J. Bertranpetit

D. Comas, J. Bertranpetit, M. Gardner, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A prevalent POLG CAG microsatellite length allele in humans and African great apes

A. Andrés, H. Jacobs, J. Bertranpetit, 2004, Mammalian Genome.

A Targeted Association Study of Immunity Genes and Networks Suggests Novel Associations with Placental Malaria Infection

M. Netea, C. Menéndez, J. Bertranpetit, 2011, PloS one.

Genome-Wide Pathway Analysis Identifies Genetic Pathways Associated with Psoriasis.

D. Absher, R. Myers, J. Gelpí, 2016, The Journal of investigative dermatology.

A variant in the gene FUT9 is associated with susceptibility to placental malaria infection.

C. Menéndez, J. Bertranpetit, M. Sikora, 2009, Human molecular genetics.

Recent human evolution has shaped geographical differences in susceptibility to disease

U. Marigorta, J. Bertranpetit, R. Faria, 2011, BMC Genomics.

Y-chromosome diversity in Bantu and Pygmy populations from Central Africa

D. Comas, J. Bertranpetit, E. Bosch, 2006 .

Allele frequencies for 20 microsatellites in a worldwide population survey.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human heredity.

Neuropathologic Findings in an Aged Albino Gorilla

J. Bertranpetit, I. Ferrer, A. Ferrer-Admetlla, 2008, Veterinary pathology.

Geographic population structure analysis of worldwide human populations infers their biogeographical origins

Ajay K. Royyuru, Michael Hammer, Laxmi Parida, 2014, Nature Communications.

Hunter-gatherer oral microbiomes are shaped by contact network structure

J. Gómez-Gardeñes, V. Latora, M. Greenacre, 2022, bioRxiv.

Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage

K. Kidd, A. Andrés, J. Bertranpetit, 2004, Human Genetics.

Influence of pathway topology and functional class on the molecular evolution of human metabolic genes

Kevin L. Keys, J. Bertranpetit, J. Peretó, 2018, bioRxiv.

Cerdanya: mountain valley, genetic highway.

J. Bertranpetit, H. Macbeth, M. Salvat, 1996, Annals of human biology.

Variation of the prion gene in chimpanzees and its implication for prion diseases

A. Andrés, J. Bertranpetit, F. Calafell, 2004, Neuroscience Letters.

Sequence variability of a human pseudogene.

A. Andrés, D. Comas, J. Bertranpetit, 2001, Genome research.

Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apes

A. Andrés, J. Bertranpetit, V. Volpini, 2003, Neuroscience Letters.

University of Birmingham From cheek swabs to consensus sequences

Nirav C. Merchant, Owings, R. J. Mitchell, 2014 .

HSP70-2 (HSPA1B) is Associated with Noncognitive Symptoms in Late-Onset Alzheimer's Disease

D. Comas, J. Bertranpetit, J. Clarimón, 2003, Journal of geriatric psychiatry and neurology.

HSP 702 ( HSPA 1 B ) Is Associated With Noncognitive Symptoms in Late-Onset Alzheimer ’ s Disease

D. Comas, J. Bertranpetit, J. Clarimón, 2003 .

Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder.

B. Gutiérrez, V. Vallès, R. Guillamat, 1997, The American journal of psychiatry.

Is There Selection for the Pace of Successive Inactivation of the arpAT Gene in Primates?

D. Torrents, J. Bertranpetit, F. Casals, 2008, Journal of Molecular Evolution.

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism.

C. Tyler-Smith, M. Hurles, M. Jobling, 1999, American journal of human genetics.

Mountains and genes: population history of the Pyrenees.

J. Bertranpetit, F. Calafell, 1994, Human biology.

Genetic markers in schizophrenia: ACP1, ESD, TF and GC polymorphisms.

L. Fañanás, J. Bertranpetit, P. Moral, 1990, Human heredity.

Reply to — Age of the ΔF508 cystic fibrosis mutation

X. Estivill, J. Bertranpetit, N. Morral, 1994, Nature Genetics.

Concise report A genome-wide association study identifies SLC8A3 as a susceptibility locus for ACPA-positive rheumatoid arthritis RHEUMATOLOGY

D. Absher, J. Gelpí, J. Bertranpetit, 2016 .

Dermatoglyphic a-b ridge count and risk for schizophrenia

R. Murray, J. Os, L. Fañanás, 1996, Schizophrenia Research.

Parental age in schizophrenia in a case-controlled study

L. Fañanás, J. Bertranpetit, 1993, British Journal of Psychiatry.

Y chromosome STR haplotypes in four populations from northwest Africa

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 2000, International Journal of Legal Medicine.

Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean.

