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Deterministic generation of a cluster state of entangled photons

Science (American Association for the Advancement of Science), 2016-10, Vol.354 (6311), p.434-437

2016

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HACER: an atlas of human active enhancers to interpret regulatory variants

Nucleic acids research, 2019-01, Vol.47 (D1), p.D106

2019

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Deterministic Writing and Control of the Dark Exciton Spin Using Single Short Optical Pulses

Physical review. X, 2015, Vol.5 (1), p.011009, Article 011009

2015

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Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases

The Journal of clinical investigation, 2022-04, Vol.132 (7)

2022

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Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease

American journal of respiratory and critical care medicine, 2015-02, Vol.191 (4), p.417-426

2015

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Short telomeres are a risk factor for idiopathic pulmonary fibrosis

Proceedings of the National Academy of Sciences - PNAS, 2008-09, Vol.105 (35), p.13051-13056

2008

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Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in females

The European respiratory journal, 2009-11, Vol.34 (5), p.1093-1099

2009

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A Novel Dyskerin ( DKC1 ) Mutation Is Associated With Familial Interstitial Pneumonia

Chest, 2014-07, Vol.146 (1), p.e1-e7

2014

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Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

The New England journal of medicine, 2007-03, Vol.356 (13), p.1317-1326

2007

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TBX4 Transcription Factor Is a Positive Feedback Regulator of Itself and Phospho-SMAD1/5

American journal of respiratory cell and molecular biology, 2021-01, Vol.64 (1), p.140-143

2021

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Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis

PLoS genetics, 2011-03, Vol.7 (3), p.e1001352-e1001352

2011

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Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension

Respiratory research, 2009-09, Vol.10 (1), p.87-87, Article 87

2009

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High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2006-09, Vol.174 (5), p.590-598

2006

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On-demand source of maximally entangled photon pairs using the biexciton-exciton radiative cascade

Physical review. B, 2017-06, Vol.95 (23), Article 235435

2017

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Coaching Olympic Athletes with Sport Psychology

Consulting psychology journal, 2019-06, Vol.71 (2), p.86-96

2019

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Mutations in PROP1 cause familial combined pituitary hormone deficiency

Nature genetics, 1998-02, Vol.18 (2), p.147-149

1998

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The Y Chromosome Regulates BMPR2 Expression via SRY: A Possible Reason "Why" Fewer Males Develop Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2018-12, Vol.198 (12), p.1581-1583

2018

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Towards supersensitive optical phase measurement using a deterministic source of entangled multiphoton states

Physical review. B, 2020-06, Vol.101 (24), p.1, Article 245406

2020

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Functional Prostacyclin Synthase Promoter Polymorphisms: Impact in Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2014-05, Vol.189 (9), p.1110-1120

2014

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Achalasia in a Young Woman Thought to Have Had an Eating Disorder

Irish medical journal, 2022-01, Vol.115 (1), p.529-529

2022

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Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

Nature genetics, 2013-06, Vol.45 (6), p.613-620

2013

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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

HGG advances, 2022-10, Vol.3 (4), p.100131-100131, Article 100131

2022

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Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network

American journal of human genetics, 2021-10, Vol.108 (10), p.1946-1963

2021

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Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial Interstitial Lung Disease

American journal of respiratory and critical care medicine, 2020-05, Vol.201 (10), p.1230-1239

2020

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Deterministic generation of a cluster state of entangled photons

HACER: an atlas of human active enhancers to interpret regulatory variants

Deterministic Writing and Control of the Dark Exciton Spin Using Single Short Optical Pulses

Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases

Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease

Short telomeres are a risk factor for idiopathic pulmonary fibrosis

Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in females

A Novel Dyskerin ( DKC1 ) Mutation Is Associated With Familial Interstitial Pneumonia

Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

TBX4 Transcription Factor Is a Positive Feedback Regulator of Itself and Phospho-SMAD1/5

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis

Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension

High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension

On-demand source of maximally entangled photon pairs using the biexciton-exciton radiative cascade

Coaching Olympic Athletes with Sport Psychology

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

The Y Chromosome Regulates BMPR2 Expression via SRY: A Possible Reason "Why" Fewer Males Develop Pulmonary Arterial Hypertension

Towards supersensitive optical phase measurement using a deterministic source of entangled multiphoton states

Functional Prostacyclin Synthase Promoter Polymorphisms: Impact in Pulmonary Arterial Hypertension

Achalasia in a Young Woman Thought to Have Had an Eating Disorder

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network

Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial Interstitial Lung Disease

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