Christian Patrick Schaaf (Christian P Schaaf, C P Schaaf, Chun-An Chen)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 51

Top Venues

American journal of medical genetics. Part A

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

Disease models & mechanisms

AJNR. American journal of neuroradiology

UniversitätsKlinikum Heidelberg

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

Affiliation History

UniversitätsKlinikum Heidelberg Apr 01 2019

Germany

Professor and Chairman :: Institute of Human Genetics

Publications

Tim Schubert, Christian Patrick Schaaf
MAGEL2 (patho-)physiology and Schaaf-Yang syndrome. Developmental medicine and child neurology (2024)
Elena Schnabel-Besson, Ulrike Mütze, Nicola Dikow, Friederike Hörster, Marina A Morath, Karla Alex, Heiko Brennenstuhl, Sascha Settegast, Jürgen G Okun, Christian Patrick Schaaf, Eva C Winkler, Stefan Kölker
Wilson and Jungner Revisited: Are Screening Criteria Fit for the 21st Century? International journal of neonatal screening 10 (3) (2024)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome. Disease models & mechanisms 16 (2) (2023)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome. Disease models & mechanisms 16 (2) (2023)
Nilesh K Desai, Stephen F Kralik, J C Edmond, V Shah, Thierry A G M Huisman, M Rech, Christian Patrick Schaaf
Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR. American journal of neuroradiology 44 (2) (2023)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome. Disease models & mechanisms 16 (2) (2023)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome. Disease models & mechanisms 16 (2) (2023)
Nilesh K Desai, Stephen F Kralik, J C Edmond, V Shah, Thierry A G M Huisman, M Rech, Christian Patrick Schaaf
Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR. American journal of neuroradiology (2023)
Nilesh K Desai, Stephen F Kralik, J C Edmond, V Shah, Thierry A G M Huisman, M Rech, Christian Patrick Schaaf
Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR. American journal of neuroradiology 44 (2) (2023)
Laura Dötsch, Lisa Matesevac, Theresa V Strong, Christian Patrick Schaaf
Caregiver-based perception of disease burden in Schaaf-Yang syndrome. Molecular genetics & genomic medicine (2023)
Nilesh K Desai, Stephen F Kralik, J C Edmond, V Shah, Thierry A G M Huisman, M Rech, Christian Patrick Schaaf
Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR. American journal of neuroradiology 44 (2) (2023)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome. Disease models & mechanisms 16 (2) (2023)
Derek L Reznik, Mingxiao V Yang, Pedro Albelda de la Haza, Antrix Jain, Melanie Spanjaard, Susanne Theiss, Christian Patrick Schaaf, Anna Malovannaya, Theresa V Strong, Surabi Veeraragavan, Rodney C Samaco
Truncated rat Magel2 modelled for the study of Schaaf-Yang syndrome alters select behavioral and physiological outcomes. Disease models & mechanisms (2023)
Michele Bertacchi, Chiara Tocco, Christian Patrick Schaaf, Michèle Studer
Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome. Cells 11 (8) (2022)
Ferdinand Althammer, Françoise Muscatelli, Valery Grinevich, Christian Patrick Schaaf
