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International Journal of Cancer
|
September 13, 2016
Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2
Cornelia Kraus, Juliane Hoyer, Georgia Vasileiou, et al.
Human Genetics
|
July 19, 2024
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Elisabeth Bosch, Esther Güse, Philipp Kirchner, et al.
Nutrition in Clinical Practice : Official Publication of the American Society for Parenteral and Enteral Nutrition
|
August 20, 2019
Use of Predictive Equations for Energy Prescription Results in Inaccurate Estimation in Trauma Patients
Georgia Vasileiou, Sinong Qian, Rahul Iyengar, et al.
BMC Cancer
|
September 28, 2018
Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria
Juliane Hoyer, Georgia Vasileiou, Steffen Uebe, et al.
Journal of Neurology
|
August 22, 2016
Gender-based analysis of cortical thickness and structural connectivity in Parkinson's disease
Santosh K Yadav, Nagarajan Kathiresan, Suyash Mohan, et al.
JPEN. Journal of Parenteral and Enteral Nutrition
|
June 21, 2020
Early hypermetabolism is uncommon in trauma intensive care unit patients
Saskya Byerly, Georgia Vasileiou, Sinong Qian, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2021
Manifestation of epilepsy in a patient with EED-related overgrowth (Cohen-Gibson syndrome)
Katalin L M L Hetzelt, Martin Winterholler, Frank Kerling, et al.
Epilepsia
|
May 30, 2026
High incidence of Y-chromosome mosaicism in male and female individuals with mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy
Erica Cecchini, Till Hartlieb, Ahmed Gaballa, et al.
American Journal of Human Genetics
|
June 11, 2013
De novo mutations in the genome organizer CTCF cause intellectual disability
Anne Gregor, Martin Oti, Evelyn N Kouwenhoven, et al.
The Journal of Surgical Research
|
April 12, 2025
Comparison of Risk Assessment Tools' Prediction of Outcomes for Penetrating Trauma
Jeffrey Santos, Catherine M Kuza, Xi Luo, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 69) with videos related to
Sort By:
Page
of 7
International Journal of Cancer
|
September 13, 2016
Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2
Cornelia Kraus, Juliane Hoyer, Georgia Vasileiou, et al.
Human Genetics
|
July 19, 2024
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Elisabeth Bosch, Esther Güse, Philipp Kirchner, et al.
Nutrition in Clinical Practice : Official Publication of the American Society for Parenteral and Enteral Nutrition
|
August 20, 2019
Use of Predictive Equations for Energy Prescription Results in Inaccurate Estimation in Trauma Patients
Georgia Vasileiou, Sinong Qian, Rahul Iyengar, et al.
BMC Cancer
|
September 28, 2018
Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria
Juliane Hoyer, Georgia Vasileiou, Steffen Uebe, et al.
Journal of Neurology
|
August 22, 2016
Gender-based analysis of cortical thickness and structural connectivity in Parkinson's disease
Santosh K Yadav, Nagarajan Kathiresan, Suyash Mohan, et al.
JPEN. Journal of Parenteral and Enteral Nutrition
|
June 21, 2020
Early hypermetabolism is uncommon in trauma intensive care unit patients
Saskya Byerly, Georgia Vasileiou, Sinong Qian, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2021
Manifestation of epilepsy in a patient with EED-related overgrowth (Cohen-Gibson syndrome)
Katalin L M L Hetzelt, Martin Winterholler, Frank Kerling, et al.
Epilepsia
|
May 30, 2026
High incidence of Y-chromosome mosaicism in male and female individuals with mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy
Erica Cecchini, Till Hartlieb, Ahmed Gaballa, et al.
American Journal of Human Genetics
|
June 11, 2013
De novo mutations in the genome organizer CTCF cause intellectual disability
Anne Gregor, Martin Oti, Evelyn N Kouwenhoven, et al.
The Journal of Surgical Research
|
April 12, 2025
Comparison of Risk Assessment Tools' Prediction of Outcomes for Penetrating Trauma
Jeffrey Santos, Catherine M Kuza, Xi Luo, et al.
Page
of 7