Maximilian Muenke (Max Muenke)

Scopus Author ID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Topics

Induced Pluripotent Stem Cells

Autism Spectrum Disorder

Top Venues

bioRxiv : the preprint server for biology

American journal of medical genetics. Part A

Science advances

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Clara M Abdelmalek, Shriya Singh, Blain Fasil, Allison R Horvath, Sarah B Mulkey, Carlos Curé, Maribel Campos, Denise P Cavalcanti, Van T Tong, Marcela Mercado, Marcela Daza, Mónica Marcela Benavides, Jacqueline Acosta, Suzanne M Gilboa, Diana Valencia, Christina L Sancken, Suzanne M Newton, Deolinda M F Scalabrin, Marisa Márcia Mussi-Pinhata, Zilton Farias Meira de Vasconcelos, Nahida Chakhtoura, Jack Moye, Elizabeth J Leslie, Dorothy I Bulas, Gilbert Vezina, Fernanda J P Marques, Marcio Leyser, Miguel Del Campo, Eric Vilain, Roberta L DeBiasi, Tongguang Wang, Avindra Nath, Tarik F Haydar, Maximilian Muenke, Tamer A Mansour, Adre J du Plessis, Jeffrey C Murray, José F Cordero, Youssef A Kousa
Building a growing genomic data repository for maternal and fetal health through the PING Consortium. medRxiv : the preprint server for health sciences (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Adrianna K San Roman, Helen Skaletsky, Alexander K Godfrey, Neha V Bokil, Levi Teitz, Isani Singh, Laura V Blanton, Daniel W Bellott, Tatyana Pyntikova, Julian Lange, Natalia Koutseva, Jennifer F Hughes, Laura Brown, Sidaly Phou, Ashley Buscetta, Paul S Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C Lasutschinkow, Colleen Keen, Shanlee M Davis, Angela E Lin, Nicole R Tartaglia, Carole A Samango-Sprouse, Maximilian Muenke, David C Page
The human Y and inactive X chromosomes similarly modulate autosomal gene expression. bioRxiv : the preprint server for biology (2023)
Slim Mzoughi, Federico Di Tullio, Diana H P Low, Corina-Mihaela Motofeanu, Sheena Li Ming Ong, Heike Wollmann, Cheng Mun Wun, Paul Kruszka, Maximilian Muenke, Friedhelm Hildebrandt, Norris R Dunn, Daniel M Messerschmidt, Ernesto Guccione
PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly. Science advances 6 (2) (2020)
Marcela Henriquez-Henriquez, Maria T Acosta, Ariel F Martinez, Jorge Iván Vélez, Francisco Lopera, David A Pineda, Juan D Palacio, Teresa Quiroga, Tilla S Worgall, Richard J Deckelbaum, Claudio Mastronardi, Brooke S G Molina, null null, Mauricio Arcos-Burgos, Maximilian Muenke
Mutations in sphingolipid metabolism genes are associated with ADHD. Translational psychiatry 10 (1) (2020)
Cedrik Tekendo-Ngongang, Paul S Kruszka, Ariel F Martinez, Maximilian Muenke
Novel heterozygous variants in KMT2D associated with holoprosencephaly. Clinical genetics 96 (3) (2019)
Paul S Kruszka, Tommy Hu, Sungkook Hong, Rebecca Signer, Benjamin Cogné, Betrand Isidor, Sarah E Mazzola, Jacques C Giltay, Koen L I van Gassen, Eleina M England, Lynn Pais, Charlotte W Ockeloen, Pedro A Sanchez-Lara, Esther Kinning, Darius J Adams, Kayla Treat, Wilfredo Torres-Martinez, Maria Francesca Bedeschi, Maria Iascone, Stephanie Blaney, Oliver Bell, Tiong Y Tan, Marie-Ange Delrue, Julie Jurgens, Brenda J Barry, Elizabeth C Engle, Sarah K Savage, Nicole Fleischer, Julian A Martinez, Kym M Boycott, Elaine H Zackai, Maximilian Muenke
Phenotype delineation of ZNF462 related syndrome. American journal of medical genetics. Part A 179 (10) (2019)
Anne M Slavotinek, Maximilian Muenke
Introducing in AJMG Part A: Genetic Syndromes in Adults. American journal of medical genetics. Part A 179 (8) (2019)
Karin Weiss, Hayley P Lazar, Alina Kurolap, Ariel F Martinez, Tamar Paperna, Lior Cohen, Marie F Smeland, Sandra Whalen, Solveig Heide, Boris Keren, Pauline Terhal, Melita Irving, Motoki Takaku, John D Roberts, Robert M Petrovich, Samantha A Schrier Vergano, Amy Kenney, Hanne Hove, Elizabeth DeChene, Shane C Quinonez, Estelle Colin, Alban Ziegler, Melissa Rumple, Mahim Jain, Danielle C Monteil, Elizabeth R Roeder, Kimberly Nugent, Arie van Haeringen, Michael Gambello, Avni Santani, Līvija Medne, Bryan Krock, Cara M Skraban, Elaine H Zackai, Holly A Dubbs, Thomas Smol, Jamal Ghoumid, Michael J Parker, Michael Wright, Peter D Turnpenny, Jill Clayton-Smith, Kay Metcalfe, Hitoshi Kurumizaka, Bruce D Gelb, Hagit Baris Feldman, Philippe M Campeau, Maximilian Muenke, Paul A Wade, Katherine Lachlan
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)