Oxytocin-based therapies for treatment of Prader-Willi and Schaaf-Yang syndromes: evidence, disappointments, and future research strategies. Translational psychiatry 12 (1) (2022)
Sarah Catrin Titgemeyer, Christian Patrick Schaaf
Facebook Support Groups for Pediatric Rare Diseases: Cross-Sectional Study to Investigate Opportunities, Limitations, and Privacy Concerns. JMIR pediatrics and parenting 5 (1) (2022)
Jeremy M Schraw, Renata H Benjamin, Charles J Shumate, Mark A Canfield, Daryl A Scott, Scott D McLean, Hope Northrup, Angela E Scheuerle, Christian Patrick Schaaf, Joseph W Ray, Han Chen, A J Agopian, Philip J Lupo
Patterns of co-occurring birth defects in children with anotia and microtia. American journal of medical genetics. Part A 191 (3) (2022)
Ferdinand Althammer, Moritz Claudius Wimmer, Quirin Krabichler, Stephanie Küppers, Jonas Schimmer, Henning Fröhlich, Laura Dötsch, Tim Gruber, Selina Wunsch, Tim Schubert, Matthew K Kirchner, Javier E Stern, Alexandre Charlet, Valery Grinevich, Christian Patrick Schaaf
Analysis of the hypothalamic oxytocin system and oxytocin receptor-expressing astrocytes in a mouse model of Prader-Willi syndrome. Journal of neuroendocrinology (2022)
Jeremy M Schraw, Renata H Benjamin, Charles J Shumate, Mark A Canfield, Daryl A Scott, Scott D McLean, Hope Northrup, Angela E Scheuerle, Christian Patrick Schaaf, Joseph W Ray, Han Chen, A J Agopian, Philip J Lupo
Patterns of co-occurring birth defects in children with anotia and microtia. American journal of medical genetics. Part A (2022)
Jeremy M Schraw, Renata H Benjamin, Charles J Shumate, Mark A Canfield, Daryl A Scott, Scott D McLean, Hope Northrup, Angela E Scheuerle, Christian Patrick Schaaf, Joseph W Ray, Han Chen, A J Agopian, Philip J Lupo
Patterns of co-occurring birth defects in children with anotia and microtia. American journal of medical genetics. Part A 191 (3) (2022)
Felix Marbach, Beata S Lipska-Ziętkiewicz, Agata Knurowska, Vincent Michaud, Henri Margot, James Lespinasse, Frédéric Tran Mau Them, Christine Coubes, Joohyun Park, Sarah Grosch, Cristiana Roggia, Ute Grasshoff, Louisa Kalsner, Anne Sophie Denommé-Pichon, Alexandra Afenjar, Bénédicte Héron, Boris Keren, Pilar Caro, Christian Patrick Schaaf
Phenotypic characterization of seven individuals with Marbach-Schaaf neurodevelopmental syndrome. American journal of medical genetics. Part A 188 (9) (2022)
Jeremy M Schraw, Renata H Benjamin, Charles J Shumate, Mark A Canfield, Daryl A Scott, Scott D McLean, Hope Northrup, Angela E Scheuerle, Christian Patrick Schaaf, Joseph W Ray, Han Chen, A J Agopian, Philip J Lupo
Patterns of co-occurring birth defects in children with anotia and microtia. American journal of medical genetics. Part A 191 (3) (2022)
Jeremy M Schraw, Renata H Benjamin, Charles J Shumate, Mark A Canfield, Daryl A Scott, Scott D McLean, Hope Northrup, Angela E Scheuerle, Christian Patrick Schaaf, Joseph W Ray, Han Chen, A J Agopian, Philip J Lupo
Patterns of co-occurring birth defects in children with anotia and microtia. American journal of medical genetics. Part A 191 (3) (2022)
