Labuda, N. Gilbert, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Allelic losses and DNA methylation at DNA mismatch repair loci in sporadic colorectal cancer.

D. Labuda, D. Sinnett, N. Benachenhou, 1998, Carcinogenesis.

Genomic and genealogical investigation of the French Canadian founder population structure

D. Labuda, D. Sinnett, C. Laprise, 2011, Human Genetics.

Historical human remains identification through maternal and paternal genetic signatures in a founder population with extensive genealogical record.

C. Lalueza-Fox, D. Labuda, C. Laprise, 2020, American journal of physical anthropology.

Female-to-male breeding ratio in modern humans-an analysis based on historical recombinations.

D. Labuda, M. Roy-Gagnon, J. Lefebvre, 2010, American journal of human genetics.

An X-linked haplotype of Neandertal origin is present among all non-African populations.

R. Scott, D. Labuda, C. Moreau, 2011, Molecular biology and evolution.

Genetic heterogeneity in regional populations of Quebec--parental lineages in the Gaspe Peninsula.

P. de Knijff, D. Labuda, D. Sinnett, 2009, American journal of physical anthropology.

Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia.

Daniel Sinnett, Jasmine Healy, Damian Labuda, 2007, Blood.

When Genetics and Genealogies Tell Different Stories—Maternal Lineages in Gaspesia

D. Labuda, H. Vézina, C. Moreau, 2010, Annals of human genetics.

Assessing DNA sequence variations in human ESTs in a phylogenetic context using high-density oligonucleotide arrays.

Damian Labuda, Thomas J Hudson, Jean-Philippe Laviolette, 2002, Genomics.

Mother’s curse neutralizes natural selection against a human genetic disease over three centuries

A. Cohen, D. Labuda, B. Brais, 2017, Nature Ecology & Evolution.

Mechanism of codon recognition by transfer RNA and codon-induced tRNA association.

D. Labuda, G. Striker, D. Porschke, 1984, Journal of molecular biology.

Susceptibility to childhood acute lymphoblastic leukemia: influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 genetic polymorphisms.

D. Labuda, M. Krajinovic, D. Sinnett, 1999, Blood.

A young Alu subfamily amplified independently in human and African great apes lineages.

J. Jurka, D. Labuda, W. Makałowski, 1994, Nucleic acids research.

Evolution of mouse B1 repeats: 7SL RNA folding pattern conserved

D. Labuda, G. Striker, D. Sinnett, 1991, Journal of Molecular Evolution.

Phylogenetic affinities of tarsier in the context of primate Alu repeats.

D. Labuda, E. Ziętkiewicz, C. Richer, 1999, Molecular phylogenetics and evolution.

Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes.

Daniel Sinnett, Damian Labuda, Thomas J Hudson, 2006, Genomics.

Standardized nomenclature for Alu repeats

Carl W. Schmid, Damian Labuda, Emile Zuckerkandl, 2004, Journal of Molecular Evolution.

Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families

D. Labuda, S. Tavtigian, J. Simard, 2006, BMC Cancer.

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

X. Estivill, P. Talmud, D. Labuda, 2007, Journal of Medical Genetics.

Genotype-Based Test in Mapping Cis-Regulatory Variants from Allele-Specific Expression Data

E. Dermitzakis, S. Montgomery, D. Labuda, 2012, PloS one.

DNA variants in the dihydrofolate reductase gene and outcome in childhood ALL.

D. Labuda, M. Krajinovic, D. Sinnett, 2008, Blood.

Evolution of secondary structure in the family of 7SL-like RNAs

D. Labuda, Ewa Zitkiewicz, 1994, Journal of Molecular Evolution.

Functional impact of sequence variation in the promoter region of TGFB1

D. Labuda, D. Sinnett, P. Beaulieu, 2009, International journal of cancer.

Ethiopia: between Sub-Saharan Africa and western Eurasia.

D. Labuda, J. Bertranpetit, C. Moreau, 2005, Annals of human genetics.

The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim.

