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Harrison Brand

Showing results (1-10 of 87) with videos related to

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Pancreas|March 7, 2013
Variation in the γ-glutamyltransferase 1 gene and risk of chronic pancreatitisHarrison Brand, Brenda Diergaarde, Michael R O'Connell, et al.
Genetics|August 18, 2019
Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in HumansChen-Yu Wang, Harrison Brand, Natalie D Shaw, et al.
Cell Stem Cell|July 5, 2014
Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencingAdrian Veres, Bridget S Gosis, Qiurong Ding, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2022
Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic HypogonadismMaria I Stamou, Harrison Brand, Mei Wang, et al.
Prenatal Diagnosis|January 19, 2024
Improving prenatal diagnosis through standards and aggregationMichael H Duyzend, Pilar Cacheiro, Julius O B Jacobsen, et al.
European Journal of Human Genetics : EJHG|June 29, 2022
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP geneBoxun Zhao, Jill A Madden, Jasmine Lin, et al.
Neoplasia (New York, N.Y.)|November 3, 2009
Chaperone-targeting cytotoxin and endoplasmic reticulum stress-inducing drug synergize to kill cancer cellsJoseph M Backer, Arcadius V Krivoshein, Carl V Hamby, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2019
A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal RegulatorMaria Stamou, Shi-Yan Ng, Harrison Brand, et al.
American Journal of Human Genetics|June 23, 2015
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationHarrison Brand, Ryan L Collins, Carrie Hanscom, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
Pancreas|March 7, 2013
Variation in the γ-glutamyltransferase 1 gene and risk of chronic pancreatitisHarrison Brand, Brenda Diergaarde, Michael R O'Connell, et al.
Genetics|August 18, 2019
Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in HumansChen-Yu Wang, Harrison Brand, Natalie D Shaw, et al.
Cell Stem Cell|July 5, 2014
Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencingAdrian Veres, Bridget S Gosis, Qiurong Ding, et al.
The Journal of Clinical Endocrinology and Metabolism|May 16, 2022
Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic HypogonadismMaria I Stamou, Harrison Brand, Mei Wang, et al.
Prenatal Diagnosis|January 19, 2024
Improving prenatal diagnosis through standards and aggregationMichael H Duyzend, Pilar Cacheiro, Julius O B Jacobsen, et al.
European Journal of Human Genetics : EJHG|June 29, 2022
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP geneBoxun Zhao, Jill A Madden, Jasmine Lin, et al.
Neoplasia (New York, N.Y.)|November 3, 2009
Chaperone-targeting cytotoxin and endoplasmic reticulum stress-inducing drug synergize to kill cancer cellsJoseph M Backer, Arcadius V Krivoshein, Carl V Hamby, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2019
A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal RegulatorMaria Stamou, Shi-Yan Ng, Harrison Brand, et al.
American Journal of Human Genetics|June 23, 2015
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural VariationHarrison Brand, Ryan L Collins, Carrie Hanscom, et al.
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
Pageof 9