Felix Marbach, Georgi Stoyanov, Florian Erger, Constantine A Stratakis, Nikolaos Settas, Edra London, Jill A Rosenfeld, Erin Torti, Chad Haldeman-Englert, Evgenia Sklirou, Elena Kessler, Sophia Ceulemans, Stanley F Nelson, Julian A Martinez-Agosto, Christina G S Palmer, Rebecca H Signer, null null, Marisa V Andrews, Dorothy K Grange, Rebecca Willaert, Richard Person, Aida Telegrafi, Aaron Sievers, Magdalena Laugsch, Susanne Theiß, YuZhu Cheng, Olivier Lichtarge, Panagiotis Katsonis, Amber Stocco, Christian Patrick Schaaf
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain. Genetics in medicine : official journal of the American College of Medical Genetics 23 (8) (2021)
Peter Horak, Jonas Leichsenring, Hannah Goldschmid, Simon Kreutzfeldt, Daniel Kazdal, Veronica Teleanu, Volker Endris, Laura Gieldon, Michael Allgäuer, Anna-Lena Volckmar, Nicola Dikow, Marcus Renner, Martina Kirchner, Roland Penzel, Carolin Ploeger, Regine Brandt, Huriye Seker-Cin, Jan Budczies, Christoph E Heilig, Olaf Neumann, Christian Patrick Schaaf, Peter Schirmacher, Stefan Fröhling, Albrecht Stenzinger
Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine. Genes, chromosomes & cancer (2021)
Christian Patrick Schaaf, Stefan Kölker, Georg F Hoffmann
Genomic newborn screening: Proposal of a two-stage approach. Journal of inherited metabolic disease 44 (3) (2021)
Nils R Hebach, Pilar Caro, Bailey A Martin-Giacalone, Philip J Lupo, Felix Marbach, Daniela Choukair, Christian Patrick Schaaf
A retrospective analysis of growth hormone therapy in children with Schaaf-Yang syndrome. Clinical genetics 100 (3) (2021)
Clara Velmans, Anne H O'Donnell-Luria, Emanuela Argilli, Frédéric Tran Mau Them, Antonio Vitobello, Marcus Cy Chan, Jasmine Lee-Fong Fung, Megan Rech, Angela Abicht, Marion Aubert-Mucca, Jason Carmichael, Nicolas Chassaing, Robin Clark, Christine Coubes, Anne Sophie Denommé-Pichon, John Karl de Dios, Eleina England, Benoit Funalot, Marion Gerard, Maries Joseph, Colleen Kennedy, Camille Kumps, Marjolaine Willems, Ingrid M B H van de Laar, Coranne Aarts-Tesselaar, Marjon van Slegtenhorst, Daphne Lehalle, Kathleen Leppig, Lennart Lessmeier, Lynn S Pais, Heather Paterson, Subhadra Ramanathan, Lance H Rodan, Andrea Superti-Furga, Brian Hon-Yin Chung, Elliott Sherr, Christian Netzer, Christian Patrick Schaaf, Florian Erger
O'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum. Journal of medical genetics (2021)
Steffen Hirsch, Laura Gieldon, Christian Sutter, Nicola Dikow, Christian Patrick Schaaf
Germline testing for homologous recombination repair genes-opportunities and challenges. Genes, chromosomes & cancer 60 (5) (2020)
Megan E Rech, John M McCarthy, Chun-An Chen, Jane C Edmond, Veeral S Shah, Daniëlle G M Bosch, Gerard T Berry, Linford Williams, Suneeta Madan-Khetarpal, Dmitriy Niyazov, Charles Shaw-Smith, Erin M Kovar, Philip J Lupo, Christian Patrick Schaaf
Phenotypic expansion of Bosch-Boonstra-Schaaf optic atrophy syndrome and further evidence for genotype-phenotype correlations. American journal of medical genetics. Part A 182 (6) (2020)