D. Labuda, M. Labuda, E. Ziętkiewicz, 1997, American journal of human genetics.

Patterns of variation in DNA segments upstream of transcription start sites

T. Hudson, D. Labuda, T. Pastinen, 2007, Human mutation.

Mutations in TMEM231 cause Joubert syndrome in French Canadians

D. Labuda, E. Lemyre, G. Rouleau, 2012, Journal of Medical Genetics.

Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.

D. Labuda, G. Rouleau, K. Boycott, 2012, American journal of human genetics.

Subcellular proteomics of cell differentiation: Quantitative analysis of the plasma membrane proteome of Caco‐2 cells

D. Labuda, A. Pshezhetsky, E. Levy, 2007, Proteomics.

Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the evolutionary history of the disease

D. Labuda, A. Pshezhetsky, R. Giugliani, 2019, Human mutation.

Genetic Susceptibility to Childhood Acute Lymphoblastic Leukemia

D. Labuda, M. Krajinovic, D. Sinnett, 2000, Leukemia & lymphoma.

Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity

F. Salzano, S. Chanock, A. Sajantila, 2007, The Pharmacogenomics Journal.

Mother’s curse neutralizes natural selection against a human genetic disease over three centuries

A. Cohen, D. Labuda, B. Brais, 2017, Nature Ecology & Evolution.

Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec

T. Hudson, B. Toupance, D. Labuda, 2005, Human Genetics.

GENLIB: an R package for the analysis of genealogical data

D. Labuda, H. Vézina, C. Moreau, 2015, BMC Bioinformatics.

Native American Admixture in the Quebec Founder Population

A. Ruiz-Linares, D. Labuda, H. Vézina, 2013, PloS one.

Reverse transcriptase activity from human embryonal carcinoma cells NTera2D1.

D. Labuda, D. Sinnett, J. Deragon, 1990, The EMBO journal.

Genetic susceptibility to breast cancer in French‐Canadians: Role of carcinogen‐metabolizing enzymes and gene–environment interactions

A. LaCroix, D. Labuda, M. Krajinovic, 2001, International journal of cancer.

Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population

Claudia Moreau, Damian Labuda, Hélène Vézina, 2013, European Journal of Human Genetics.

Fraction of Informative Recombinations: A Heuristic Approach to Analyze Recombination Rates

D. Labuda, J. Lefebvre, 2008, Genetics.

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

C. Fallet-Bianco, D. Labuda, H. Mandel, 2015, American journal of human genetics.

Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction.

D. Labuda, M. Krajinovic, D. Sinnett, 1996, Cancer research.

Genetic diversity patterns at the human clock gene period 2 are suggestive of population-specific positive selection

D. Labuda, A. Torroni, R. Scozzari, 2008, European Journal of Human Genetics.

Challenges Identifying Genetic Determinants of Pediatric Cancers – the Childhood Leukemia Experience

D. Labuda, M. Krajinovic, D. Sinnett, 2005, Familial Cancer.

International Congress on Hormonal Steroids and Hormones and Cancer Prostate cancer susceptibility genes: lessons learned and challenges posed

D. Labuda, S. Tavtigian, M. Dumont, 2003 .

Brief communication: patterns of linkage disequilibrium and haplotype diversity at Xq13 in six Native American populations.

Sijia Wang, G. Bedoya, A. Ruiz-Linares, 2009, American journal of physical anthropology.

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families.

D. Labuda, L. Simard, B. Lemieux, 1992, Genomics.

Haplotype allelic classes for detecting ongoing positive selection

Philippe Nadeau, Julie Hussin, Jean-François Lefebvre, 2010, BMC Bioinformatics.

Genetic Structure of First Nation Communities in the Pacific Northwest

Cris E. Hughes, D. Labuda, R. Malhi, 2016, Human Biology.

Relationship between 2'-hydroxyls and magnesium binding in the hammerhead RNA domain: a model for ribozyme catalysis.

D. Labuda, R. Cedergren, N. Usman, 1991, Biochemistry.

Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec

D. Labuda, L. Simard, M. Vanasse, 1992, Human Genetics.

Genetic variation in the enigmatic Altaian Kazakhs of South-Central Russia: insights into Turkic population history.

O. Gokcumen, D. Labuda, A. Pai, 2008, American journal of physical anthropology.

Rapid detection of CYP1A1, CYP2D6, and NAT variants by multiplex polymerase chain reaction and allele-specific oligonucleotide assay.

