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Scheduling surgery groups considering multiple downstream resources

European journal of operational research, 2020-04, Vol.282 (2), p.741-752

2020

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Deconstructing cerebellar development cell by cell

PLoS genetics, 2020-04, Vol.16 (4), p.e1008630-e1008630

2020

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Reducing Seroma Formation and Its Sequelae After Mastectomy by Closure of the Dead Space: A Multi-center, Double-Blind Randomized Controlled Trial (SAM-Trial)

Annals of surgical oncology, 2021-05, Vol.28 (5), p.2599-2608

2021

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Emergency medical services and beyond: Addressing new challenges through a wide literature review

Computers & operations research, 2017-02, Vol.78, p.349-368

2017

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MILP models for the Dial-a-ride problem with transfers

EURO Journal on Transportation and Logistics, 2021, Vol.10, p.100037, Article 100037

2021

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Comparing population and incident data for optimal air ambulance base locations in Norway

Scandinavian journal of trauma, resuscitation and emergency medicine, 2018-05, Vol.26 (1), p.42-42, Article 42

2018

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Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

Nature genetics, 2012-03, Vol.44 (3), p.277-284

2012

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PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis

Disease models & mechanisms, 2024-02, Vol.17 (2)

2024

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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

Neurology, 2011-07, Vol.77 (1), p.62-66

2011

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A bi-level framework for heterogeneous fleet sizing of ride-hailing services considering an approximated mixed equilibrium between automated and non-automated traffic

European journal of operational research, 2024-06, Vol.315 (3), p.879-898

2024

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A mathematical programming model for optimal fleet management of electric car-sharing systems with Vehicle-to-Grid operations

Journal of cleaner production, 2022-09, Vol.368, p.133147, Article 133147

2022

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Hybrid differential evolution algorithm for the resource constrained project scheduling problem with a flexible project structure and consumption and production of resources

European journal of operational research, 2024-02, Vol.313 (1), p.92-111

2024

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Solution methods for the tray optimization problem

European journal of operational research, 2018-12, Vol.271 (3), p.1070-1084

2018

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Birth prevalence for congenital limb defects in the northern Netherlands: a 30-year population-based study

BMC musculoskeletal disorders, 2013-11, Vol.14 (1), p.323-323, Article 323

2013

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Dynamic planning for simultaneous recharging and relocation of shared electric taxies: A sequential MILP approach

Transportation research. Part C, Emerging technologies, 2021-04, Vol.125, p.102933, Article 102933

2021

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Justice and the human alarm system: The impact of exclamation points and flashing lights on the justice judgment process

Journal of experimental social psychology, 2008-03, Vol.44 (2), p.201-219

2008

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Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Cell, 1999-10, Vol.99 (2), p.143-153

1999

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Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene

Journal of investigative dermatology, 2004-10, Vol.123 (4), p.656-663

2004

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The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen

Journal of medical genetics, 2011-03, Vol.48 (3), p.160-167

2011

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Comparison of static ambulance location models

International journal of logistics systems and management, 2019, Vol.32 (3/4), p.292

2019

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Exact Formulation and Comparison Between the User Optimum and System Optimum Solution for Routing Privately Owned Automated Vehicles

IEEE transactions on intelligent transportation systems, 2019-12, Vol.20 (12), p.4567-4578

2019

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Central 22q11.2 deletions

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2707-2723

2014

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De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review

Clinical genetics, 2018-05, Vol.93 (5), p.1000-1007

2018

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Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)

Journal of medical genetics, 2010-01, Vol.47 (1), p.8-21

2010

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Scheduling Non-Urgent Patient Transportation While Maximizing Emergency Coverage

Transportation science, 2019-03, Vol.53 (2), p.492-509

2019

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Scheduling surgery groups considering multiple downstream resources

Deconstructing cerebellar development cell by cell

Reducing Seroma Formation and Its Sequelae After Mastectomy by Closure of the Dead Space: A Multi-center, Double-Blind Randomized Controlled Trial (SAM-Trial)

Emergency medical services and beyond: Addressing new challenges through a wide literature review

MILP models for the Dial-a-ride problem with transfers

Comparing population and incident data for optimal air ambulance base locations in Norway

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

PTCH1-mutant human cerebellar organoids exhibit altered neural development and recapitulate early medulloblastoma tumorigenesis

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

A bi-level framework for heterogeneous fleet sizing of ride-hailing services considering an approximated mixed equilibrium between automated and non-automated traffic

A mathematical programming model for optimal fleet management of electric car-sharing systems with Vehicle-to-Grid operations

Hybrid differential evolution algorithm for the resource constrained project scheduling problem with a flexible project structure and consumption and production of resources

Solution methods for the tray optimization problem

Birth prevalence for congenital limb defects in the northern Netherlands: a 30-year population-based study

Dynamic planning for simultaneous recharging and relocation of shared electric taxies: A sequential MILP approach

Justice and the human alarm system: The impact of exclamation points and flashing lights on the justice judgment process

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene

The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen

Comparison of static ambulance location models

Exact Formulation and Comparison Between the User Optimum and System Optimum Solution for Routing Privately Owned Automated Vehicles

Central 22q11.2 deletions

De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review

Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)

Scheduling Non-Urgent Patient Transportation While Maximizing Emergency Coverage

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