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, Cristina Martínez, Ralph Röth, Thomas Thumberger, Volker Eckstein, Jutta Scheuerer, Cornelia Thöni, Felix Lasitschka, Leonie Carstensen, Patrick Günther, Stefan G Holland-Cunz, Robert M W Hofstra, Erwin Brosens, Jill Anne Rosenfeld, Christian Patrick Schaaf, Duco Schriemer, Isabella Ceccherini, Marta Rusmini, Joseph Tilghman, Berta Luzón-Toro, Ana Torroglosa, Salud Borrego, Clara Sze Man Tang, Mercè Garcia-Barceló, Paul Tam, Nagarajan Paramasivam, Melanie Bewerunge-Hudler, Carolina de la Torre, Norbert Gretz, Gudrun A Rappold, Philipp Romero, Beate Niesler
A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease. PLoS genetics 16 (11) (2020)
Christian Patrick Schaaf, Catalina Betancur, Ryan K C Yuen, Jeremy R Parr, David H Skuse, Louise Gallagher, Raphael A Bernier, Janet A Buchanan, Joseph D Buxbaum, Chun-An Chen, Kira A Dies, Mayada Elsabbagh, Helen V Firth, Thomas Frazier, Ny Hoang, Jennifer Howe, Christian R Marshall, Jacques L Michaud, Olivia Rennie, Peter Szatmari, Wendy K Chung, Patrick F Bolton, Edwin H Cook, Stephen W Scherer, Jacob A S Vorstman
A framework for an evidence-based gene list relevant to autism spectrum disorder. Nature reviews. Genetics 21 (6) (2020)
Sarah Catrin Titgemeyer, Christian Patrick Schaaf
Facebook Support Groups for Rare Pediatric Diseases: Quantitative Analysis. JMIR pediatrics and parenting 3 (2) (2020)
Felix Marbach, Christian Patrick Schaaf
Response to Briuglia et al. Genetics in medicine : official journal of the American College of Medical Genetics 23 (2) (2020)
Michael D Fountain, David S Oleson, Megan E Rech, Lara Segebrecht, Jill V Hunter, John M McCarthy, Philip J Lupo, Manuel Holtgrewe, Rocio Moran, Jill A Rosenfeld, Bertrand Isidor, Cédric Le Caignec, Margarita S Saenz, Robert C Pedersen, Thomas M Morgan, Jean P Pfotenhauer, Fan Xia, Weimin Bi, Sung-Hae L Kang, Ankita Patel, Ian D Krantz, Sarah E Raible, Wendy Smith, Ingrid Cristian, Erin Torti, Jane Juusola, Francisca Millan, Ingrid M Wentzensen, Richard E Person, Sébastien Küry, Stéphane Bézieau, Kévin Uguen, Claude Férec, Arnold Munnich, Mieke van Haelst, Klaske D Lichtenbelt, Koen van Gassen, Tanner Hagelstrom, Aditi Chawla, Denise L Perry, Ryan J Taft, Marilyn Jones, Diane Masser-Frye, David Dyment, Sunita Venkateswaran, Chumei Li, Luis F Escobar, Denise Horn, Rebecca C Spillmann, Loren Peña, Jolanta Wierzba, Tim M Strom, Ilaria Parenti, Frank J Kaiser, Nadja Ehmke, Christian Patrick Schaaf
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. Genetics in medicine : official journal of the American College of Medical Genetics 21 (8) (2019)
Shiguo Liu, Miaomiao Tian, Fan He, Jiani Li, Hong Xie, Wenmiao Liu, Yeting Zhang, Ru Zhang, Mingji Yi, Fengyuan Che, Xu Ma, Yi Zheng, Hao Deng, Guiju Wang, Lang Chen, Xue Sun, Yinglei Xu, Jingli Wang, Yucui Zang, Mengmeng Han, Xiuhai Wang, Hongzai Guan, Yinlin Ge, Chunmei Wu, Haiyan Wang, Hui Liang, Hui Li, Ni Ran, Zhaochuan Yang, Huanhuan Huang, Yanzhao Wei, Xueping Zheng, Xiangrong Sun, Xueying Feng, Lanlan Zheng, Tao Zhu, Wenhan Luo, Qinan Chen, Yuze Yan, Zuzhou Huang, Zhongcui Jing, Yixia Guo, Xuzhan Zhang, Christian Patrick Schaaf, Jinchuan Xing, Chuanyue Wang, Fuli Yu, Ji-Song Guan
Mutations in ASH1L confer susceptibility to Tourette syndrome. Molecular psychiatry 25 (2) (2019)
