Erica E Davis

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 22

Top Venues

Nature communications

American journal of medical genetics. Part A

Science advances

medRxiv : the preprint server for health sciences

Ann & Robert H. Lurie Children's Hospital of Chicago

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

Affiliation History

Ann & Robert H. Lurie Children's Hospital of Chicago Sep 01 2019

United States

Associate Professor :: Advanced Center for Translational Genomic Medicine (ACT-GeM)

Duke University Jul 01 2016 - Aug 31 2019

United States

Associate Professor :: Center for Human Disease Modeling

Duke University Nov 01 2009 - Jun 30 2016

United States

Assistant Professor :: Center for Human Disease Modeling

Publications

Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti, Zaineb Akram, Imran Khan Yousafzai, Wajahat Bin Naeem, Nasreen Fatima, Asmat Ali, Zafar Iqbal, Ayaz Khan, Muhammad Shahzad, Chunyu Liu, Mathias Toft, Feng Zhang, Muhammad Tariq, Erica E Davis, Tahir N Khan
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN. Molecular genetics and genomics : MGG 299 (1) (2024)
Jana Willim, Daniel Woike, Daniel Greene, Sarada Das, Kevin Pfeifer, Weimin Yuan, Anika G Lindsey, Omar Itani, Amber L Böhme, Debora Tibbe, Hans-Hinrich Hönck, Fatemeh Hassani Nia, null null, Michael Zech, Theresa Brunet, Laurence Faivre, Arthur Sorlin, Antonio Vitobello, Thomas Smol, Cindy Colson, Kristin Baranano, Krista Schatz, Carolina Alvarez, Kelly Schoch, Rebecca Spillmann, Erica E Davis, Erin Conboy, Francesco Vetrini, Konrad Platzer, Sonja Neuser, Janina Gburek-Augustat, Alexandra Noel Grace, Bailey Mitchell, Alexander P A Stegmann, Margje Sinnema, Naomi Meeks, Carol J Saunders, Maxime Cadieux-Dion, Juliane Hoyer, Julien Van Gils, Jean-Madeleine de Sainte-Agathe, Michelle L Thompson, E Martina Bebin, Monika Weisz-Hubshman, Anne-Claude Tabet, Alain Verloes, Jonathan Lévy, Xenia Latypova, Sönke Harder, Gary A Silverman, Stephen C Pak, Tim Schedl, Kathleen Freson, Andrew Mumford, Ernest Turro, Christian Schlein, Vandana Shashi, Hans-Jürgen Kreienkamp
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors. Nature communications 15 (1) (2024)
Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti, Zaineb Akram, Imran Khan Yousafzai, Wajahat Bin Naeem, Nasreen Fatima, Asmat Ali, Zafar Iqbal, Ayaz Khan, Muhammad Shahzad, Chunyu Liu, Mathias Toft, Feng Zhang, Muhammad Tariq, Erica E Davis, Tahir N Khan
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN. Molecular genetics and genomics : MGG 299 (1) (2024)
Kimberly A Chapman, Farid Ullah, Zachary A Yahiku, Sri Varsha Kodiparthi, Georgios Kellaris, Sandrina P Correia, Tommy Stödberg, Christalena Sofokleous, Nikolaos M Marinakis, Helena Fryssira, Eirini Tsoutsou, Jan Traeger-Synodinos, Andrea Accogli, Vincenzo Salpietro, Pasquale Striano, Seth I Berger, Kelvin W Pond, Suman Sirimulla, Erica E Davis, Martha R C Bhattacharya
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome via alteration of metabolic signaling. medRxiv : the preprint server for health sciences (2024)
Kimberly A Chapman, Farid Ullah, Zachary A Yahiku, Sri Varsha Kodiparthi, Georgios Kellaris, Sandrina P Correia, Tommy Stödberg, Christalena Sofokleous, Nikolaos M Marinakis, Helena Fryssira, Eirini Tsoutsou, Jan Traeger-Synodinos, Andrea Accogli, Vincenzo Salpietro, Pasquale Striano, Seth I Berger, Kelvin W Pond, Suman Sirimulla, Erica E Davis, Martha R C Bhattacharya
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome via alteration of metabolic signaling. medRxiv : the preprint server for health sciences (2024)
Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Sheraz Khan, Ina Ofelia Focșa, Magdalena Budișteanu, Cristina Stoica, Florina Nedelea, Laurențiu Bohîlțea, Lavinia Caba, Lăcrămioara Butnariu, Monica Pânzaru, Cristina Rusu, Claudia Jurcă, Adela Chiriță-Emandi, Claudia Bănescu, Wasim Abbas, Azita Sadeghpour, Shahid Mahmood Baig, Mihaela Bălgrădean, Erica E Davis
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants. American journal of medical genetics. Part A (2023)
Sarah C Harris, Karen Chong, David Chitayat, Kelly L Gilmore, Alexander Augusto de Lima Jorge, Bruna L Freire, Antonio Marcondes Lerario, Patrick Shannon, Heidi Cope, William B Gallentine, Gwenal Le Guyader, Frederic Bilan, Pascaline Létard, Erica E Davis, Neeta L Vora
Diagnosis of TBC1D32-associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy. American journal of medical genetics. Part A (2023)
Laura J Grange, John J Reynolds, Farid Ullah, Bertrand Isidor, Robert F Shearer, Xenia Latypova, Ryan M Baxley, Antony W Oliver, Anil Ganesh, Sophie L Cooke, Satpal S Jhujh, Gavin S McNee, Robert Hollingworth, Martin R Higgs, Toyoaki Natsume, Tahir N Khan, Gabriel Á Martos-Moreno, Sharon Chupp, Christopher G Mathew, David A Parry, Michael A Simpson, Nahid Nahavandi, Zafer Yüksel, Mojgan Drasdo, Anja Kron, Petra Vogt, Annemarie Jonasson, Saad Ahmed Seth, Claudia Gonzaga-Jauregui, Karlla W Brigatti, Alexander P A Stegmann, Masato T Kanemaki, Dragana Josifova, Yuri Uchiyama, Yukiko Oh, Akira Morimoto, Hitoshi Osaka, Zineb Ammous, Jesús Argente, Naomichi Matsumoto, Constance T R M Stumpel, Alexander Malcolm Taylor, Andrew P Jackson, Anja-Katrin Bielinsky, Niels Mailand, Cedric Le Caignec, Erica E Davis, Grant S Stewart
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy. Nature communications 13 (1) (2022)
Chuyi Chen, Yuyang Gu, Julien Philippe, Peiran Zhang, Hunter Bachman, Jinxin Zhang, John Mai, Joseph Rufo, John F Rawls, Erica E Davis, Nicholas Katsanis, Tony Jun Huang
Acoustofluidic rotational tweezing enables high-speed contactless morphological phenotyping of zebrafish larvae. Nature communications 12 (1) (2021)
Farid Ullah, Waqar Rauf, Kamal Khan, Sheraz Khan, Katrina M Bell, Vanessa Cristina de Oliveira, Muhammad Tariq, Shabnam Bakhshalizadeh, Philippe Touraine, Nicholas Katsanis, Andrew Sinclair, Sijie He, Elena J Tucker, Shahid M Baig, Erica E Davis
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss. Human genetics 140 (12) (2021)
Kamal Khan, Sarmad Mehmood, Chunyu Liu, Maimoona Siddiqui, Arsalan Ahmad, Belqees Yawar Faiz, Barry A Chioza, Emma A Baple, Muhammad I Ullah, Zaineb Akram, Humayoon S Satti, Raees Khan, Gaurav V Harlalka, Muhammad Jameel, Talia Akram, Shahid M Baig, Andrew H Crosby, Muhammad J Hassan, Feng Zhang, Erica E Davis, Tahir N Khan
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees. American journal of medical genetics. Part A (2021)
Maria Kousi, Onuralp Söylemez, Aysegül Ozanturk, Niki Mourtzi, Sebastian Akle, Irwin Jungreis, Jean Muller, Christopher A Cassa, Harrison Brand, Jill Anne Rosenfeld, Maxim Y Wolf, Azita Sadeghpour, Kelsey McFadden, Richard A Lewis, Michael E Talkowski, Hélène Dollfus, Manolis Kellis, Erica E Davis, Shamil R Sunyaev, Nicholas Katsanis
Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy. Nature genetics 52 (11) (2020)
