D-Index & Metrics Best Publications

Jane Gitschier

University of California, San Francisco
United States

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Genetics D-index 55 Citations 19,587 143 World Ranking 2742 National Ranking 1195

Research.com Recognitions

Awards & Achievements

2006 - Fellow of John Simon Guggenheim Memorial Foundation

Overview

What is she best known for?

The fields of study Jane Gitschier is best known for:

Gene
DNA
Parkinsonism

As part of her studies on Genetics, Jane Gitschier often connects relevant areas like Thalassemia. Her study brings together the fields of Genetics and Thalassemia. In her papers, she integrates diverse fields, such as Gene and Duchenne muscular dystrophy. She performs integrative Duchenne muscular dystrophy and Gene research in her work. Her research is interdisciplinary, bridging the disciplines of Pathology and Neurodegeneration. She combines Pathology and Disease in her studies. Her Disease study frequently involves adjacent topics like Parkinsonism. In her articles, she combines various disciplines, including Parkinsonism and Neurodegeneration. Her research brings together the fields of Radiology and Hyperintensity.

Her most cited work include:

An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences (790 citations)
Genetic, Clinical, and Radiographic Delineation of Hallervorden–Spatz Syndrome (596 citations)
h CTR1 : A human gene for copper uptake identified by complementation in yeast (504 citations)

What are the main themes of her work throughout her whole career to date

Much of her study explores Genetics relationship to Transporter. Jane Gitschier integrates Gene and Polymerase chain reaction in her studies. Jane Gitschier performs integrative Polymerase chain reaction and Molecular biology research in her work. In her study, she carries out multidisciplinary Molecular biology and Gel electrophoresis research. While working in this field, Jane Gitschier studies both Gel electrophoresis and Temperature gradient gel electrophoresis. Mutation and Missense mutation are two areas of study in which Jane Gitschier engages in interdisciplinary work. She combines Factor IX and Haemophilia A in her studies. In her research, Jane Gitschier performs multidisciplinary study on Haemophilia A and Haemophilia. She conducted interdisciplinary study in her works that combined Haemophilia and Haemophilia B.

Jane Gitschier most often published in these fields:

Genetics (87.50%)
Gene (81.25%)
Molecular biology (43.75%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase.

Christopher Vulpe;Barbara Levinson;Barbara Levinson;Susan Whitney;Seymour Packman.
Nature Genetics (1993)

1579 Citations

Characterization of the human factor VIII gene

Jane Gitschier;William I. Wood;Therese M. Goralka;Karen L. Wion.
Nature (1984)

1416 Citations

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse.

Christopher D. Vulpe;Yien-Ming Kuo;Therese L. Murphy;Lex Cowley.
Nature Genetics (1999)

1330 Citations

Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

William I. Wood;Jane Gitschier;Laurence A. Lasky;Richard M. Lawn.
Proceedings of the National Academy of Sciences of the United States of America (1985)

1177 Citations

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

Scott C. Kogan;Marie Doherty;Jane Gitschier.
The New England Journal of Medicine (1987)

1125 Citations

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.

Delia Lakich;Haig H. Kazazian;Stylianos E. Antonarakis;Stylianos E. Antonarakis;Jane Gitschier.
Nature Genetics (1993)

1076 Citations

Expression of active human factor VIII from recombinant DNA clones

William I. Wood;Daniel J. Capon;Christian C. Simonsen;Dan L. Eaton.
Nature (1984)

904 Citations

A novel pantothenate kinase gene ( PANK2 ) is defective in Hallervorden-Spatz syndrome

Bing Zhou;Shawn K. Westaway;Barbara Levinson;Monique A. Johnson.
Nature Genetics (2001)

809 Citations

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.

Susan J. Hayflick;Shawn K. Westaway;Barbara Levinson;Bing Zhou.
The New England Journal of Medicine (2003)

716 Citations

hCTR1: A human gene for copper uptake identified by complementation in yeast

Bing Zhou;Jane Gitschier.
Proceedings of the National Academy of Sciences of the United States of America (1997)

639 Citations

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Frequent Co-Authors

External Links

Personal Website for Jane Gitschier