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Cell Genomics
|
August 21, 2023
Multiset correlation and factor analysis enables exploration of multi-omics data
Brielin C Brown, Collin Wang, Silva Kasela, et al.
American Journal of Human Genetics
|
April 2, 2013
Mutations in KCTD1 cause scalp-ear-nipple syndrome
Alexander G Marneros, Anita E Beck, Emily H Turner, et al.
Plos Genetics
|
March 29, 2018
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
Laura M Raffield, Jacob C Ulirsch, Rakhi P Naik, et al.
Oral Oncology
|
November 10, 2025
Integrating artificial intelligence-driven digital pathology and genomics to establish patient-derived organoids as new approach methodologies for drug response in head and neck cancer
Rose Doerfler, Jie Chen, Carl Kim, et al.
American Journal of Human Genetics
|
January 26, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2
Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, et al.
Biorxiv : the Preprint Server for Biology
|
July 16, 2025
Integrating Artificial Intelligence-Driven Digital Pathology and Genomics to Establish Patient-Derived Organoids as a Novel Alternative Model for Drug Response in Head and Neck Cancer
Rose Doerfler, Jie Chen, Carl Kim, et al.
Morbidity and Mortality Weekly Report. Surveillance Summaries (Washington, D.C. : 2002)
|
January 17, 2003
Adult blood lead epidemiology and surveillance--United States, 1998-2001
Robert J Roscoe, Wayne Ball, John J Curran, et al.
Oral Oncology
|
November 2, 2022
Prognostic value of CD103<sup>+</sup> tumor-infiltrating lymphocytes and programmed death ligand-1 (PD-L1) combined positive score in recurrent laryngeal squamous cell carcinoma
Joshua D Smith, Emily L Bellile, Susan E Ellsperman, et al.
European Journal of Human Genetics : EJHG
|
December 11, 2014
Challenges and solutions for gene identification in the presence of familial locus heterogeneity
Atteeq U Rehman, Regie Lyn P Santos-Cortez, Meghan C Drummond, et al.
JAMA
|
November 14, 2014
Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans
Rakhi P Naik, Vimal K Derebail, Morgan E Grams, et al.
Page
of 20
Search research articles
Search
Showing results (151-160 of 194) with videos related to
Sort By:
Page
of 20
Cell Genomics
|
August 21, 2023
Multiset correlation and factor analysis enables exploration of multi-omics data
Brielin C Brown, Collin Wang, Silva Kasela, et al.
American Journal of Human Genetics
|
April 2, 2013
Mutations in KCTD1 cause scalp-ear-nipple syndrome
Alexander G Marneros, Anita E Beck, Emily H Turner, et al.
Plos Genetics
|
March 29, 2018
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
Laura M Raffield, Jacob C Ulirsch, Rakhi P Naik, et al.
Oral Oncology
|
November 10, 2025
Integrating artificial intelligence-driven digital pathology and genomics to establish patient-derived organoids as new approach methodologies for drug response in head and neck cancer
Rose Doerfler, Jie Chen, Carl Kim, et al.
American Journal of Human Genetics
|
January 26, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2
Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, et al.
Biorxiv : the Preprint Server for Biology
|
July 16, 2025
Integrating Artificial Intelligence-Driven Digital Pathology and Genomics to Establish Patient-Derived Organoids as a Novel Alternative Model for Drug Response in Head and Neck Cancer
Rose Doerfler, Jie Chen, Carl Kim, et al.
Morbidity and Mortality Weekly Report. Surveillance Summaries (Washington, D.C. : 2002)
|
January 17, 2003
Adult blood lead epidemiology and surveillance--United States, 1998-2001
Robert J Roscoe, Wayne Ball, John J Curran, et al.
Oral Oncology
|
November 2, 2022
Prognostic value of CD103<sup>+</sup> tumor-infiltrating lymphocytes and programmed death ligand-1 (PD-L1) combined positive score in recurrent laryngeal squamous cell carcinoma
Joshua D Smith, Emily L Bellile, Susan E Ellsperman, et al.
European Journal of Human Genetics : EJHG
|
December 11, 2014
Challenges and solutions for gene identification in the presence of familial locus heterogeneity
Atteeq U Rehman, Regie Lyn P Santos-Cortez, Meghan C Drummond, et al.
JAMA
|
November 14, 2014
Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans
Rakhi P Naik, Vimal K Derebail, Morgan E Grams, et al.
Page
of 20