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Pseudoinverse of the Laplacian and best spreader node in a network

Physical review. E, 2017-09, Vol.96 (3-1), p.032311-032311, Article 032311

2017

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Unified mean-field framework for susceptible-infected-susceptible epidemics on networks, based on graph partitioning and the isoperimetric inequality

Physical review. E, 2017-11, Vol.96 (5-1), p.052314-052314, Article 052314

2017

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Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

Clinical genetics, 2017-08, Vol.92 (2), p.166-171

2017

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Analysis of trap-assisted tunneling in vertical Si homo-junction and SiGe hetero-junction Tunnel-FETs

Solid-state electronics, 2013-05, Vol.83, p.50-55

2013

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Clinical implementation of NIPT - technical and biological challenges

Clinical genetics, 2016-05, Vol.89 (5), p.523-530

2016

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Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations

American journal of neuroradiology : AJNR, 2013-06, Vol.34 (6), p.1257-1263

2013

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Strained Germanium Gate-All-Around pMOS Device Demonstration Using Selective Wire Release Etch Prior to Replacement Metal Gate Deposition

IEEE transactions on electron devices, 2017-11, Vol.64 (11), p.4587-4593

2017

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A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome

Journal of dental research, 2017-11, Vol.96 (12), p.1386-1391

2017

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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients

European heart journal, 2007-11, Vol.28 (22), p.2778-2784

2007

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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

Journal of medical genetics, 2006-08, Vol.43 (8), p.625-633

2006

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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Journal of medical genetics, 2009-04, Vol.46 (4), p.223-232

2009

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Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects

Cytogenetic and genome research, 2011-01, Vol.135 (3-4), p.251-259

2011

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Do moose redistribute nutrients in low-productive fen systems?

Agriculture, ecosystems & environment, 2016-10, Vol.234, p.40-47

2016

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Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia

Prenatal diagnosis, 2013-12, Vol.33 (13), p.1283-1292

2013

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Pierre Robin sequence: Management of respiratory and feeding complications during the first year of life in a tertiary referral centre

International journal of pediatric otorhinolaryngology, 2015-08, Vol.79 (8), p.1206-1212

2015

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Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1

Human molecular genetics, 2013-02, Vol.22 (4), p.696-703

2013

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3-D Sequential Stacked Planar Devices Featuring Low-Temperature Replacement Metal Gate Junctionless Top Devices With Improved Reliability

IEEE transactions on electron devices, 2018-11, Vol.65 (11), p.5165-5171

2018

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Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia

European journal of medical genetics, 2014-09, Vol.57 (9), p.487-493

2014

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The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing

Clinical genetics, 2014-09, Vol.86 (3), p.207-216

2014

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Aetiology of congenital hearing loss: A cohort review of 569 subjects

International journal of pediatric otorhinolaryngology, 2013-09, Vol.77 (9), p.1385-1391

2013

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Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update

Journal of intellectual disability research, 2007-09, Vol.51 (9), p.666-670

2007

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A Balanced Translocation t(6;14)(q25.3;q13.2) Leading to Reciprocal Fusion Transcripts in a Patient with Intellectual Disability and Agenesis of Corpus Callosum

Cytogenetic and genome research, 2011-01, Vol.132 (3), p.135-143

2011

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Facial Characteristics and Olfactory Dysfunction: Two Endophenotypes Related to Nonsyndromic Cleft Lip and/or Palate

BioMed research international, 2015-01, Vol.2015, p.863429-8

2015

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Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

Journal of medical genetics, 2008-02, Vol.45 (2), p.71-80

2008

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The annual incidence of DiGeorge/velocardiofacial syndrome

Journal of medical genetics, 1998-09, Vol.35 (9), p.789-790

1998

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Pseudoinverse of the Laplacian and best spreader node in a network

Unified mean-field framework for susceptible-infected-susceptible epidemics on networks, based on graph partitioning and the isoperimetric inequality

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

Analysis of trap-assisted tunneling in vertical Si homo-junction and SiGe hetero-junction Tunnel-FETs

Clinical implementation of NIPT - technical and biological challenges

Spectrum of temporal bone abnormalities in patients with Waardenburg syndrome and SOX10 mutations

Strained Germanium Gate-All-Around pMOS Device Demonstration Using Selective Wire Release Etch Prior to Replacement Metal Gate Deposition

A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects

Do moose redistribute nutrients in low-productive fen systems?

Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia

Pierre Robin sequence: Management of respiratory and feeding complications during the first year of life in a tertiary referral centre

Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1

3-D Sequential Stacked Planar Devices Featuring Low-Temperature Replacement Metal Gate Junctionless Top Devices With Improved Reliability

Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing

Aetiology of congenital hearing loss: A cohort review of 569 subjects

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update

A Balanced Translocation t(6;14)(q25.3;q13.2) Leading to Reciprocal Fusion Transcripts in a Patient with Intellectual Disability and Agenesis of Corpus Callosum

Facial Characteristics and Olfactory Dysfunction: Two Endophenotypes Related to Nonsyndromic Cleft Lip and/or Palate

Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

The annual incidence of DiGeorge/velocardiofacial syndrome

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