C. Tyler-Smith, M. Jobling, Yali Xue, 2008, American journal of human genetics.

Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events

R. J. Herrera, C. Tyler-Smith, Yali Xue, 2008, American journal of human genetics.

Birth, marriage and death in illegitimacy: a study in northern Portugal

J. Bertranpetit, A. Abade, 1995, Journal of Biosocial Science.

Palaeogenetic evidence supports a dual model of Neolithic spreading into Europe

C. Lalueza-Fox, J. Bertranpetit, O. Lao, 2007, Proceedings of the Royal Society B: Biological Sciences.

Population Genetics of Y-Chromosome Short Tandem Repeats in Humans

Francesc Calafell, Jaume Bertranpetit, David Comas, 1997, Journal of Molecular Evolution.

A genetic reconstruction of the history of the population of the Iberian Peninsula

L. Cavalli-Sforza, J. Bertranpetit, L. L. Cavalli-Sforza, 1991, Annals of human genetics.

The Genetic History of the Iberian Peninsula: A Simulation

Francesc Calafell, Jaume Bertranpetit, J. Bertranpetit, 1993, Current Anthropology.

Human Population Dynamics: Cross-Disciplinary Perspectives: From genetic variation to population dynamics: insights into the biological understanding of humans

J. Bertranpetit, F. Calafell, 2002 .

An integrative evolution theory of histo-blood group ABO and related genes

N. Saitou, J. Bertranpetit, A. Blancher, 2014, Scientific Reports.

Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome‐Wide Association Study

D. Absher, R. Myers, J. Bertranpetit, 2016, Arthritis & rheumatology.

A natural history of FUT2 polymorphism in humans.

J. Bertranpetit, M. Sikora, F. Casals, 2009, Molecular biology and evolution.

Genomic Affinities of Two 7,000-Year-Old Iberian Hunter-Gatherers

Federico Sánchez-Quinto, C. Lalueza-Fox, M. Pybus, 2012, Current Biology.

Tracking down human contamination in ancient human teeth.

C. Lalueza-Fox, J. Bertranpetit, O. Lao, 2006, Molecular biology and evolution.

Neandertal evolutionary genetics: mitochondrial DNA data from the iberian peninsula.

C. Lalueza-Fox, M. de la Rasilla, A. Rosas, 2005, Molecular biology and evolution.

Evidence for a genetic discontinuity between Neandertals and 24,000-year-old anatomically modern Europeans

C. Lalueza-Fox, I. Dupanloup, J. Bertranpetit, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Paleogenomics in a Temperate Environment: Shotgun Sequencing from an Extinct Mediterranean Caprine

C. Lalueza-Fox, J. Bertranpetit, J. Castresana, 2009, PloS one.

A Melanocortin 1 Receptor Allele Suggests Varying Pigmentation Among Neanderthals

Jaume Bertranpetit, Antonio Rosas, Mark Stoneking, 2007, Science.

Genetic analysis of the skeletal remains attributed to Francesco Petrarca.

C. Lalueza-Fox, C. Capelli, J. Bertranpetit, 2007, Forensic science international.

Nuclear Gene Indicates Coat-Color Polymorphism in Mammoths

Jaume Bertranpetit, Eske Willerslev, Carles Lalueza-Fox, 2006, Science.

The Genetics of the Pre‐Roman Iberian Peninsula: A mtDNA Study of Ancient Iberians

C. Lalueza-Fox, D. Comas, J. Bertranpetit, 2005, Annals of human genetics.

Unravelling migrations in the steppe: mitochondrial DNA sequences from ancient Central Asians

C. Lalueza-Fox, J. Bertranpetit, D. Pettener, 2004, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Genetic characterization of the ABO blood group in Neandertals

Jaume Bertranpetit, Carles Lalueza-Fox, Elena Gigli, 2008, BMC Evolutionary Biology.

The origin of the major cystic fibrosis mutation (ΔF508) in European populations

X. Estivill, J. Kere, J. Bertranpetit, 1994, Nature Genetics.

On the association between chromosomal rearrangements and genic evolution in humans and chimpanzees

L. Armengol, T. Marquès-Bonet, M. Rocchi, 2007, Genome Biology.

Comparative Analysis of Alu Insertion Sequences in the APP 5′ FlankingRegion in Humans and Other Primates

A. Andrés, D. Comas, J. Bertranpetit, 2004, Journal of Molecular Evolution.

Alu insertion polymorphisms in the Balkans and the origins of the Aromuns

D. Comas, J. Bertranpetit, F. Calafell, 2004, Annals of human genetics.

High-resolution analysis of human Y-chromosome variation shows a sharp discontinuity and limited gene flow between northwestern Africa and the Iberian Peninsula.

