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Erich Roessler | doi.page

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Erich Roessler

National Institutes of Health(US)National Human Genome Research Institute(US)

Publications by Year

Research Areas

Hedgehog Signaling Pathway Studies, Congenital limb and hand anomalies, Cleft Lip and Palate Research, Ocular Disorders and Treatments, Developmental Biology and Gene Regulation

Most-Cited Works

→ Mutations in the human Sonic Hedgehog gene cause holoprosencephaly(1996)1,155 cited
→ Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly(1996)645 cited
→ Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly(1999)427 cited
→ 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.(1994)412 cited
→ 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.(1994)397 cited
→ Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination(2000)392 cited

→ The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly(1999)

359 cited

→ Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects(2000)351 cited

→ Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features(2003)344 cited

→ A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication(2010)291 cited