Literature DB >> 12635648

2002 William Allen Award address. Introductory speech for Albert de la Chapelle.

Janet D Rowley1.   

Abstract

Mesh：

Year:  2003        PMID： 12635648      PMCID： PMC379215          DOI： 10.1086/346214

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  18 in total

1.  XX SEX CHROMOSOMES IN A HUMAN MALE. FIRST CASE.

Authors:  A DELACHAPELLE; H HORTLING; M NIEMI; J WENNSTROEM
Journal:  Acta Med Scand       Date:  1964

2.  Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.

Authors:  A de la Chapelle; F A Wright
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

3.  Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes.

Authors:  M C Simmler; F Rouyer; G Vergnaud; M Nyström-Lahti; K Y Ngo; A de la Chapelle; J Weissenbach
Journal:  Nature       Date:  1985 Oct 24-30       Impact factor: 49.962

4.  The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.

Authors:  S Ranta; Y Zhang; B Ross; L Lonka; E Takkunen; A Messer; J Sharp; R Wheeler; K Kusumi; S Mole; W Liu; M B Soares; M F Bonaldo; A Hirvasniemi; A de la Chapelle; T C Gilliam; A E Lehesjoki
Journal:  Nat Genet       Date:  1999-10       Impact factor: 38.330

5.  Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males.

Authors:  D C Page; L G Brown; A de la Chapelle
Journal:  Nature       Date:  1987 Jul 30-Aug 5       Impact factor: 49.962

6.  Chromosome Y-specific DNA in related human XX males.

Authors:  D C Page; A de la Chapelle; J Weissenbach
Journal:  Nature       Date:  1985 May 16-22       Impact factor: 49.962

7.  Clues to the pathogenesis of familial colorectal cancer.

Authors:  L A Aaltonen; P Peltomäki; F S Leach; P Sistonen; L Pylkkänen; J P Mecklin; H Järvinen; S M Powell; J Jen; S R Hamilton
Journal:  Science       Date:  1993-05-07       Impact factor: 47.728

8.  Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure.

Authors:  K Aittomäki; J L Lucena; P Pakarinen; P Sistonen; J Tapanainen; J Gromoll; R Kaskikari; E M Sankila; H Lehväslaiho; A R Engel; E Nieschlag; I Huhtaniemi; A de la Chapelle
Journal:  Cell       Date:  1995-09-22       Impact factor: 41.582

9.  Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males.

Authors:  M Andersson; D C Page; A de la Chapelle
Journal:  Science       Date:  1986-08-15       Impact factor: 47.728

10.  The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

Authors:  J Hästbacka; A de la Chapelle; M M Mahtani; G Clines; M P Reeve-Daly; M Daly; B A Hamilton; K Kusumi; B Trivedi; A Weaver
Journal:  Cell       Date:  1994-09-23       Impact factor: 41.582
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  2 in total

1.  Albert de la Chapelle (1933-2020).

Authors:  Amanda Ewart Toland; Heather Hampel
Journal:  Am J Hum Genet       Date:  2021-02-04       Impact factor: 11.025

2.  Janet Davison Rowley, M.D. (1925–2013).

Authors:  Susanne M Gollin; Shalini C Reshmi
Journal:  Am J Hum Genet       Date:  2014-06-05       Impact factor: 11.025
  2 in total

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