P. Underhill, P. Oefner, D. Comas, 2001, American journal of human genetics.

Y chromosome sequence variation and the history of human populations

Li Jin, Jaume Bertranpetit, Alberto Piazza, 2000, Nature Genetics.

Genome, diversity, and origins: the Y chromosome as a storyteller.

J. Bertranpetit, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Reproductive rates in families of schizophrenic patients in a case‐control study

L. Fañanás, J. Bertranpetit, 1995, Acta psychiatrica Scandinavica.

Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans

Nirav C. Merchant, C. Tyler-Smith, J. Korlach, 2013, Nature Communications.

Selection in the Introgressed Regions of the Chimpanzee Genome

Martin Kuhlwilm, T. Marquès-Bonet, J. Bertranpetit, 2018, Genome biology and evolution.

Natural Selection in the Great Apes

A. Andrés, T. Marquès-Bonet, M. Pybus, 2016, Molecular biology and evolution.

Recombination gives a new insight in the effective population size and the history of the old world human populations.

Francesc Calafell, Laxmi Parida, Jaume Bertranpetit, 2012, Molecular biology and evolution.

Genetic variation in prehistoric Sardinia

C. Lalueza-Fox, J. Bertranpetit, G. Bertorelle, 2007, Human Genetics.

Mitochondrial DNA of an Iberian Neandertal suggests a population affinity with other European Neandertals

Francesc Calafell, Jaume Bertranpetit, Antonio García-Tabernero, 2006, Current Biology.

A highly divergent mtDNA sequence in a Neandertal individual from Italy

C. Lalueza-Fox, A. Manfredini, J. Bertranpetit, 2006, Current Biology.

P. Awadalla, D. Comas, Marta Melé, 2011, PloS one.

PopHuman: the human population genomics browser

Jaume Bertranpetit, Hafid Laayouni, Sònia Casillas, 2017, Nucleic Acids Res..

Sequences From First Settlers Reveal Rapid Evolution in Icelandic mtDNA Pool

K. Stefánsson, C. Lalueza-Fox, A. Baker, 2009, PLoS genetics.

Mitochondrial DNA from pre-Columbian Ciboneys from Cuba and the prehistoric colonization of the Caribbean.

C. Lalueza-Fox, J. Bertranpetit, F. Calafell, 2003, American journal of physical anthropology.

MtDNA from extinct Tainos and the peopling of the Caribbean

C. Lalueza-Fox, J. Bertranpetit, F. Calderon, 2001 .

Mitochondrial DNA from Myotragus balearicus, an extinct bovid from the Balearic Islands.

E. Hagelberg, C. Lalueza-Fox, J. Bertranpetit, 2000, The Journal of experimental zoology.

A tale of two islands: population history and mitochondrial DNA sequence variation of Bioko and São Tomé, Gulf of Guinea

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Annals of Human Genetics.

Heteroplasmy in the control region of human mitochondrial DNA.

S. Pääbo, D. Comas, J. Bertranpetit, 1995, Genome research.

Geographic patterns of mtDNA diversity in Europe.

J. Bertranpetit, G. Barbujani, F. Calafell, 2000, American journal of human genetics.

Neandertal genetics.

S. Pääbo, J. Bertranpetit, R. Hedges, 1997, Science.

Signatures of genetic variation in human microRNAs point to processes of positive selection related to population-specific disease risks

J. Bertranpetit, H. Laayouni, Y. Espinosa-Parrilla, 2021, bioRxiv.

The Network Framework of Molecular Evolution

Jaume Bertranpetit, Ludovica Montanucci, Hafi Laayouni, 2014 .

Signatures of selection in the human olfactory receptor OR5I1 gene.

Anna Ramírez-Soriano, Francesc Calafell, Jaume Bertranpetit, 2007, Molecular biology and evolution.

Evolutionary Trajectories of Complex Traits in European Populations of Modern Humans

Manoj Kumar Gupta, L. Joosten, M. Netea, 2022, Frontiers in Genetics.

Y-chromosomal sequences of diverse Indian populations and the ancestry of the Andamanese

C. Tyler-Smith, Yali Xue, P. Majumder, 2017, Human Genetics.

Genomic analysis of Andamanese provides insights 1 into ancient human migration into Asia and 2 adaptation 3 4

Qibin Li, M. Pybus, D. Comas, 2016 .

Genome-wide signatures of male-mediated migration shaping the Indian gene pool

Li Jin, Laxmi Parida, Tatiana V Tatarinova, 2015, Journal of Human Genetics.

The dawn of human matrilineal diversity.

Jaume Bertranpetit, Saharon Rosset, David Comas, 2008, American journal of human genetics.

