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Showing 1–50 of 1757 results

Advanced filters: Author: Martin Genet Clear advanced filters

Naturally occurring cytotoxic anti-tumour antibodies in sera of congenitally athymic (nude) mice

W. JOHN MARTIN
SUE ELLEN MARTIN
Research07 Jun 1974
Nature

Volume: 249, P: 564-565
X–chromosome inactivation during differentiation of female teratocarcinoma stem cells in vitro

Gail R. Martin
Charles J. Epstein
Sara Cohen
Research01 Jan 1978
Nature

Volume: 271, P: 329-333
Evolution of Lorises and Lemurs

PIERRE CHARLES-DOMINIQUE
ROBERT D. MARTIN
Research18 Jul 1970
Nature

Volume: 227, P: 257-260
Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity

Sam Martin
Allan J Richards
Martin P Snead
Research16 Nov 1999
European Journal of Human Genetics

Volume: 7, P: 807-814
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

A. Benomar
L. Krols
A. Brice
Research01 May 1995
Nature Genetics

Volume: 10, P: 84-88
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3

Christine Van Broeckhoven
Hubert Backhovens
Jean-Jacques Martin
Research01 Dec 1992
Nature Genetics

Volume: 2, P: 335-339
A high resolution deletion map of human chromosome Xp22

Laura Schaefer
Giovanni B. Ferrero
Andrea Ballabio
Research01 Jul 1993
Nature Genetics

Volume: 4, P: 272-279
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

Nathaniel H. Robin
George J. Feldman
Maximilian Muenke
Research01 Dec 1995
Nature Genetics

Volume: 11, P: 459-461
Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3

W.R. McCombie
A. Martin-Gallardo
J.C. Venter
Research01 Aug 1992
Nature Genetics

Volume: 1, P: 348-353
The mottled gene is the mouse homologue of the Menkes disease gene

Barbara Levinson
Christopher Vulpe
Jane Gitschier
Research01 Apr 1994
Nature Genetics

Volume: 6, P: 369-373
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH

James R. Burke
Jan J. Enghild
Warren J. Strittmatter
Research01 Mar 1996
Nature Medicine

Volume: 2, P: 347-350
A genome-wide search for human type 1 diabetes susceptibility genes

June L. Davies
Yoshihiko Kawaguchi
John A. Todd
Research08 Sept 1994
Nature

Volume: 371, P: 130-136
Multiple self–healing squamous epitheliomata (ESS1) mapped to chromosome 9q22–q31 in families with common ancestry

David R. Goudie
Martin A.R. Yuille
Malcolm A. Ferguson-Smith
Research01 Feb 1993
Nature Genetics

Volume: 3, P: 165-169
Dependence of position-effect variegation in Drosophila on dose of a gene encoding an unusual zinc-finger protein

Gunter Reuter
Marianna Giarre
Pierre Spierer
Research15 Mar 1990
Nature

Volume: 344, P: 219-223
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction

Multi-trait genome-wide analyses identify variants associated with comorbid lung diseases. Polygenic scores leveraging shared components of heritable risk improve prediction of asthma, chronic obstructive pulmonary disease and lung cancer in a multi-ancestry cohort.

Yixuan He
Wenhan Lu
Alicia R. Martin
Research21 Jan 2026
Nature Genetics

P: 1-10
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

De novo and inherited dominant variants in genes encoding U4 and U6 small nuclear RNAs are identified in individuals with retinitis pigmentosa. The variants cluster at nucleotide positions distinct from those implicated in neurodevelopmental disorders.

Mathieu Quinodoz
Kim Rodenburg
Carlo Rivolta
ResearchOpen Access09 Jan 2026
Nature Genetics

Volume: 58, P: 169-179
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

Ilja Demuth
Marcin Wlodarski
Martin Digweed
Research31 Oct 2000
European Journal of Human Genetics

Volume: 8, P: 861-868
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

Friedhelm Hildebrandt
Edgar Otto
Matthias Brandis
Research01 Oct 1997
Nature Genetics

Volume: 17, P: 149-153
Direct detection of novel expanded trinucleotide repeats in the human genome

Martin Schalling
Thomas J. Hudson
David E. Housman
Research01 Jun 1993
Nature Genetics

Volume: 4, P: 135-139
A tandem duplication in the D–loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

Martin Brockington
Mary G. Sweeney
Anita E. Harding
Research01 May 1993
Nature Genetics

Volume: 4, P: 67-71
Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD).

Petroula Proitsi
Michelle Lupton
John Powell
ResearchOpen Access26 Oct 2009
Nature Precedings

P: 1
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

V. Timmerman
E. Nelis
C. Van Broeckhoven
Research01 Jun 1992
Nature Genetics

Volume: 1, P: 171-175
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

A. Kamb
D. Shattuck-Eidens
L. A. Cannon-Albright
Research01 Sept 1994
Nature Genetics

Volume: 8, P: 22-26
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

Stephen R. Dlouhy
Karen Hsiao
Bernardino Ghetti
Research01 Apr 1992
Nature Genetics

Volume: 1, P: 64-67
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene

Mike Mullan
Henry Houlden
Fiona Crawford
Research01 Dec 1992
Nature Genetics

Volume: 2, P: 340-342
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome

Asli Silahtaroglu
Frans A Hol
Niels Tommerup
Research12 Mar 1999
European Journal of Human Genetics

