Andrea M. Lewis - Department of Molecular and Human Genetics, Baylor College of Medicine

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论文共 42 篇作者统计合作学者相似作者

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Barriers to a Successful Healthcare Transition for Individuals with Urea Cycle Disorders

Farah A. Ladha,Cynthia Le Mons,William J. Craigen,Pilar L. Magoulas,Ronit Marom,Andrea M. Lewis

Molecular Genetics and Metabolismno. 3 (2023)

引用1浏览0WOS引用

Parent Perspectives on Disclosing a Pediatric Neurofibromatosis Type 1 Diagnosis

Madeleine Franchi,Heather B. Radtke,Andrea M. Lewis,Irene Moss,Stacey S. Cofield,Ashley Cannon

JOURNAL OF GENETIC COUNSELING（2023）

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Gain and Loss of TASK3 Channel Function and Its Regulation by Novel Variation Cause KCNK9 Imprinting Syndrome

Cousin Margot A.,Veale Emma L.,Dsouza Nikita R.,Tripathi Swarnendu,Holden Robyn G.,Arelin Maria,Beek Geoffrey,Bekheirnia Mir Reza,Beygo Jasmin,Bhambhani Vikas,Bialer Martin,Bigoni Stefania,Boelman Cyrus,Carmichael Jenny,Courtin Thomas,Cogne Benjamin,Dabaj Ivana,Doummar Diane, Fazilleau Laura,Ferlini Alessandra,Gavrilova Ralitza H.,Graham John M.,Haack Tobias B.,Juusola Jane,Kant Sarina G.,Kayani Saima,Keren Boris,Ketteler Petra,Klöckner Chiara,Koopmann Tamara T.,Kruisselbrink Teresa M.,Kuechler Alma,Lambert Laëtitia,Latypova Xénia,Lebel Robert Roger,Leduc Magalie S.,Leonardi Emanuela,Lewis Andrea M.,Liew Wendy,Machol Keren,Mardini Samir,McWalter Kirsty,Mignot Cyril, McLaughlin Julie,Murgia Alessandra,Narayanan Vinodh,Nava Caroline,Neuser Sonja,Nizon Mathilde,Ognibene Davide,Park Joohyun,Platzer Konrad,Poirsier Céline,Radtke Maximilian,Ramsey Keri,Runke Cassandra K.,Guillen Sacoto Maria J.,Scaglia Fernando,Shinawi Marwan,Spranger Stephanie,Tan Ee Shien,Taylor John,Trentesaux Anne-Sophie,Vairo Filippo,Willaert Rebecca,Zadeh Neda,Urrutia Raul,Babovic-Vuksanovic Dusica,Zimmermann Michael T.,Mathie Alistair,Klee Eric W.

Genome medicine（2022）

引用6浏览0WOS引用

Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotype

Linda Z. Rossetti,Mir Reza Bekheirnia,Andrea M. Lewis,Heather C. Mefford,Katie Golden-Grant,Kristina Tarczy-Hornoch,Lauren C. Briere,David A. Sweetser,Melissa A. Walker,Elijah Kravets,David A. Stevenson, Georgette Bruenner,Jessica Sebastian, Julia Knapo,Jill A. Rosenfeld,Paul C. Marcogliese,Michael F. Wangler

Molecular genetics & genomic medicine（2021）

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Intraperitoneal Bladder Rupture in a Young Child with Vascular Ehlers-Danlos Syndrome

Rahul Nanduri,Eric Jones,Wanda Miller-Hance,Andrea M. Lewis,Shaine A. Morris

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2021）

引用14浏览0引用

Parental Perceptions of Genetic Testing for Children with Autism Spectrum Disorders

Heather M. Lucas,Andrea M. Lewis,Philip J. Lupo,Christian P. Schaaf

American journal of medical genetics Part A（2021）

引用2浏览0WOS引用

Outcomes of Prior Authorization Requests for Genetic Testing in Outpatient Pediatric Genetics Clinics

Hadley Stevens Smith,Rachel Franciskovich,Andrea M. Lewis,Amanda Gerard,Rebecca O. Littlejohn,Kimberly Nugent, Janah Rodriguez,Haley Streff

Genetics in Medicine（2021）

引用10浏览0WOS引用

Abstract 53: Missense Pathogenic Variants in ANO1 Predispose to Moyamoya Disease

Amelie Pinard,Mu He,Jill A. Rosenfeld,Wenlei Ye,Stephanie Guey,Scott Hickey,Andrea M. Lewis,Alana C. Cecchi,Dongchuan Guo,Chaker Aloui,Michael J. Bamshad,Deborah A. Nickerson,Elisabeth Tournier-Lasserve,Dianna M. Milewicz

Stroke（2020）

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