A genomic analysis identifies a novel component in the genetic structure of sub-Saharan African populations

D. Comas, J. Bertranpetit, M. Sikora, 2011, European Journal of Human Genetics.

Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean

D. Comas, J. Bertranpetit, G. Lefranc, 2003, Annals of human genetics.

Worldwide genetic analysis of the CFTR region.

K. Kidd, J. Kidd, A. Pakstis, 2001, American journal of human genetics.

Trading genes along the silk road: mtDNA sequences and the origin of central Asian populations.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, American journal of human genetics.

mtDNA analysis of the Galician population: a genetic edge of European variation

D. Comas, J. Bertranpetit, Á. Carracedo, 1998, European Journal of Human Genetics.

Genetic diversity in the Iberian Peninsula determined from mitochondrial sequence analysis

A. Cambon-Thomsen, J. Bertranpetit, B. Sykes, 1996, Annals of human genetics.

Human mitochondrial DNA variation and the origin of Basques

P. Underhill, D. Comas, J. Bertranpetit, 1995, Annals of human genetics.

Molecular dating of caprines using ancient DNA sequences of Myotragus balearicus, an extinct endemic Balearic mammal

C. Lalueza-Fox, T. Marquès-Bonet, J. Bertranpetit, 2005, BMC Evolutionary Biology.

Heterogeneous rate of protein evolution in serotonin genes.

A. Andrés, C. de Hemptinne, J. Bertranpetit, 2007, Molecular biology and evolution.

Dynamic sensitivity and nonlinear interactions influence the system-level evolutionary patterns of phototransduction proteins

J. Bertranpetit, L. Montanucci, B. Invergo, 2015, Proceedings of the Royal Society B: Biological Sciences.

METABOLIC FLUX IS A DETERMINANT OF THE EVOLUTIONARY RATES OF ENZYME‐ENCODING GENES

J. Bertranpetit, H. Laayouni, L. Montanucci, 2014, Evolution; international journal of organic evolution.

Profiles of accepted mutation: from neutrality in a pseudogene to disease-causing mutation on its homologous gene

J. Bertranpetit, R. Martínez-Arias, F. Calafell, 2001, Human Genetics.

Network-level and population genetics analysis of the insulin/TOR signal transduction pathway across human populations.

P. Luisi, J. Bertranpetit, M. Sikora, 2012, Molecular biology and evolution.

Microsatellites provide evidence for Y chromosome diversity among the founders of the New World.

D. Goldstein, G. Bedoya, A. Ruiz-Linares, 1999, Proceedings of the National Academy of Sciences of the United States of America.

The Mediterranean Paradox for Susceptibility Factors in Coronary Heart Disease Extends to Genetics

I. Dupanloup, J. Bertranpetit, O. Lao, 2007, Annals of human genetics.

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.

Enhancers with tissue-specific activity are enriched in intronic regions

R. Guigó, J. Bertranpetit, Sílvia Pérez-Lluch, 2021, Genome research.

Intronic enhancers regulate the expression of genes involved in tissue-specific functions and homeostasis

R. Guigó, J. Bertranpetit, H. Laayouni, 2020, bioRxiv.

Ethiopia: between Sub-Saharan Africa and western Eurasia.

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

Serotonin Transporter Gene and Risk for Bipolar Affective Disorder: An Association Study in a Spanish Population

R. Murray, D. Collier, B. Gutiérrez, 1998, Biological Psychiatry.

Genetic variation of the 5-HT2A receptor gene and bipolar affective disorder

D. Collier, B. Gutiérrez, V. Vallès, 1997, Human Genetics.

Evolutionary analysis of genes of two pathways involved in placental malaria infection

J. Bertranpetit, M. Sikora, F. Casals, 2008, Human Genetics.

A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300

Jaume Bertranpetit, Fernando Muñoz, Maria Esteve, 2012, Gut.

Population structure in copy number variation and SNPs in the CCL4L chemokine gene

D. Comas, M. Juan, J. Bertranpetit, 2008, Genes and Immunity.

Human Genome Variation and the Concept of Genotype Networks

Giovanni Marco Dall'Olio, Jaume Bertranpetit, Hafid Laayouni, 2013, PloS one.

Variation in short tandem repeats is deeply structured by genetic background on the human Y chromosome.

C. Tyler-Smith, A. Pérez-Lezaun, D. Comas, 1999, American journal of human genetics.

Molecular evolution and network-level analysis of the N-glycosylation metabolic pathway across primates.

Giovanni Marco Dall'Olio, Jaume Bertranpetit, Hafid Laayouni, 2011, Molecular biology and evolution.

Prion susceptibility and protective alleles exhibit marked geographic differences

K. Stefánsson, A. Andrés, J. Yagüe, 2003, Human mutation.

Extreme population differences across Neuregulin 1 gene, with implications for association studies

D. Comas, A. González-Neira, J. Bertranpetit, 2006, Molecular Psychiatry.

An assessment of a massively parallel sequencing approach for the identification of individuals from mass graves of the Spanish Civil War (1936–1939)

Francesc Calafell, Jaume Bertranpetit, Roger Anglada, 2016, Electrophoresis.

