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Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe

Human genetics, 2004-10, Vol.115 (5), p.357-371

2004

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Population Structure in the Mediterranean Basin: A Y Chromosome Perspective

Annals of human genetics, 2006-03, Vol.70 (2), p.207-225

2006

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Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects

Molecular phylogenetics and evolution, 2003-09, Vol.28 (3), p.387-395

2003

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AN EXPERIMENT AT TOR VERGATA UNIVERSITY OF ROME (ITALY)

Cultural studies (London, England), 2003-03, Vol.17 (2), p.300-303

Terrenato, L.

2003

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Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I

American journal of human genetics, 1994-06, Vol.54 (6), p.959-965

1994

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A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area

Annals of human genetics, 2001-07, Vol.65 (4), p.339-349

2001

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A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area

Annals of human genetics, 2001-07, Vol.65 (4), p.339-349

2001

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Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Annals of human genetics, 2000-09, Vol.64 (5), p.395-412

2000

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Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations

Journal of molecular evolution, 1995-12, Vol.41 (6), p.966-973

1995

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Population variation analysis at nine loci containing expressed trinucleotide repeats

Annals of human genetics, 1997-09, Vol.61 (5), p.425-438

1997

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The human Y chromosome shows a low level of DNA polymorphism

Annals of human genetics, 1990-10, Vol.54 (4), p.297-305

1990

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Protection against malaria morbidity : near-fixation of the α-thalassemia gene in a nepalese population

American journal of human genetics, 1991-02, Vol.48 (2), p.390-397

1991

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Red Cell Phosphoglucomutase Polymorphism

Human heredity, 2008-08, Vol.20 (1), p.94-103

2008

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Disequilibrium of multiple DNA markers on the human Y chromosome

Annals of human genetics, 1992-10, Vol.56 (4), p.303-310

1992

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The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus

American journal of human genetics, 1993-08, Vol.53 (2), p.391-400

1993

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Natural selection associated with birth weight. IV. U.S.A. data from 1950 to 1976

Annals of human genetics, 1983-01, Vol.47 (1), p.67-71

TERRENATO, L.

1983

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Natural selection associated with birth weight. VI. Towards the end of the stabilizing component

Annals of human genetics, 1992-05, Vol.56 (2), p.113-118

1992

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Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions

Annals of human genetics, 1996-09, Vol.60 (5), p.423-435

1996

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Molecular characterization of β-thalassemia mutations in Egypt

Human genetics, 1990-08, Vol.85 (3), p.272-274

1990

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Autosomal dominant pure cerebellar ataxia. Neurological and genetic study

Brain (London, England : 1878), 1992-12, Vol.115 ( Pt 6) (6), p.1647-1654

1992

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Y chromosome analysis reveals a sharp genetic boundary in the Carpathian region

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.27-33

2001

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Natural selection associated with birth weight V. The secular relaxation of the stabilizing component

Annals of human genetics, 1987-07, Vol.51 (3), p.205-210

1987

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The EUROGEM map of human chromosome 6

European journal of human genetics : EJHG, 1994, Vol.2 (3), p.214-215

1994

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A new β‐thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides

British journal of haematology, 1991-09, Vol.79 (1), p.90-92

1991

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Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sites

Annals of human genetics, 1987-10, Vol.51 (4), p.329-336

1987

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Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe

Population Structure in the Mediterranean Basin: A Y Chromosome Perspective

Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects

AN EXPERIMENT AT TOR VERGATA UNIVERSITY OF ROME (ITALY)

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I

A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area

A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area

Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations

Population variation analysis at nine loci containing expressed trinucleotide repeats

The human Y chromosome shows a low level of DNA polymorphism

Protection against malaria morbidity : near-fixation of the α-thalassemia gene in a nepalese population

Red Cell Phosphoglucomutase Polymorphism

Disequilibrium of multiple DNA markers on the human Y chromosome

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus

Natural selection associated with birth weight. IV. U.S.A. data from 1950 to 1976

Natural selection associated with birth weight. VI. Towards the end of the stabilizing component

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions

Molecular characterization of β-thalassemia mutations in Egypt

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study

Y chromosome analysis reveals a sharp genetic boundary in the Carpathian region

Natural selection associated with birth weight V. The secular relaxation of the stabilizing component

The EUROGEM map of human chromosome 6

A new β‐thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides

Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sites

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