Gerard W Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen, Yayoi Ikawa, Karsten Boldt, Asaf Ta-Shma, Isabella Aprea, Katsura Minegishi, Yuan-Ping Pang, Petra Pennekamp, Niki T Loges, Johanna Raidt, Rim Hjeij, Julia Wallmeier, Huda Mussaffi, Zeev Perles, Orly Elpeleg, Franziska Rabert, Hidetaka Shiratori, Stef J Letteboer, Nicola Horn, Samuel Young, Timo Strünker, Friederike Stumme, Claudius Werner, Heike Olbrich, Katsuyoshi Takaoka, Takahiro Ide, Wang Kyaw Twan, Luisa Biebach, Jörg Große-Onnebrink, Judith A Klinkenbusch, Kavita Praveen, Diana C Bracht, Inga M Höben, Katrin Junger, Jana Gützlaff, Sandra Cindrić, Micha Aviram, Thomas Kaiser, Yasin Memari, Petras P Dzeja, Bernd Dworniczak, Marius Ueffing, Ronald Roepman, Kerstin Bartscherer, Nicholas Katsanis, Erica E Davis, Israel Amirav, Hiroshi Hamada, Heymut Omran
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module. Nature communications 11 (1) (2020)
Yu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, Sujata Srikanth, Nicola A Thompson, Mercedes Calvo Pardo, Lu Yu, Joy W Norris, Yunhui Peng, Karen W Gripp, Kirk A Aleck, Chumei Li, Ed Spence, Tae-Ik Choi, Soo Jeong Kwon, Hee-Moon Park, Daseuli Yu, Seokhwi Kim, Marie R Mooney, Shahid M Baig, Ingrid M Wentzensen, Aida Telegrafi, Kirsty McWalter, Trevor A Moreland, Chelsea Roadhouse, Keri Ramsey, Michael J Lyons, Cindy Skinner, Emil Alexov, Nicholas Katsanis, Roger E Stevenson, Jyoti Sharma Choudhary, David J Adams, Cheol-Hee Kim, Erica E Davis, Charles E Schwartz
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nature communications 11 (1) (2020)
Kamal Khan, Michael Zech, Angela T Morgan, David J Amor, Matej Skorvanek, Tahir N Khan, Michael S Hildebrand, Victoria E Jackson, Thomas S Scerri, Matthew Coleman, Kristin A Rigbye, Ingrid Eileen Scheffer, Melanie Bahlo, Matias Wagner, Daniel D Lam, Riccardo Berutti, Petra Havránková, Anna Fečíková, Tim M Strom, Vladimir Han, Petra Dosekova, Zuzana Gdovinova, Franco Laccone, Muhammad Jameel, Marie R Mooney, Shahid Mahmood Baig, Robert Jech, Erica E Davis, Nicholas Katsanis, Juliane Winkelmann
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Shuji Mizumoto, Andreas R Janecke, Azita Sadeghpour, Gundula Povysil, Marie T McDonald, Sheila Unger, Susanne Greber-Platzer, Kristen L Deak, Nicholas Katsanis, Andrea Superti-Furga, Kazuyuki Sugahara, Erica E Davis, Shuhei Yamada, Julia Vodopiutz
CSGALNACT1-congenital disorder of glycosylation: A mild skeletal dysplasia with advanced bone age. Human mutation 41 (3) (2019)
I-Chun Tsai, Kelly McKnight, Spencer U McKinstry, Andrew T Maynard, Perciliz L Tan, Christelle Golzio, C Thomas White, Daniel J Price, Erica E Davis, Heather Amrine-Madsen, Nicholas Katsanis
Small molecule inhibition of RAS/MAPK signaling ameliorates developmental pathologies of Kabuki Syndrome. Scientific reports 8 (1) (2018)
Sara Huston Katsanis, Mollie A Minear, Azita Sadeghpour, Heidi Cope, Yezmin Perilla, Robert M Cook-Deegan, null null, Nicholas Katsanis, Erica E Davis, Misha Angrist
Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions. Journal of participatory medicine 10 (1) (2018)
Benjamin M Helm, Jason R Willer, Azita Sadeghpour, Christelle Golzio, Eric Crouch, Samantha Schrier Vergano, Nicholas Katsanis, Erica E Davis
Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome. Human genomics 11 (1) (2017)
Mary R Hutson, Anna L Keyte, Miriam Hernández-Morales, Eric Gibbs, Zachary A Kupchinsky, Ioannis Argyridis, Kyle N Erwin, Kelly Pegram, Margaret Kneifel, Paul B Rosenberg, Pavle Matak, Luke Xie, Jörg Grandl, Erica E Davis, Nicholas Katsanis, Chunlei Liu, Eric J Benner
Temperature-activated ion channels in neural crest cells confer maternal fever-associated birth defects. Science signaling 10 (500) (2017)
Susan S Brooks, Alissa L Wall, Christelle Golzio, David W Reid, Amalia Kondyles, Jason R Willer, Christina Botti, Christopher V Nicchitta, Nicholas Katsanis, Erica E Davis
A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans. Genetics 198 (2) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Erica E Davis