VCF2Networks: applying genotype networks to single-nucleotide variants data

Giovanni Marco Dall'Olio, Jaume Bertranpetit, Hafid Laayouni, 2014, Bioinform..

Correction: Human Genome Variation and the Concept of Genotype Networks

A. Wagner, J. Bertranpetit, H. Laayouni, 2014, PLoS ONE.

Comparative Genetics of Functional Trinucleotide Tandem Repeats in Humans and Apes

A. Andrés, N. Saitou, H. Jacobs, 2004, Journal of Molecular Evolution.

Pseudogenes: Patterns of Mutation

J. Bertranpetit, R. Martínez-Arias, F. Calafell, 2006 .

Cosmic phylogeny: reconstructing the chemical history of the solar neighbourhood with an evolutionary tree

J. Bertranpetit, R. Foley, P. Das, 2016, 1611.02575.

A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis.

D. Absher, R. Myers, J. Gisbert, 2014, Human molecular genetics.

A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes

J. Bertranpetit, Y. Parman, L. Kalaydjieva, 2005, Journal of Medical Genetics.

Distribution of events of positive selection and population differentiation in a metabolic pathway: the case of asparagine N-glycosylation

P. Luisi, J. Bertranpetit, M. Sikora, 2012, BMC Evolutionary Biology.

Allele frequencies of 13 short tandem repeats in population samples from the Iberian Peninsula and Northern Africa

A. Pérez-Lezaun, J. Bertranpetit, J. Clarimón, 2000, International Journal of Legal Medicine.

A genome-wide survey does not show the genetic distinctiveness of Basques

J. Bertranpetit, F. Calafell, H. Laayouni, 2010, Human Genetics.

Balancing Selection Is the Main Force Shaping the Evolution of Innate Immunity Genes1

T. Marquès-Bonet, J. Bertranpetit, A. Navarro, 2008, The Journal of Immunology.

HLA evidence for the lack of genetic heterogeneity in Basques

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, Annals of human genetics.

HLA class I and class II DNA typing and the origin of Basques.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1998, Tissue antigens.

Nucleotide substitution rates for the full set of mitochondrial protein-coding genes in Coleoptera.

J. Bertranpetit, J. Pons, I. Ribera, 2010, Molecular phylogenetics and evolution.

The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild

Arcadi Navarro, Jaume Bertranpetit, Can Alkan, 2013, BMC Genomics.

Positive Selection in Human Populations: Practical Aspects and Current Knowledge

P. Luisi, M. Pybus, J. Bertranpetit, 2021 .

Recombination networks as genetic markers in a human variation study of the Old World

M. Netea, Asif Javed, M. Pybus, 2012, Human Genetics.

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.

X. Estivill, J. Bertranpetit, T. Casals, 1993, Human molecular genetics.

Can a place of origin of the main cystic fibrosis mutations be identified?

J. Bertranpetit, T. Casals, F. Calafell, 2002, American journal of human genetics.

Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene

K. Kidd, J. Kidd, J. Bertranpetit, 1999, Human Heredity.

Sex-specific migration patterns in Central Asian populations, revealed by analysis of Y-chromosome short tandem repeats and mtDNA.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1999, American journal of human genetics.

This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon.

Jaume Bertranpetit, Hafid Laayouni, Ludovica Montanucci, 2011 .

HLA-G genetic diversity and evolutive aspects in worldwide populations

J. Bertranpetit, M. Passos-Bueno, M. Zatz, 2021, Scientific Reports.

A Natural History of FUT 2 Polymorphism in Humans

J. Bertranpetit, M. Sikora, F. Casals, 2009 .

The genetics of East African populations: a Nilo-Saharan component in the African genetic landscape

A. Zhernakova, C. Wijmenga, M. Netea, 2015, Scientific Reports.

Chromosome X-wide Analysis of Positive Selection in Human Populations: Common and Private Signals of Selection and its Impact on Inactivated Genes and Enhancers

J. Bertranpetit, Jessica Nye, H. Laayouni, 2021, Frontiers in Genetics.

Positive selection in admixed populations from Ethiopia

C. Tyler-Smith, L. Pagani, Yali Xue, 2020, BMC Genetics.

Hierarchical boosting: a machine-learning framework to detect and classify hard selective sweeps in human populations

Giovanni Marco Dall'Olio, Jaume Bertranpetit, Hafid Laayouni, 2015, Bioinform..

