Caleb P Bupp (Caleb Bupp)

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 26

Top Venues

BMC pediatrics

American journal of medical genetics. Part A

Genes

Children (Basel, Switzerland)

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

Publications

Lacey N Lemke, Caleb P Bupp, Karen L Niemchick
Access to clinical genetic services: An evaluation of patient referral characteristics and identifying barriers in Michigan. Journal of genetic counseling (2024)
Caleb P Bupp, Elizabeth G Ames, Madison K Arenchild, Sara Caylor, David P Dimmock, Joseph D Fakhoury, Padmani Karna, April Lehman, Cristian I Meghea, Vinod K Misra, Danielle A Nolan, Jessica O'Shea, Aditi Sharangpani, Linda S Franck, Andrea Scheurer-Monaghan
Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer. Children (Basel, Switzerland) 10 (1) (2023)
Taylor W Cook, Amy M Wilstermann, Jackson T Mitchell, Nicholas E Arnold, Surender Rajasekaran, Caleb P Bupp, Jeremy W Prokop
Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics. Biomolecules 13 (2) (2023)
Taylor W Cook, Amy M Wilstermann, Jackson T Mitchell, Nicholas E Arnold, Surender Rajasekaran, Caleb P Bupp, Jeremy W Prokop
Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics. Biomolecules 13 (2) (2023)
Taylor W Cook, Amy M Wilstermann, Jackson T Mitchell, Nicholas E Arnold, Surender Rajasekaran, Caleb P Bupp, Jeremy W Prokop
Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics. Biomolecules 13 (2) (2023)
Adam Underwood, Daniel T Rasicci, David Hinds, Jackson T Mitchell, Jacob K Zieba, Joshua Mills, Nicholas E Arnold, Taylor W Cook, Mehdi Moustaqil, Yann Gambin, Emma Sierecki, Frank Fontaine, Sophie Vanderweele, Akansha S Das, William Cvammen, Olivia Sirpilla, Xavier Soehnlen, Kristen Bricker, Maram Alokaili, Morgan Green, Sadie Heeringa, Amy M Wilstermann, Thomas M Freeland, Dinah Qutob, Amy Milsted, Ralf Jauch, Timothy J Triche, Connie M Krawczyk, Caleb P Bupp, Surender Rajasekaran, Mathias Francois, Jeremy W Prokop
Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships. Genes 14 (1) (2023)
Taylor W Cook, Amy M Wilstermann, Jackson T Mitchell, Nicholas E Arnold, Surender Rajasekaran, Caleb P Bupp, Jeremy W Prokop
Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics. Biomolecules 13 (2) (2023)
Maria O Levitin, Lettie E Rawlins, Gabriela Sanchez-Andrade, Osama A Arshad, Stephan C Collins, Stephen J Sawiak, Phillip H Iffland, Malin H L Andersson, Caleb P Bupp, Emma L Cambridge, Eve L Coomber, Ian Ellis, Johanna C Herkert, Holly Ironfield, Logan Jory, Perrine F Kretz, Sarina G Kant, Alexandra Neaverson, Esther Nibbeling, Christine Rowley, Emily Relton, Mark Sanderson, Ethan M Scott, Helen Stewart, Andrew Y Shuen, John Schreiber, Liz Tuck, James Tonks, Thorkild Terkelsen, Conny van Ravenswaaij-Arts, Pradeep Vasudevan, Olivia Wenger, Michael Wright, Andrew Day, Adam Hunter, Minal Patel, Christopher J Lelliott, Peter B Crino, Binnaz Yalcin, Andrew H Crosby, Emma L Baple, Darren W Logan, Matthew E Hurles, Sebastian S Gerety
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes. Brain : a journal of neurology (2023)
Claudia V Aniol, Jeremy W Prokop, Surender Rajasekaran, Spencer Pageau, Sydney K Elizer, Elizabeth A VanSickle, Caleb P Bupp
Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report. BMC pediatrics 23 (1) (2023)
André S Bachmann, Elizabeth A VanSickle, Julianne Michael, Marlie Vipond, Caleb P Bupp
Bachmann-Bupp syndrome and treatment. Developmental medicine and child neurology (2023)
Caleb P Bupp, Elizabeth G Ames, Madison K Arenchild, Sara Caylor, David P Dimmock, Joseph D Fakhoury, Padmani Karna, April Lehman, Cristian I Meghea, Vinod K Misra, Danielle A Nolan, Jessica O'Shea, Aditi Sharangpani, Linda S Franck, Andrea Scheurer-Monaghan
Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer. Children (Basel, Switzerland) 10 (1) (2023)
Claudia V Aniol, Jeremy W Prokop, Surender Rajasekaran, Spencer Pageau, Sydney K Elizer, Elizabeth A VanSickle, Caleb P Bupp
Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report. BMC pediatrics 23 (1) (2023)
Adam Underwood, Daniel T Rasicci, David Hinds, Jackson T Mitchell, Jacob K Zieba, Joshua Mills, Nicholas E Arnold, Taylor W Cook, Mehdi Moustaqil, Yann Gambin, Emma Sierecki, Frank Fontaine, Sophie Vanderweele, Akansha S Das, William Cvammen, Olivia Sirpilla, Xavier Soehnlen, Kristen Bricker, Maram Alokaili, Morgan Green, Sadie Heeringa, Amy M Wilstermann, Thomas M Freeland, Dinah Qutob, Amy Milsted, Ralf Jauch, Timothy J Triche, Connie M Krawczyk, Caleb P Bupp, Surender Rajasekaran, Mathias Francois, Jeremy W Prokop
Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships. Genes 14 (1) (2023)
