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Detecting subtle facial emotion recognition deficits in high-functioning Autism using dynamic stimuli of varying intensities

Neuropsychologia, 2010-07, Vol.48 (9), p.2777-2781

2010

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Clinical Features of Schwannomatosis: A Retrospective Analysis of 87 Patients

The oncologist (Dayton, Ohio), 2012-10, Vol.17 (10), p.1317-1322

2012

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A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

American journal of human genetics, 2018-08, Vol.103 (2), p.213-220

2018

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Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas

Nature genetics, 2013-03, Vol.45 (3), p.295-298

2013

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Facial Skin Coloration Affects Perceived Health of Human Faces

International journal of primatology, 2009-12, Vol.30 (6), p.845-857

2009

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Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas

The Journal of pathology, 2014-12, Vol.234 (4), p.436-440

2014

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The spatial phenotype of genotypically distinct meningiomas demonstrate potential implications of the embryology of the meninges

Oncogene, 2021-02, Vol.40 (5), p.875-884

2021

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Loss of SUFU Function in Familial Multiple Meningioma

American journal of human genetics, 2012-09, Vol.91 (3), p.520-526

2012

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Disease course of neurofibromatosis type 2: a 30-year follow-up study of 353 patients seen at a single institution

Neuro-oncology (Charlottesville, Va.), 2021-07, Vol.23 (7), p.1113-1124

2021

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Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

American journal of medical genetics. Part A, 2013-03, Vol.161A (3), p.405-416

2013

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SMARCE1 mutation screening in classification of clear cell meningiomas

Histopathology, 2017-04, Vol.70 (5), p.814-820

2017

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Effects of Menstrual Cycle Phase on Face Preferences

Archives of sexual behavior, 2008-02, Vol.37 (1), p.78-84

2008

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Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability

Cancers, 2021-08, Vol.13 (16), p.4154

2021

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Mapping the GRIF-1 Binding Domain of the Kinesin, KIF5C, Substantiates a Role for GRIF-1 as an Adaptor Protein in the Anterograde Trafficking of Cargoes

The Journal of biological chemistry, 2006-09, Vol.281 (37), p.27216-27228

2006

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Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis

Neurogenetics, 2012-05, Vol.13 (2), p.141-145

2012

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Maternal tendencies in women are associated with estrogen levels and facial femininity

Hormones and behavior, 2012, Vol.61 (1), p.12-16

2012

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SMARCE1 mutations in pediatric clear cell meningioma: case report

Journal of neurosurgery. Pediatrics, 2015-09, Vol.16 (3), p.296

2015

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Comparison of the frequency of loss‐of‐function LZTR1 variants between schwannomatosis patients and the general population

Human mutation, 2022-07, Vol.43 (7), p.919-927

2022

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Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations

Journal of clinical oncology, 2014-12, Vol.32 (36), p.4155-4161

2014

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Epithelial ovarian cancer risk: A review of the current genetic landscape

Clinical genetics, 2020-01, Vol.97 (1), p.54-63

2020

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PTCH2 is not a strong candidate gene for gorlin syndrome predisposition

Familial cancer, 2022-07, Vol.21 (3), p.343-346

2022

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Reproductive strategy, sexual development and attraction to facial characteristics

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2006-12, Vol.361 (1476), p.2143

2006

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A mechanistic mathematical model of initiation and malignant transformation in sporadic vestibular schwannoma

British journal of cancer, 2022-11, Vol.127 (10), p.1843-1857

2022

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Optimization of polygenic risk scores in BRCA1/2 pathogenic variant heterozygotes in epithelial ovarian cancer

Genetics in medicine, 2023-09, Vol.25 (9), p.100898-100898, Article 100898

2023

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Detecting subtle facial emotion recognition deficits in high-functioning Autism using dynamic stimuli of varying intensities

Clinical Features of Schwannomatosis: A Retrospective Analysis of 87 Patients

A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas

Facial Skin Coloration Affects Perceived Health of Human Faces

Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas

The spatial phenotype of genotypically distinct meningiomas demonstrate potential implications of the embryology of the meninges

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Loss of SUFU Function in Familial Multiple Meningioma

Disease course of neurofibromatosis type 2: a 30-year follow-up study of 353 patients seen at a single institution

Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

SMARCE1 mutation screening in classification of clear cell meningiomas

Effects of Menstrual Cycle Phase on Face Preferences

Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability

Mapping the GRIF-1 Binding Domain of the Kinesin, KIF5C, Substantiates a Role for GRIF-1 as an Adaptor Protein in the Anterograde Trafficking of Cargoes

Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis

Maternal tendencies in women are associated with estrogen levels and facial femininity

SMARCE1 mutations in pediatric clear cell meningioma: case report

Comparison of the frequency of loss‐of‐function LZTR1 variants between schwannomatosis patients and the general population

Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations

Epithelial ovarian cancer risk: A review of the current genetic landscape

PTCH2 is not a strong candidate gene for gorlin syndrome predisposition

Reproductive strategy, sexual development and attraction to facial characteristics

A mechanistic mathematical model of initiation and malignant transformation in sporadic vestibular schwannoma

Optimization of polygenic risk scores in BRCA1/2 pathogenic variant heterozygotes in epithelial ovarian cancer

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