Origins, admixture and founder lineages in European Roma

M. Netea, D. Comas, J. Bertranpetit, 2015, European Journal of Human Genetics.

Georgian and kurd mtDNA sequence analysis shows a lack of correlation between languages and female genetic lineages.

L. Fañanás, D. Comas, J. Bertranpetit, 2000, American journal of physical anthropology.

Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages

D. Comas, J. Bertranpetit, O. Lao, 2004, European Journal of Human Genetics.

Gene connectivity and enzyme evolution in the human metabolic network

J. Bertranpetit, J. Peretó, H. Laayouni, 2019, Biology Direct.

Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits

M. Stoneking, M. Batzer, A. Sajantila, 2000, Human Genetics.

Principal component analysis of gene frequencies and the origin of Basques.

J. Bertranpetit, F. Calafell, 1994, American journal of physical anthropology.

SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data

Francesc Calafell, Arcadi Navarro, Jaume Bertranpetit, 2008, Bioinform..

From the detection of population structure to the reconstruction of population history: the historical reading of the human genome

J. Bertranpetit, H. Laayouni, 2009, Heredity.

Structure of linkage disequilibrium in humans: genome factors and population stratification.

D. Comas, A. González-Neira, J. Bertranpetit, 2003, Cold Spring Harbor symposia on quantitative biology.

Seasonality of birth in schizophrenia. An insufficient stratification of control population?

L. Fañanás, J. Bertranpetit, J. L. Martí-Tusquets, 1989, Social psychiatry and psychiatric epidemiology.

Palmar flexion creases in schizophrenia

L. Fañanás, J. Bertranpetit, P. Moral, 1991 .

Evidence for a Common Origin of Most Friedreich Ataxia Chromosomes in the Spanish Population

M. Koenig, J. Bertranpetit, R. Frutos, 1996, European journal of human genetics : EJHG.

Molecular phylogeny and evolution of the extinct bovid Myotragus balearicus.

C. Lalueza-Fox, J. Bertranpetit, B. Shapiro, 2002, Molecular phylogenetics and evolution.

1000 Genomes Selection Browser 1.0: a genome browser dedicated to signatures of natural selection in modern humans

Pavlos Pavlidis, Giovanni Marco Dall'Olio, Jaume Bertranpetit, 2013, Nucleic Acids Res..

Estimating the Ancestral Recombinations Graph (ARG) as Compatible Networks of SNP Patterns

Francesc Calafell, Laxmi Parida, Jaume Bertranpetit, 2008, J. Comput. Biol..

Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study.

Jaume Bertranpetit, Richard M Myers, Fernando Muñoz, 2015, Gastroenterology.

Aboriginal Australian mitochondrial genome variation – an increased understanding of population antiquity and diversity

Nirav C. Merchant, R. J. Mitchell, C. Tyler-Smith, 2017, Scientific Reports.

Functional role of positively selected amino acid substitutions in mammalian rhodopsin evolution

P. Garriga, J. Bertranpetit, B. Invergo, 2016, Scientific Reports.

Variability in the serotonin transporter gene and increased risk for major depression with melancholia

B. Gutiérrez, L. Fañanás, J. Bertranpetit, 1998, Human Genetics.

Radiation and phylogeography in the Japanese macaque, Macaca fuscata.

J. Bertranpetit, J. Terradas, O. Takenaka, 2004, Molecular phylogenetics and evolution.

Reply to ‘No evidence for unknown archaic ancestry in South Asia’

J. Bertranpetit, F. Casals, M. Mondal, 2018, Nature Genetics.

Further confirmation for unknown archaic ancestry in Andaman and South Asia

P. Majumder, J. Bertranpetit, F. Casals, 2016, bioRxiv.

Authors' reply: How is causal interference practised in the biological sciences?

X. Estivill, F. Real, J. Bertranpetit, 2000 .

The origin of the major cystic fibrosis mutation (delta F508) in European populations.

X. Estivill, J. Bertranpetit, L. Kalaydjieva, 1994, Nature genetics.

Genetic structure of north-west Africa revealed by STR analysis

A. Pérez-Lezaun, D. Comas, A. Cambon-Thomsen, 2000, European Journal of Human Genetics.

Evolution of cytokine production capacity in ancient and modern European populations

M. Jaeger, L. Joosten, M. Netea, 2021, bioRxiv.

Spatial patterns of cystic fibrosis mutation spectra in European populations

A. Andrés, J. Bertranpetit, O. Lao, 2003, European Journal of Human Genetics.

Population history of north Africa: evidence from classical genetic markers.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human biology.