Caleb P Bupp, Elizabeth G Ames, Madison K Arenchild, Sara Caylor, David P Dimmock, Joseph D Fakhoury, Padmani Karna, April Lehman, Cristian I Meghea, Vinod K Misra, Danielle A Nolan, Jessica O'Shea, Aditi Sharangpani, Linda S Franck, Andrea Scheurer-Monaghan
Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer. Children (Basel, Switzerland) 10 (1) (2023)
Claudia V Aniol, Jeremy W Prokop, Surender Rajasekaran, Spencer Pageau, Sydney K Elizer, Elizabeth A VanSickle, Caleb P Bupp
Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report. BMC pediatrics 23 (1) (2023)
Daniah Albokhari, Amanda Barone Pritchard, Adelyn Beil, Candace Muss, Caleb P Bupp, Dorothy K Grange, Geoffroy Delplancq, Jennifer Heeley, Melissa Zuteck, Michelle M Morrow, Paul Kuentz, Timothy Blake Palculict, Julie Elizabeth Hoover-Fong
TELO2-related syndrome (You-Hoover-Fong syndrome): Description of 14 new affected individuals and review of the literature. American journal of medical genetics. Part A (2023)
Claudia V Aniol, Jeremy W Prokop, Surender Rajasekaran, Spencer Pageau, Sydney K Elizer, Elizabeth A VanSickle, Caleb P Bupp
Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report. BMC pediatrics 23 (1) (2023)
Adam Underwood, Daniel T Rasicci, David Hinds, Jackson T Mitchell, Jacob K Zieba, Joshua Mills, Nicholas E Arnold, Taylor W Cook, Mehdi Moustaqil, Yann Gambin, Emma Sierecki, Frank Fontaine, Sophie Vanderweele, Akansha S Das, William Cvammen, Olivia Sirpilla, Xavier Soehnlen, Kristen Bricker, Maram Alokaili, Morgan Green, Sadie Heeringa, Amy M Wilstermann, Thomas M Freeland, Dinah Qutob, Amy Milsted, Ralf Jauch, Timothy J Triche, Connie M Krawczyk, Caleb P Bupp, Surender Rajasekaran, Mathias Francois, Jeremy W Prokop
Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships. Genes 14 (1) (2023)
Linda S Franck, Andrea Scheurer-Monaghan, Caleb P Bupp, Joseph D Fakhoury, Thomas J Hoffmann, Manasi Deshpandey, Madison K Arenchild, David P Dimmock
Healthcare Professionals' Attitudes toward Rapid Whole Genome Sequencing in Pediatric Acute Care. Children (Basel, Switzerland) 9 (3) (2022)
Antara Afrin, Tonia S Afshan, Elizabeth A VanSickle, Julianne Michael, Rachel L Laarman, Caleb P Bupp
Improvement of dermatological symptoms in patients with Bachmann-Bupp syndrome using difluoromethylornithine treatment. Pediatric dermatology (2022)
Konrad Platzer, Heinrich Sticht, Caleb P Bupp, Mythily Ganapathi, Elaine Maria Pereira, Gwenaël L E Guyader, Frederic Bilan, Lindsay B Henderson, Johannes R Lemke, Holger Taschenberger, Nils Brose, Rami Abou Jamra, Sonja M Wojcik
De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission. Annals of neurology 92 (6) (2022)
Jeremy W Prokop, Caleb P Bupp, Austin Frisch, Stephanie M Bilinovich, Daniel B Campbell, Daniel Vogt, Chad R Schultz, Katie L Uhl, Elizabeth VanSickle, Surender Rajasekaran, André S Bachmann
Emerging Role of ODC1 in Neurodevelopmental Disorders and Brain Development. Genes 12 (4) (2021)
Nisha Korakavi, Caleb P Bupp, Bethany Grysko, Jane Juusola, Chelsea Borta, Casey Madura
First case of pan-suture craniosynostosis due to de novo mosaic KAT6A mutation. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2021)
Silvia Kalantari, Colleen M Carlston, Norah S Alsaleh, Ghada M H Abdel-Salam, Fowzan Sami Alkuraya, Mitsuhiro Kato, Naomichi Matsumoto, Satoko Miyatake, Tatsuya Yamamoto, Lucas Fares-Taie, Jean-Michel Rozet, Nicolas Chassaing, Catherine Vincent-Delorme, Anjeung Kang-Bellin, Kirsty McWalter, Caleb P Bupp, Emily Palen, Monisa D Wagner, Marcello Niceta, Claudia Cesario, Roberta Milone, Julie Kaplan, Erin Wadman, William B Dobyns, Isabel Filges
Expanding the KIF4A-associated phenotype. American journal of medical genetics. Part A 185 (12) (2021)
Elizabeth A VanSickle, Julianne Michael, André S Bachmann, Surender Rajasekaran, Jeremy W Prokop, Ruben Kuzniecky, Floris C Hofstede, Katharina Steindl, Anita Rauch, Mark H Lipson, Caleb P Bupp
Expanding the phenotype: Four new cases and hope for treatment in Bachmann-Bupp syndrome. American journal of medical genetics. Part A 185 (11) (2021)
Jacob G Charron, Angel Hernandez, Stephanie M Bilinovich, Daniel L Vogt, Laura A Bedinger, Laurie H Seaver, Michael Williams, Seth Devries, Daniel B Campbell, Caleb P Bupp, Jeremy W Prokop
N-methyl-d-aspartate (NMDA) receptor genetics: The power of paralog homology and protein dynamics in defining dominant genetic variants. American journal of medical genetics. Part A (2021)

Caleb P Bupp.css-eqlu8i{font-size:small;padding-left:4px;} (Caleb Bupp)

Publication Activity (10 Years)

Top Topics

Top Venues

Caleb P Bupp (Caleb Bupp)