Concepedia

Alfons Meindl

AM

Statistics

Publications

4

Citations

211

H-Index

4

Active since

1993

Affiliations

Heidelberg University(Current)

Karolinska Institutet

German Cancer Research Center

Ludwig-Maximilians-Universität München

Alfons Meindl is an author at Heidelberg University specializing in genetics, life sciences, and medical genetics.

Publications per year

1993–2009

4

Publications

4

Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

Roger L. Milne, Javier Benı́tez, Heli Nevanlinna et al. · JNCI Journal of the National Cancer Institute · 2009 · 107 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

Alfons Meindl, D. Hosenfeld, W Bruckl et al. · Journal of Medical Genetics · 1993 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer

Michael Wirtenberger, Joachim Schmutzhard, Kari Hemminki et al. · Carcinogenesis · 2006 · 40 citations · Full text

Medicine, Genetics, Oncology +16

A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval

Albrecht Klink, Alfons Meindl, Heide Hellebrand et al. · Human Genetics · 1994 · 15 citations

Life Sciences, Genetics, Molecular Genetics +8

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