Human mitochondrial DNA sequence variation in the Moroccan population of the Souss area

D. Comas, J. Bertranpetit, F. Calafell, 2001, Annals of human biology.

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population

C. Gieger, A. Hofman, A. Uitterlinden, 2009, European Journal of Human Genetics.

Insights into the western Bantu dispersal: mtDNA lineage analysis in Angola

D. Comas, J. Bertranpetit, Á. Carracedo, 2004, Human Genetics.

Minimizing recombinations in consensus networks for phylogeographic studies

Francesc Calafell, Laxmi Parida, Jaume Bertranpetit, 2009, BMC Bioinformatics.

Genetic origins, singularity, and heterogeneity of Basques

D. Comas, J. Bertranpetit, B. Oyharçabal, 2021, Current Biology.

Variation in estimated recombination rates across human populations

D. Balding, A. González-Neira, J. Bertranpetit, 2007, Human Genetics.

Microsatellite variation and the differentiation of modern humans

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1996, Human Genetics.

Approximate Bayesian computation with deep learning supports a third archaic introgression in Asia and Oceania

J. Bertranpetit, O. Lao, M. Mondal, 2019, Nature Communications.

Reply to ‘No evidence for unknown archaic ancestry in South Asia’

P. Majumder, J. Bertranpetit, F. Casals, 2018, Nature Genetics.

Glucocerebrosidase pseudogene variation and Gaucher disease: Recognizing pseudogene tracts in GBA alleles

D. Comas, J. Bertranpetit, R. Martínez-Arias, 2001, Human mutation.

Population and genomic lessons from genetic analysis of two Indian populations

P. Luisi, J. Bertranpetit, P. Heutink, 2014, Human Genetics.

Human F7 sequence is split into three deep clades that are related to FVII plasma levels

L. Almasy, J. Blangero, J. Bertranpetit, 2006, Human Genetics.

Recent Radiation of R‐M269 and High Y‐STR Haplotype Resemblance Confirmed

D. Comas, J. Bertranpetit, F. Calafell, 2014, Annals of human genetics.

Genetic and geographical variability in cystic fibrosis: evolutionary considerations.

J. Bertranpetit, F. Calafell, Jaume Bertranpetit, 1996, Ciba Foundation symposium.

Geographic variation in human mitochondrial DNA control region sequence: the population history of Turkey and its relationship to the European populations.

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1996, Molecular biology and evolution.

The annotation of the asparagine N-linked glycosylation pathway in the Reactome database.

Giovanni Marco Dall'Olio, Jaume Bertranpetit, Hafid Laayouni, 2011, Glycobiology.

Incipient GAA repeats in the primate Friedreich ataxia homologous genes.

J. Bertranpetit, M. Moltó, J. Cañizares, 1999, Molecular biology and evolution.

Exploring the rate-limiting steps in visual phototransduction recovery by bottom-up kinetic modeling

J. Bertranpetit, K. Koch, D. Dell’Orco, 2013, Cell Communication and Signaling.

Isolated populations as treasure troves in genetic epidemiology: the case of the Basques

A. González-Neira, J. Bertranpetit, M. Sikora, 2009, European Journal of Human Genetics.

The genetics of pre-Roman Iberian Peninsula: A mtDNA study of ancient Iberians

C. Lalueza-Fox, D. Comas, J. Bertranpetit, 2006 .

Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.

J. Bertranpetit, E. Coto, L. Kalaydjieva, 2008, Molecular immunology.

The shaping of immunological responses through natural selection after the Roma Diaspora

M. Netea, D. Comas, R. ter Horst, 2020, Scientific Reports.

Haplotype tagging efficiency in worldwide populations in CTLA4 gene

D. Comas, J. Bertranpetit, O. Lao, 2005, Genes and Immunity.

Convergent evolution in European and Rroma populations reveals pressure exerted by plague on Toll-like receptors

M. Oosting, L. Joosten, A. Zhernakova, 2014, Proceedings of the National Academy of Sciences.

A genome-wide association study identifies SLC8A3 as a susceptibility locus for ACPA-positive rheumatoid arthritis.

D. Absher, R. Myers, J. Gelpí, 2016, Rheumatology.

SEASONALITY OF MARRIAGES IN SPANISH AND FRENCH PARISHES IN THE CERDANYA VALLEY, EASTERN PYRENEES

J. Bertranpetit, H. Macbeth, M. Salvat, 1997, Journal of Biosocial Science.

PKLR-GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations

A. Andrés, A. Pérez-Lezaun, J. Bertranpetit, 2002, Human Genetics.

Quantitative dermatoglyphics in schizophrenia: study of family history subgroups.

