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Human Molecular Genetics|April 2, 2003
How a Hedgehog might see holoprosencephalyErich Roessler, Maximilian MuenkeAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Abnormal sterol metabolism in holoprosencephalyDorothea Haas, Maximilian MuenkeAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 18, 2018
Syndromes associated with holoprosencephalyPaul Kruszka, Maximilian MuenkeAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
The molecular genetics of holoprosencephalyErich Roessler, Maximilian MuenkeHuman Genetics|August 16, 2011
Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHHDaniel E Pineda-Alvarez, Erich Roessler, Ping Hu, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literatureAmelia A Keaton, Benjamin D Solomon, Anthonie J van Essen, et al.American Journal of Medical Genetics. Part A|May 27, 2010
Deletion of 8q24 in an adult with mild dysmorphic features, developmental delay, and ketotic hypoglycemiaBenjamin D Solomon, Eileen Lange, Jay Shubrook, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literatureEmily F Kauvar, Benjamin D Solomon, Cynthia J R Curry, et al.Molecular Genetics & Genomic Medicine|January 8, 2016
Foreword to volume 3, issue 6P Suzanne Hart, Maximilian MuenkeAttention Deficit and Hyperactivity Disorders|March 25, 2011
Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHDMauricio Arcos-Burgos, Maximilian MuenkePageof 29