List of works - Danuta Z Loesch

A new anthropometric scale for discrimination between sexes

scientific article published on 01 March 1992

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

scientific article published in November 2005

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

scientific article published in April 2006

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

scientific article published in April 2007

Behavioural and cognitive phenotypes in idiopathic autism versus autism associated with fragile X syndrome

scientific article published in November 2008

Clinical features and reproductive patterns in fragile X female heterozygotes ⬇️

scientific article published on June 1, 1988

Common Genetic Variants Influence Whorls in Fingerprint Patterns

scientific article

Comparative study of sole patterns in chromosomal abnormalities ⬇️

scientific article published on 01 June 1970

Dermatoglyphic distances and position of 21 trisomy mosaics ⬇️

scientific article published on December 1, 1979

Dermatoglyphic patterns in 9p trisomy syndrome

scientific article published on 01 March 1978

Dermatoglyphic sole patterns in 21 trisomics ⬇️

scientific article published on 01 March 1983

Dermatoglyphic total patterns on palms, finger-tips and soles in twins

scientific article published on September 1, 1978

Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: a case-control study

scientific article

Discriminant analysis of dermatoglyphic measurements in fragile X males and females ⬇️

scientific article published on 01 March 1988

Discriminant diagnosis of 21-trisomy mosaicism ⬇️

scientific article published on September 1, 1976

Discriminant functions and 21-trisomy mosaicism ⬇️

scientific article published on October 1, 1975

Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots

scientific article published on 28 April 2014

Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.

scientific article

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

scientific article published in December 2002

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

scientific article published in October 2003

Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females

scientific article published on 01 July 2018

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

scientific article

Experience with direct molecular diagnosis of fragile X ⬇️

scientific article published on June 1, 1992

FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles

scientific article

Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy

scientific article published on November 15, 1992

Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.

scientific article published on 10 January 2012

Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

scientific article

Genetical distance and dermatoglyphic characters. II. Intrapopulation distance coefficients

scientific article published on 01 January 1978

Genetical studies of the palmar and sole patterns and some derrnatoǵlyphic measurements in twins ⬇️

scientific article published on July 1, 1979

Growth in stature and head circumference in high-functioning autism and Asperger disorder during the first 3 years of life

scientific article published in January 2006

Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS).

scientific article published on 23 April 2012

Immortalized Parkinson's disease lymphocytes have enhanced mitochondrial respiratory activity

scientific article published on 16 September 2016

Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS).

scientific article published on 15 June 2006

Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome

scientific article published in April 2007

Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disorders

scientific article

Limb development genes underlie variation in human fingerprint patterns

scientific article published on 01 January 2022

Linkage analysis of a model quantitative trait in humans: finger ridge count shows significant multivariate linkage to 5q14.1.

scientific article

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

scientific article published in October 2009

Magnetic resonance imaging study in older fragile X premutation male carriers

scientific article published in August 2005

Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome.

scientific article published on September 2010

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

scientific article

Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia Syndrome.

scientific article

Phenotypic variation and FMRP levels in fragile X.

scientific article published on January 2004

Problems in ascertainment of transmitting males in Martin-Bell syndrome ⬇️

scientific article published on December 15, 1991

Relationship of birth weight and length with growth in height and body diameters from 5 years of age to maturity

scientific article published in November 1999

Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert

scientific article

Ridgecounter: a program for obtaining semi-automated finger ridge counts

scientific article

Search for heterozygosis in quantitative characters

scientific article published on July 1, 1978

Skeletal Growth Dysregulation in Australian Male Infants and Toddlers With Autism Spectrum Disorder.

scientific article published on 6 April 2018

The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) Markers

scholarly article by Danuta Z Loesch et al published 2018 in Frontiers in Genetics

Topological formulation of finger-tip patterns: comparison of complete and incomplete 21 trisomics with normal subjects ⬇️

scientific article published on 01 June 1975

Topologically significant dermatoglyphic patterns in twins

scientific article published on January 1, 1977

Total and Regional White Matter Lesions Are Correlated With Motor and Cognitive Impairments in Carriers of the FMR1 Premutation

scientific article published on 13 August 2019

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

scientific article published on 11 August 2006

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study

scientific article published on 24 December 2013

List of works by Danuta Z Loesch

A new anthropometric scale for discrimination between sexes

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

Behavioural and cognitive phenotypes in idiopathic autism versus autism associated with fragile X syndrome

Clinical features and reproductive patterns in fragile X female heterozygotes ⬇️

Common Genetic Variants Influence Whorls in Fingerprint Patterns

Comparative study of sole patterns in chromosomal abnormalities ⬇️

Dermatoglyphic distances and position of 21 trisomy mosaics ⬇️

Dermatoglyphic patterns in 9p trisomy syndrome

Dermatoglyphic sole patterns in 21 trisomics ⬇️

Dermatoglyphic total patterns on palms, finger-tips and soles in twins

Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: a case-control study

Discriminant analysis of dermatoglyphic measurements in fragile X males and females ⬇️

Discriminant diagnosis of 21-trisomy mosaicism ⬇️

Discriminant functions and 21-trisomy mosaicism ⬇️

Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots

Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis.

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

Experience with direct molecular diagnosis of fragile X ⬇️

FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles

Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy

Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.

Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

Genetical distance and dermatoglyphic characters. II. Intrapopulation distance coefficients

Genetical studies of the palmar and sole patterns and some derrnatoǵlyphic measurements in twins ⬇️

Growth in stature and head circumference in high-functioning autism and Asperger disorder during the first 3 years of life

Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS).

Immortalized Parkinson's disease lymphocytes have enhanced mitochondrial respiratory activity

Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS).

Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome

Improved methodology for assessment of mRNA levels in blood of patients with FMR1 related disorders

Limb development genes underlie variation in human fingerprint patterns

Linkage analysis of a model quantitative trait in humans: finger ridge count shows significant multivariate linkage to 5q14.1.

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

Magnetic resonance imaging study in older fragile X premutation male carriers

Methylation analysis of fragile X-related epigenetic elements may provide a suitable newborn screening test for fragile X syndrome.

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia Syndrome.

Phenotypic variation and FMRP levels in fragile X.

Problems in ascertainment of transmitting males in Martin-Bell syndrome ⬇️

Relationship of birth weight and length with growth in height and body diameters from 5 years of age to maturity

Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert

Ridgecounter: a program for obtaining semi-automated finger ridge counts

Search for heterozygosis in quantitative characters

Skeletal Growth Dysregulation in Australian Male Infants and Toddlers With Autism Spectrum Disorder.

The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) Markers

Topological formulation of finger-tip patterns: comparison of complete and incomplete 21 trisomics with normal subjects ⬇️

Topologically significant dermatoglyphic patterns in twins

Total and Regional White Matter Lesions Are Correlated With Motor and Cognitive Impairments in Carriers of the FMR1 Premutation

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study