Emeline Crutcher, Rituraj Pal, Fatemeh Naini, Ping Zhang, Magdalena Laugsch, Jean J Kim, Aleksandar Bajic, Christian Patrick Schaaf
mTOR and autophagy pathways are dysregulated in murine and human models of Schaaf-Yang syndrome. Scientific reports 9 (1) (2019)
Shen Gu, Chun-An Chen, Jill A Rosenfeld, Heidi Cope, Nathalie Launay, Kevin M Flanigan, Megan A Waldrop, Rachel Schrader, Jane Juusola, Ozlem Goker-Alpan, Aubrey Milunsky, Agatha Schlüter, Mónica Troncoso, Aurora Pujol, Queenie K-G Tan, Christian Patrick Schaaf, Linyan Meng
Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia. Human mutation 41 (3) (2019)
Elena Martín-Hernández, María Elena Rodríguez-García, Chun-An Chen, Francisco Javier Cotrina-Vinagre, Patricia Carnicero-Rodríguez, Marcello Bellusci, Christian Patrick Schaaf, Francisco Martínez-Azorín
Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation. Journal of human genetics 63 (4) (2018)
John McCarthy, Philip J Lupo, Erin Kovar, Megan Rech, Bret Bostwick, Daryl Scott, Katerina Kraft, Tony Roscioli, Joel Charrow, Samantha A Schrier Vergano, Edward Lose, Robert Smiegel, Yves Lacassie, Christian Patrick Schaaf
Schaaf-Yang syndrome overview: Report of 78 individuals. American journal of medical genetics. Part A 176 (12) (2018)
Madelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, Christian Patrick Schaaf
An estimation of the prevalence of genomic disorders using chromosomal microarray data. Journal of human genetics 63 (7) (2018)
M D Fountain, H Tao, C-A Chen, J Yin, Christian Patrick Schaaf
Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty. Genes, brain, and behavior 16 (6) (2017)
M A Gillentine, L N Berry, R P Goin-Kochel, M A Ali, J Ge, D Guffey, J A Rosenfeld, V Hannig, P Bader, M Proud, M Shinawi, B H Graham, A Lin, S R Lalani, J Reynolds, M Chen, T Grebe, C G Minard, P Stankiewicz, A L Beaudet, Christian Patrick Schaaf
The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. Journal of autism and developmental disorders 47 (3) (2017)
Xia Wang, Wu-Lin Charng, Chun-An Chen, Jill A Rosenfeld, Aisha Al Shamsi, Lihadh Al-Gazali, Marianne McGuire, Nicholas Ah Mew, Georgianne L Arnold, Chunjing Qu, Yan Ding, Donna M Muzny, Richard A Gibbs, Christine M Eng, Magdalena Walkiewicz, Fan Xia, Sharon E Plon, James R Lupski, Christian Patrick Schaaf, Yaping Yang
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations. Nature genetics 49 (4) (2017)
Xiqian Jiang, Jianwei Chen, Aleksandar Bajić, Chengwei Zhang, Xianzhou Song, Shaina L Carroll, Zhao-Lin Cai, Meiling Tang, Mingshan Xue, Ninghui Cheng, Christian Patrick Schaaf, Feng Li, Kevin R MacKenzie, Allan Chris M Ferreon, Fan Xia, Meng C Wang, Mirjana Maletić-Savatić, Jin Wang
Quantitative real-time imaging of glutathione. Nature communications 8 (2017)
Maria Helgeson, Jennifer Keller-Ramey, Amy Knight Johnson, Jennifer A Lee, Daniel B Magner, Brett Deml, Jacea Deml, Ying-Ying Hu, Zejuan Li, Kirsten Donato, Soma Das, Rachel Laframboise, Sandra Tremblay, Ian Krantz, Sarah Noon, George Hoganson, Jennifer Burton, Christian Patrick Schaaf, Daniela Del Gaudio
Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome. Journal of human genetics 63 (3) (2017)