Volume: 7, P: 68-76
Localization of cystic fibrosis locus to human chromosome 7cen–q22

Brandon J. Wainwright
Peter J. Scambler
Robert Williamson
Research28 Nov 1985
Nature

Volume: 318, P: 384-385
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome

Heather L. Hinds
Claude T. Ashley
Martin Schalling
Research01 Jan 1993
Nature Genetics

Volume: 3, P: 36-43
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

Stefanie Weber
Katrin Hoffmann
Martin Konrad
Research21 Jun 2000
European Journal of Human Genetics

Volume: 8, P: 414-422
Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia

Igor Vořechovský
Liping Luo
Martin A.R. Yuille
Research01 Sept 1997
Nature Genetics

Volume: 17, P: 96-99
HPRT-deficient (Lesch–Nyhan) mouse embryos derived from germline colonization by cultured cells

Martin Hooper
Kate Hardy
Marilyn Monk
Research25 Mar 1987
Nature

Volume: 326, P: 292-295
A twin-pronged attack on complex traits

Nicholas Martin
Dorret Boomsma
Geoffrey Machin
Comments & Opinion01 Dec 1997
Nature Genetics

Volume: 17, P: 387-392
The Intercistronic Divide: Translation of an Intercistronic Region in the Histidine Operon of Salmonella typhimurium

MATTHEW M. RECHLER
ROBERT G. MARTIN
Research06 Jun 1970
Nature

Volume: 226, P: 908-911
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data

MultiSuSiE is an extension of the Sum of Single Effects fine-mapping model that allows causal effect sizes to vary across ancestries. Applying MultiSuSiE to quantitative traits in All of Us identifies fine-mapped variants not implicated by other methods.

Jordan Rossen
Huwenbo Shi
Alkes L. Price
Research05 Jan 2026
Nature Genetics

Volume: 58, P: 67-76
An integrated map of chromosome 18 CAG trinucleotide repeat loci

Andy J Grierson
Marjon van Groenigen
Frank Baas
Research12 Mar 1999
European Journal of Human Genetics

Volume: 7, P: 12-19
Maternal UPD 20 in a hyperactive child with severe growth retardation

I Chudoba
Y Franke
U Claussen
Research22 Jun 1999
European Journal of Human Genetics

Volume: 7, P: 533-540
Drosophila genes Posterior Sex Combs and Suppressor two of zeste encode proteins with homology to the murine bmi-1 oncogene

Brian P. Brunk
Elisabeth C. Martin
Paul N. Adler
Research26 Sept 1991
Nature

Volume: 353, P: 351-353
Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation

EILEEN M. BRYANT
HOLGER HOEHN
GEORGE M. MARTIN
Research28 Jun 1979
Nature

Volume: 279, P: 795-796
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

Xavier Estivill
Martin Farrall
Brandon J. Wainwright
Research01 Apr 1987
Nature

Volume: 326, P: 840-845
Positive control and autogenous regulation of the nifLA promoter in Klebsiella pneumoniae

Martin Drummond
John Clements
Ray Dixon
Research27 Jan 1983
Nature

Volume: 301, P: 302-307
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2

Martin R. Pollak
Yah-Huei Wu Chou
Christine E. Seidman
Research01 Oct 1993
Nature Genetics

Volume: 5, P: 201-204
Counting absolute number of molecules using unique molecular identifiers

Teemu Kivioja
Anna Vähärautio
Jussi Taipale
ResearchOpen Access14 Apr 2011
Nature Precedings

P: 1
Cultivated Cells from Diagnostic Amniocentesis in Second Trimester Pregnancies. I. Clonal Morphology and Growth Potential

Holger Hoehn
Eileen M Bryant
George M Martin
Research01 Aug 1974
Pediatric Research

Volume: 8, P: 746-754
Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour

Seon Park
Amy Bernard
Daniel A. Haber
Research01 Dec 1993
Nature Genetics

Volume: 5, P: 363-367
The Werner syndrome protein is a DNA helicase

Matthew D. Gray
Jiang-Cheng Shen
Lawrence A. Loeb
Research01 Sept 1997
Nature Genetics

Volume: 17, P: 100-103
Model-fitting approaches to the analysis of human behaviour

L J Eaves
Krystyna A Last
N G Martin
Research01 Dec 1978
Heredity

Volume: 41, P: 249-320
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

Jerome R. Lo Ten Foe
Martin A. Rooimans
Hans Joenje
Research01 Nov 1996
Nature Genetics

Volume: 14, P: 320-323
An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

Erik N. Meyers
Mark Lewandoski
Gail R. Martin
Research01 Feb 1998
Nature Genetics

Volume: 18, P: 136-141
Discovery of powerful transient X-ray source A0620—00 with Ariel V Sky Survey Experiment

MARTIN ELVIS
C. G. PAGE
M. J. L. TURNER
Research23 Oct 1975
Nature

Volume: 257, P: 656-657
The relationship between function and DNA sequence in an intercistronic regulatory region in phage λ

Martin Rosenberg
Donald Court
Daniel L. Wulff
Research01 Mar 1978
Nature

Volume: 272, P: 414-423