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Springer Nature4
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Human Genetics4
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20211
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Caleb Bupp results 4 · Newest (Page 1/1, per page 25)
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Genomic, transcriptomic, and protein landscape profile of CFTR and cystic fibrosisNARA Subscribed
Human Genetics · 2021 · Vol. 140 · Issue 3 · Springer
Morgan Sanders; James M. J. Lawlor; Xiaopeng Li; John N. Schuen; Susan L. Millard; Xi Zhang; Leah Buck; Bethany Grysko; Katie L. Uhl; David Hinds; Cynthia L. Stenger; Michele Morris; Neil Lamb; Hara Levy; Caleb Bupp; Jeremy W. Prokop
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Correction to: Expanding the genetic heterogeneity of intellectual disabilityNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 1 · Springer
Shams Anazi; Sateesh Maddirevula; Vincenzo Salpietro; Yasmine T. Asi; Saud Alsahli; Amal Alhashem; Hanan E. Shamseldin; Fatema AlZahrani; Nisha Patel; Niema Ibrahim; Firdous M. Abdulwahab; Mais Hashem; Nadia Alhashmi; Fathiya Al Murshedi; Adila Al Kindy; Ahmad Alshaer; Ahmed Rumayyan; Saeed Al Tala; Wesam Kurdi; Abdulaziz Alsaman; Ali Alasmari; Selina Banu; Tipu Sultan; Mohammed M. Saleh; Hisham Alkuraya; Mustafa A. Salih; Hesham Aldhalaan; Tawfeg Ben-Omran; Fatima Al Musafri; Rehab Ali; Jehan Suleiman; Brahim Tabarki; Ayman W. El-Hattab; Caleb Bupp; Majid Alfadhel; Nada Al Tassan; Dorota Monies; Stefan T. Arold; Mohamed Abouelhoda; Tammaryn Lashley; Henry Houlden; Eissa Faqeih; Fowzan S. Alkuraya
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Expanding the genetic heterogeneity of intellectual disabilityNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 11-12 · Springer
Shams Anazi; Sateesh Maddirevula; Vincenzo Salpietro; Yasmine T. Asi; Saud Alsahli; Amal Alhashem; Hanan E. Shamseldin; Fatema AlZahrani; Nisha Patel; Niema Ibrahim; Firdous M. Abdulwahab; Mais Hashem; Nadia Alhashmi; Fathiya Al Murshedi; Adila Al Kindy; Ahmad Alshaer; Ahmed Rumayyan; Saeed Al Tala; Wesam Kurdi; Abdulaziz Alsaman; Ali Alasmari; Selina Banu; Tipu Sultan; Mohammed M. Saleh; Hisham Alkuraya; Mustafa A. Salih; Hesham Aldhalaan; Tawfeg Ben-Omran; Fatima Al Musafri; Rehab Ali; Jehan Suleiman; Brahim Tabarki; Ayman W. El-Hattab; Caleb Bupp; Majid Alfadhel; Nada Al Tassan; Dorota Monies; Stefan T. Arold; Mohamed Abouelhoda; Tammaryn Lashley; Henry Houlden; Eissa Faqeih; Fowzan S. Alkuraya
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De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart diseaseNARA Subscribed
Human Genetics · 2016 · Vol. 135 · Issue 12 · Springer
Lijiang Ma; Yavuz Bayram; Heather M. McLaughlin; Megan T. Cho; Alyson Krokosky; Clesson E. Turner; Kristin Lindstrom; Caleb P. Bupp; Katey Mayberry; Weiyi Mu; Joann Bodurtha; Veronique Weinstein; Neda Zadeh; Wendy Alcaraz; Zöe Powis; Yunru Shao; Daryl A. Scott; Andrea M. Lewis; Janson J. White; Shalani N. Jhangiani; Elif Yilmaz Gulec; Seema R. Lalani; James R. Lupski; Kyle Retterer; Rhonda E. Schnur; Ingrid M. Wentzensen; Sherri Bale; Wendy K. Chung
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