Muenke, Maximilian

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

Roessler, E., Belloni, E., Gaudenz, K., Jay, P., Berta, P., Scherer, S. W., Tsui, L.-C., & Muenke, M. (1996) · Nature Genetics

Fetal and Pediatric Neurological DisordersHedgehog Signaling Pathway Studies

Cited by 1,152

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

Muenke, M., Schell, U., Hehr, A., Robin, N. H., Losken, H. W., Schinzel, A., Pulleyn, L. J., Rutland, P., Reardon, W., Malcolm, S., et al. (1994) · Nature Genetics

Craniofacial Disorders and TreatmentsConnective tissue disorders research

Cited by 614

Genetics of population isolates

Arcos‐Burgos, M., & Muenke, M. (2002) · Clinical Genetics

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 271

Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis

Kan, S.-H., Elanko, N., Johnson, D., Cornejo-Roldan, L., Cook, J., Reich, E. W., Tomkins, S., Verloes, A., Twigg, S. R. F., Rannan-Eliya, S., et al. (2002) · The American Journal of Human Genetics

Craniofacial Disorders and TreatmentsConnective tissue disorders research

Cited by 265

Mechanistic and epidemiologic considerations in the evaluation of adverse birth outcomes following gestational exposure to statins

Edison, R. J., & Muenke, M. (2004) · American Journal of Medical Genetics Part A

Pregnancy and Medication ImpactPharmacological Effects and Toxicity Studies

Cited by 206

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

Ribasés, M., Ramos-Quiroga, J. A., Sánchez-Mora, C., Bosch, R., Richarte, V., Palomar, G., Gastaminza, X., Bielsa, A., Arcos-Burgos, M., Muenke, M., et al. (2011) · Genes, Brain and Behavior

Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on Behavior

Cited by 119

Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis

Klopocki, E., Lohan, S., Brancati, F., Koll, R., Brehm, A., Seemann, P., Dathe, K., Stricker, S., Hecht, J., Bosse, K., et al. (2011) · The American Journal of Human Genetics

Congenital limb and hand anomaliesCraniofacial Disorders and Treatments

Cited by 104

Review: Genetics of Attention Deficit/Hyperactivity Disorder

Wallis, D., Russell, H. F., & Muenke, M. (2008) · Journal of Pediatric Psychology

Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on Behavior

Cited by 86

Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions

Acosta, M. T., Castellanos, F. X., Bolton, K. L., Balog, J. Z., Eagen, P., Nee, L., Jones, J., Palacio, L., Sarampote, C., Russell, H. F., et al. (2008) · Journal of the American Academy of Child & Adolescent Psychiatry

Attention Deficit Hyperactivity DisorderChild and Adolescent Psychosocial and Emotional Development

Cited by 82

A common genetic network underlies substance use disorders and disruptive or externalizing disorders

Arcos-Burgos, M., Vélez, J. I., Solomon, B. D., & Muenke, M. (2012) · Human Genetics

Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology

Cited by 58

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD

Jain, M., Vélez, J. I., Acosta, M. T., Palacio, L. G., Balog, J., Roessler, E., Pineda, D., Londoño, A. C., Palacio, J. D., Arbelaez, A., et al. (2012) · Molecular Psychiatry

Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology

Cited by 57

Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening

Murdock, D. R., Donovan, F. X., Chandrasekharappa, S. C., Banks, N., Bondy, C., Muenke, M., & Kruszka, P. (2017) · The Journal of Clinical Endocrinology & Metabolism

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenomics and Rare Diseases

Cited by 34

Turner syndrome in diverse populations

Kruszka, P., Addissie, Y. A., Tekendo‐Ngongang, C., Jones, K. L., Savage, S. K., Gupta, N., Sirisena, N. D., Dissanayake, V. H. W., Paththinige, C. S., Aravena, T., et al. (2020) · American Journal of Medical Genetics Part A

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 27

Clinical epidemiology of congenital heart disease in Nigerian children, 2012–2017

Ekure, E. N., Kalu, N., Sokunbi, O. J., Kruszka, P., Olusegun‐Joseph, A. D., Ikebudu, D., Bala, D., Muenke, M., & Adeyemo, A. (2018) · Birth Defects Research

Congenital Heart Disease StudiesCongenital heart defects research

Cited by 26

Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls

Arcos-Burgos, M., Londoño, A. C., Pineda, D. A., Lopera, F., Palacio, J. D., Arbelaez, A., Acosta, M. T., Vélez, J. I., Castellanos, F. X., & Muenke, M. (2012) · ADHD Attention Deficit and Hyperactivity Disorders

Attention Deficit Hyperactivity DisorderAdvanced MRI Techniques and Applications

Cited by 26

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate

Mastronardi, C. A., Pillai, E., Pineda, D. A., Martinez, A. F., Lopera, F., Velez, J. I., Palacio, J. D., Patel, H., Easteal, S., Acosta, M. T., et al. (2016) · Molecular Psychiatry

Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology

Cited by 19