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Erich Roessler | Researchclopedia

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Erich Roessler

National Institutes of Health

112

Works

10,413

Citations

51

h-index

79

i10-index

Research Topics

Hedgehog Signaling Pathway Studies Congenital limb and hand anomalies Cleft Lip and Palate Research

Affiliations

Kennedy Krieger Institute1996–1996

National Institutes of Health1992–2020

Children's Hospital of Philadelphia1996–2000

Baylor College of Medicine1986–1986

Advisory Board Company (United States)2011–2011

Top Works

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

Erich Roessler,Elena Belloni,et al.

19961,155 citations

Ocular Disorders and Treatments

Developmental Biology and Gene Regulation

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

Elena Belloni,Maximilian Muenke,et al.

1996645 citations

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

Deeann Wallis,Erich Roessler,et al.

1999427 citations

The interleukin (IL) 2 receptor beta chain is shared by IL-2 and a cytokine, provisionally designated IL-T, that stimulates T-cell proliferation and the induction of lymphokine-activated killer cells.

Richard N. Bamford,Angus Grant,et al.

1994413 citations

A lymphokine, provisionally designated interleukin T and produced by a human adult T-cell leukemia line, stimulates T-cell proliferation and the induction of lymphokine-activated killer cells.

J. D. Burton,Richard N. Bamford,et al.

1994397 citations

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

Karen W. Gripp,David Wotton,et al.

2000392 citations

The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly

Luisa Nanni,Jeffrey E. Ming,et al.

1999359 citations

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

Richard N. Bamford,Erich Roessler,et al.

2000351 citations

Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features

Erich Roessler,Yangzhu Du,et al.

2003344 citations