Christopher J Lelliott
21PUBLICATIONS
150CO-AUTHORS
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Publications (21)
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|Oct 14, 2022
Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.Stephan C Collins, Valerie E Vancollie, Anna Mikhaleva
|Mar 17, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.Lettie E Rawlins, Hashem Almousa, Shazia Khan
|May 06, 2021
Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease.Scott E Youlten, John P Kemp, John G Logan
|Jan 21, 2021
Accelerating functional gene discovery in osteoarthritis.Natalie C Butterfield, Katherine F Curry, Julia Steinberg
|Dec 28, 2020
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.Anna L Swan, Christine Schütt, Jan Rozman
|Sep 03, 2020
Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity.Zhengzheng S Liang, Irene Cimino, Binnaz Yalcin
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Frequent Collaborators
7 joint publications
Valerie E Vancollie
6 joint publications
Graham R Williams
5 joint publications
Scott E Youlten
5 joint publications
Martin Hrabe de Angelis
5 joint publications
J H Duncan Bassett
5 joint publications
Binnaz Yalcin
4 joint publications
Yann Herault
4 joint publications
K C Kent Lloyd
4 joint publications
David J Adams
3 joint publications
Paul Flicek
