Concepedia

Janine Wagenstaller

JW

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Publications

11

Citations

1.7K

H-Index

11

Active since

2006

Affiliations

Technical University of Munich(Current)

TUM Klinikum

Helmholtz Zentrum München

Institute of Human Genetics

Radboud University Nijmegen

Janine Wagenstaller is an author at Technical University of Munich specializing in genetics, human genetics, and molecular genetics.

Publications per year

2006–2010

11

Publications

11

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis

Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès et al. · Nature Genetics · 2006 · 526 citations · Full text

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Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Gertrud Eckstein et al. · The American Journal of Human Genetics · 2006 · 373 citations · Full text

, , +16

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

David A. Koolen, Andrew J. Sharp, Jane A. Hurst et al. · Journal of Medical Genetics · 2008 · 217 citations

, , +14

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

Denise Horn, Johannes Kapeller, Núria Rivera‐Bruguès et al. · Human Mutation · 2010 · 145 citations · Full text

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Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation

Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz‐Depiereux et al. · The American Journal of Human Genetics · 2007 · 131 citations · Full text

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