Hsiang-Chih Lu, Qiumin Tan, Maxime W C Rousseaux, Wei Wang, Ji-Yoen Kim, Ronald Richman, Ying-Wooi Wan, Szu-Ying Yeh, Jay M Patel, Xiuyun Liu, Tao Lin, Yoontae Lee, John D Fryer, Jing Han, Maria H Chahrour, Richard H Finnell, Yunping Lei, Maria E Zurita-Jimenez, Priyanka Ahimaz, Kwame Anyane-Yeboa, Lionel Van Maldergem, Daphne Lehalle, Nolwenn Jean-Marcais, Anne-Laure Mosca-Boidron, Julien Thevenon, Margot A Cousin, Della E Bro, Brendan C Lanpher, Eric W Klee, Nora Alexander, Matthew N Bainbridge, Harry T Orr, Roy V Sillitoe, M Cecilia Ljungberg, Zhandong Liu, Christian Patrick Schaaf, Huda Y Zoghbi
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nature genetics 49 (4) (2017)
Christian Patrick Schaaf, Daniëlle G M Bosch, Megan T Cho, Jill A Rosenfeld, Jill Anne Rosenfeld, Richard Alan Lewis, Richard Alan Lewis, Parul Jayakar, Katelyn Payne, Laurence Walsh, Timothy Moss, Allison Schreiber, Cheri Schoonveld, Kristin G Monaghan, Frances Elmslie, Ganka Douglas, F Nienke Boonstra, Francisca Millan, Frans P M Cremers, Dianalee McKnight, Gabriele Richard, Jane Juusola, Fran Kendall, Keri Ramsey, Kwame Anyane-Yeboa, Elfrida Malkin, Wendy K Chung, Wendy K Chung, Dmitriy M Niyazov, Magdalena Walkiewicz, Vivekanand Veluchamy, Chumei Li, Fuki M Hisama, Bert B A de Vries, Christian Schaaf
The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations. Genetics in medicine : official journal of the American College of Medical Genetics 18 (11) (2016)
Mark N Ziats, Robin P Goin-Kochel, Leandra N Berry, May Ali, Jun Ge, Danielle Guffey, Jill Anne Rosenfeld, Patricia Bader, Michael J Gambello, Varina Wolf, Lynette S Penney, Ryan Miller, Robert Roger Lebel, Jeffrey Kane, Kristine Bachman, Robin Troxell, Gary Clark, Charles G Minard, Pawel Stankiewicz, Arthur Beaudet, Christian Patrick Schaaf
The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 18 (11) (2016)
Michael D Fountain, Emmelien Aten, Megan T Cho, Jane Juusola, Magdalena A Walkiewicz, Joseph W Ray, Fan Xia, Yaping Yang, Brett H Graham, Carlos A Bacino, Lorraine Potocki, Arie van Haeringen, Claudia A L Ruivenkamp, Pedro Mancias, Hope Northrup, Mary K Kukolich, Marjan M Weiss, Conny M A van Ravenswaaij-Arts, Inge B Mathijssen, Sebastien Levesque, Naomi Meeks, Jill Anne Rosenfeld, Danielle Lemke, Ada Hamosh, M E Suzanne Lewis, Simone Race, Laura L Stewart, Beverly Hay, Andrea M Lewis, Rita L Guerreiro, Jose T Bras, Marcia P Martins, Gerarda Derksen-Lubsen, Els Peeters, Connie Stumpel, Sander Stegmann, Levinus A Bok, Gijs W E Santen, Christian Patrick Schaaf
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genetics in medicine : official journal of the American College of Medical Genetics 19 (1) (2016)
Emeline Crutcher, May Ali, John Harrison, Judit Sovago, Baltazar Gomez-Mancilla, Christian Patrick Schaaf
Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome. Journal of autism and developmental disorders 46 (4) (2016)

Christian Patrick Schaaf.css-eqlu8i{font-size:small;padding-left:4px;} (Christian P Schaaf, C P Schaaf, Chun-An Chen)

Publication Activity (10 Years)

Top Topics

Top Venues

Christian Patrick Schaaf (Christian P Schaaf, C P Schaaf, Chun-An Chen)