D. Labuda, M. Krajinovic, D. Sinnett, 1999, Analytical biochemistry.

Y-chromosome evidence for differing ancient demographic histories in the Americas.

G. Bedoya, K. Hill, A. Hurtado, 2003, American journal of human genetics.

The effective family size of immigrant founders predicts their long-term demographic outcome: From Québec settlers to their 20th-century descendants

D. Labuda, H. Vézina, E. Milot, 2021, bioRxiv.

Self-priming arrest by modified random oligonucleotides facilitates the quality control of whole genome amplification.

I. Brukner, D. Labuda, M. Krajinovic, 2005, Analytical biochemistry.

Polymorphisms within a polymorphism: SNPs in and around a polymorphic Alu insertion in intron 44 of the human dystrophin gene

M. Batzer, D. Labuda, V. Yotova, 2004, Journal of Human Genetics.

Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer

D. Labuda, D. Sinnett, N. Benachenhou, 1999, British Journal of Cancer.

Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.

D. Labuda, G. Lettre, J. Tardif, 2014, The Canadian journal of cardiology.

In vitro evolution of RNA aptamers recognizing carcinogenic aromatic amines.

Damian Labuda, Wolfgang Pfau, A. Montpetit, 2004, Biochemical and biophysical research communications.

The catalytic function of hormone-sensitive lipase is essential for fertility in male mice.

D. Labuda, B. Leavitt, G. Mitchell, 2014, Endocrinology.

Genetic diversity patterns in the SR-BI/II locus can be explained by a recent selective sweep.

D. Labuda, E. Levy, D. Sinnett, 2004, Molecular biology and evolution.

Direct analysis of amniotic fluid cells by multiplex PCR provides rapid prenatal diagnosis for Duchenne muscular dystrophy.

D. Labuda, L. Simard, F. Gingras, 1991, Nucleic acids research.

Admixed ancestry and stratification of Quebec regional populations.

D. Labuda, H. Vézina, M. Roy-Gagnon, 2011, American journal of physical anthropology.

Use of gamma irradiation to eliminate DNA contamination for PCR.

D. Labuda, D. Sinnett, J. Deragon, 1990, Nucleic acids research.

Valyl tRNA's of Anacystis nidulans

D. Labuda, A. Gozdzicka-Jozefiak, G. Borbély, 1975 .

Newly‐isolated HPV97, related to HPV18 and 45 is frequently detected in HIV‐positive men from the montreal area

I. Brukner, D. Labuda, M. Krajinovic, 2007, International Journal of Cancer.

Analyses of bulky DNA adduct levels in human breast tissue and genetic polymorphisms of cytochromes P450 (CYPs), myeloperoxidase (MPO), quinone oxidoreductase (NQO1), and glutathione S-transferases (GSTs).

D. Labuda, M. Krajinovic, D. Sinnett, 2002, Mutation research.

Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria

C. Fallet-Bianco, D. Labuda, E. Brustein, 2015, Journal of Medical Genetics.

Concordance Between Reported Ethnic Origins and Ancestral Origins of Gaspé Peninsula Residents

D. Labuda, H. Vézina, M. Tremblay, 2014 .

Hybridization assay performed at ambient temperature for typing high-risk human papillomaviruses.

I. Brukner, D. Labuda, M. Krajinovic, 2007, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts

D. Labuda, C. Moreau, E. Ziętkiewicz, 2004, European Journal of Human Genetics.

Characterization of the BclI polymorphism in the glucocorticoid receptor gene.

D. Labuda, M. Krajinovic, D. Sinnett, 2003, Clinical chemistry.

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR.

D. Labuda, F. Glorieux, D. Sinnett, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus

D. Labuda, D. Sinnett, C. Richer, 1992, Human Genetics.

Mosaic evolution of rodent B1 elements

D. Labuda, E. Ziętkiewicz, 2004, Journal of Molecular Evolution.

Light scattering by solutions of tRNA molecules oriented in D.C. magnetic field

D. Labuda, A. Patkowski, A. Dobek, 2007 .