L. Fañanás, J. Bertranpetit, P. Moral, 1990, Human biology.

Chromosome X-wide analysis of positive selection in human populations: from common and private signals to selection impact on inactivated genes and enhancers-like signatures

J. Bertranpetit, Jessica Nye, H. Laayouni, 2021, bioRxiv.

Y-chromosomal Diversity in Europe Is Clinal and Influenced Primarily by Geography, Rather than by Language

R. J. Mitchell, C. Tyler-Smith, M. Hurles, 2022 .

mtDNA hypervariable region II (HVII) sequences in human evolution studies

J. Bertranpetit, Á. Carracedo, A. Salas, 2000, European Journal of Human Genetics.

Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania

Nirav C. Merchant, R. J. Mitchell, C. Tyler-Smith, 2016, Journal of Human Genetics.

Assessing the signatures of selection in PRNP from polymorphism data: results support Kreitman and Di Rienzo's opinion.

K. Stefánsson, Agnar Helgason, J. Bertranpetit, 2005, Trends in genetics : TIG.

Determination of Haploid DNA Sequences in Humans: Application to the Glucocerebrosidase Pseudogene

D. Comas, J. Bertranpetit, R. Martínez-Arias, 2002, DNA sequence : the journal of DNA sequencing and mapping.

Geographic homogeneity and non-equilibrium patterns of mtDNA sequences in Tuscany, Italy.

J. Bertranpetit, G. Bertorelle, G. Barbujani, 1996 .

Geographic homogeneity and non-equilibrium patterns of mtDNA sequences in Tuscany, Italy

J. Bertranpetit, G. Bertorelle, G. Barbujani, 1996, Human Genetics.

Ethiopia: between Sub‐Saharan Africa and Western Eurasia

D. Labuda, J. Bertranpetit, C. Moreau, 2005 .

Recent insertion of an Alu element within a polymorphic human-specific Alu insertion.

A Sajantila, A. Sajantila, D. Comas, 2001, Molecular biology and evolution.

Extreme individual marker FST values do not imply population-specific selection in humans: the NRG1 example

Francesc Calafell, Arcadi Navarro, Jaume Bertranpetit, 2007, Human Genetics.

Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations.

M. Stoneking, J. Bertranpetit, A. Navarro, 2009, Molecular biology and evolution.

Report and Geographic Structure in Europe

C. Gieger, T. Werge, M. Nelson, 2022 .

A comprehensive model of the phototransduction cascade in mouse rod cells.

J. Bertranpetit, K. Koch, D. Dell’Orco, 2014, Molecular bioSystems.

Network-level and population genetics analysis of the insulin/TOR signal transduction pathway across human populations.

P. Luisi, J. Bertranpetit, M. Sikora, 2012, Molecular biology and evolution.

A Targeted Association Study of Immunity Genes and Networks Suggests Novel Associations with Placental Malaria Infection

M. Netea, C. Menéndez, J. Bertranpetit, 2011, PloS one.

A New Method to Reconstruct Recombination Events at a Genomic Scale

Francesc Calafell, Laxmi Parida, Jaume Bertranpetit, 2010, PLoS Comput. Biol..

A natural history of FUT2 polymorphism in humans.

J. Bertranpetit, M. Sikora, F. Casals, 2009, Molecular biology and evolution.

Morphometric, Behavioral, and Genomic Evidence for a New Orangutan Species

B. Goossens, A. Scally, C. Groves, 2017, Current Biology.

Morphometric, Behavioral, and Genomic Evidence for a New Orangutan Species

B. Goossens, A. Scally, C. Groves, 2017, Current Biology.

Mitochondrial DNA variation and the origin of the Europeans

A. Pérez-Lezaun, D. Comas, J. Bertranpetit, 1997, Human Genetics.

Genetics and population history. The case of the Iberian Peninsula and the “origin” of Basques

J. Bertranpetit, 2022, Human Population Genetics and Genomics.

Agta hunter–gatherer oral microbiomes are shaped by contact network structure

J. Gómez-Gardeñes, V. Latora, M. Greenacre, 2023, Evolutionary Human Sciences.

Signatures of genetic variation in human microRNAs point to processes of positive selection and population-specific disease risks

J. Bertranpetit, H. Laayouni, Y. Espinosa-Parrilla, 2021, Human Genetics.

Is There Selection for the Pace of Successive Inactivation of the arpAT Gene in Primates?

D. Torrents, J. Bertranpetit, F. Casals, 2008, Journal of Molecular Evolution.

Population structure in copy number variation and SNPs in the CCL4L chemokine gene

D. Comas, M. Juan, J. Bertranpetit, 2008, Genes and Immunity.

The prion protein gene in humans revisited: lessons from a worldwide resequencing study.

A. Andrés, J. Bertranpetit, A. Navarro, 2005, Genome research.

This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. Genetic characterization of the ABO blood group in Neandertals

A. Rosas, J. Fortea, J. Bertranpetit, 2008 .

Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22

H. Cann, D. Comas, A. González-Neira, 2004, Human Genomics.