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Twitter's glass ceiling: The effect of perceived gender on online visibility
S Nilizadeh, A Groggel, P Lista, S Das, YY Ahn, A Kapadia, F Rojas
Proceedings of the International AAAI Conference on Web and Social Media 10 (1), 2016
372016
Was my message read? privacy and signaling on Facebook messenger
R Hoyle, S Das, A Kapadia, AJ Lee, K Vaniea
Proceedings of the 2017 CHI Conference on Human Factors in Computing Systems …, 2017
322017
Viewing the Viewers: Publishers' Desires and Viewers' Privacy Concerns in Social Networks
R Hoyle, S Das, A Kapadia, AJ Lee, K Vaniea
Proceedings of the 2017 ACM Conference on Computer Supported Cooperative …, 2017
142017
Fitted q-learning for relational domains
S Das, S Natarajan, K Roy, R Parr, K Kersting
arXiv preprint arXiv:2006.05595, 2020
52020
On Whom Should I Perform this Lab Test Next? An Active Feature Elicitation Approach.
S Natarajan, S Das, N Ramanan, G Kunapuli, P Radivojac
IJCAI, 3498-3505, 2018
42018
Prenatal diagnostic conundrum involving a novel ATP7A duplication
C Schoonveld, A Donsante, D Del Gaudio, D Waggoner, S Das, SG Kaler
Clinical genetics 84 (1), 97, 2013
22013
A clustering based selection framework for cost aware and test-time feature elicitation
S Das, R Iyer, S Natarajan
8th ACM IKDD CODS and 26th COMAD, 20-28, 2021
12021
Measurement of the inclusive jet cross section in pp collisions at s?= 2.76 TeV
CMS Collaboration, V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, ...
European Physical Journal C 76 (5), 2016
12016
Development of a genomic DNA reference material panel for rett syndrome genetic testing
L Kalman, J Tarleton, A Percy, S Aradhya, S Bale, P Bayrak-Toydemir, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 15 (6), 845-846, 2013
12013
Sample Efficient Cost-Aware Active Learning
S Das
PQDT-Global, 2020
2020
Cost Aware Feature Elicitation.
S Das, R Iyer, S Natarajan
KiML@ KDD, 23-29, 2020
2020
Improved Diagnosis for Familial Myelodysplastic Syndromes and Acute Leukemia Using Next-generation Sequencing and Splicing Analysis
L Guidugli, AK Johnson, G Alkorta-Aranburu, V Nelakuditi, K Arndt, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 17 (6), 772-772, 2015
2015
Development of Consensus Reference Material Tools for Clinical Next-Generation Sequencing Tests
D Church, B Funke, M Hegde, C Chao, J Trow, D Slotta, M Halavi, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 15 (6), 847-847, 2013
2013
P2. 81 Further delineation of FOXG1-associated encephalopathy
G Uyanik, F Kortüm, S Das, M Flindt, DJ Morris-Rosendahl, D Horn
International Journal of Developmental Neuroscience 28 (8), 715, 2010
2010
Erratum: Technical standards and guidelines: Molecular genetic testing for ultra-rare disorders (Genetics in Medicine (2005) 8,(571-583))
A Maddalena, S Bale, S Das, W Grody, CS Richards
Genetics in Medicine 8 (11), 735, 2006
2006
Prenatal diagnosis of paternal uniparental disomy 14.
P Rush, M Quigg, J Refuerzo, J Roberson, S Das, D Van Dyke
GENETICS IN MEDICINE 6 (4), 368-368, 2004
2004
Severe growth retardation and limb anomalies in a boy with 47, XY,+ r (7) and maternal uniparental disomy for chromosome 7
CS Stadter, J Stamberg, S Das, EA Wulfsberg
Genetics in Medicine 2 (1), 95-95, 2000
2000
Reference:“Guidelines of the American College of Medical Genetics and Genomics (ACMG)“
S Richards, N Aziz, S Bale, D Bick, S Das, J Gastier-Foster
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