Louanne Hudgins

Professor

Pediatrics Department, Stanford University

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Bio

Clinical Focus
Perinatal Genetics
Clinical Genetics and Genomics

Honors & Awards
Mosbacher Family Distinguished Packard Fellow, Stanford University School of Medicine, Department of Pediatrics (2008-present)

Papers160 papers

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Addendum: Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

Melanie Manning,Louanne Hudgins

Genetics in medicine : official journal of the American College of Medical Genetics, (2020)

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Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)

Himali Jayakody, Sanam Zarei, Huy Nguyen, Joline Dalton, Kelly Chen,Louanne Hudgins, John Day, Kara Withrow,Arti Pandya, Jean Teasley,William B Dobyns, Katherine D Mathews

Journal of neuropathology and experimental neurology, no. 9 (2020): 998-1010

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RASopathies: A significant cause of polyhydramnios

Rachel Mangels,Yair J Blumenfeld, Margaret Homeyer, Barbora Mrazek-Pugh,Susan R Hintz,Louanne Hudgins

Prenatal diagnosis, (2020)

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POLYHYDRAMNIOS AS A MARKER FOR FETAL GENETIC CONDITIONS

R. Mangels, M. Homeyer,Y. Blumenfeld,S. Hintz,L. Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4.0 (2020): 936.0-936

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CHARACTERIZING THE PRENATAL RENAL PHENOTYPES ASSOCIATED WITH 17Q12/HNF1B DELETIONS

F. Velez-Bartolomei, E. Bodle, K. Chan,M. Lyons, W. Thorson, W. H. Tan,E. H. Zackai, M. A. Thomas,C. Stevens,M. P. Adam,M. Jones,L. Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4.0 (2020): 935.0-935

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FURTHER CHARACTERIZATION OF CTCF AS A RARE CAUSE OF INTELLECTUAL DISABILITY

M. Manning, F. Velez-Bartolomei,S. Schelley, A. Hanson-Kahn,E. Smith,L. Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4.0 (2020): 938.0-938

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Prenatally diagnosed omphalocele: characteristics associated with adverse neonatal outcomes

Valerie Y Chock,Alexis S Davis, Seo-Ho Cho, Christina Bax, Elizabeth Fluharty, Nicole Weigel, Margaret Homeyer,Louanne Hudgins, Richard Jones,Erika Rubesova,Karl G Sylvester,Yair J Blumenfeld

Journal of perinatology : official journal of the California Perinatal Association, no. 8 (2019): 1111-1117

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A. Blackburn, N. Bekheirnia, V. C. Uma,J. A. Rosenfeld, M. N. Bainbridge, Y. Yang, P. Liu, S. Madan-Khetarpal, M. R. Delgado,L. Hudgins, I. Krantz, D. Rodriguez-Buritica

bioRxiv, pp.516856-29, (2019)

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CONGENITAL ICHTHYOSIS AND CATARACTS REPRESENT A MILD PHENOTYPE OF CHANARIN-DORFMAN SYNDROME, A POTENTIALLY TREATABLE NEUTRAL LIPID STORAGE DISORDER

L. Hudgins, G. Foskett, A. Hanson-Kahn, P. Kuu,J. Teng,K. Choate

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4 (2019): 737-737

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PERINATAL PHENOTYPE OF 1P36 DELETION SYNDROME

L. Carter,A. Battaglia,A. Cherry,M. Manning,L. M. Bird, L. Dowsett, Jr. Graham J. M.,F. Alkuraya,M. Hashem, M. B. Dinulos, S. Vallee,M. P. Adam

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4 (2019): 725-726

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A BIG, BRIGHT CLUE: PRENATAL RENAL FINDINGS IN BARDET-BIEDL SYNDROME

H. M. Byers, R. Zimmer, M. Homeyer, G. K. Foskett, A. Judy,L. Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4 (2019): 725-725

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Alexandria T. M. Blackburn, Nasim Bekheirnia, Vanessa C. Uma, Mark E. Corkins, Yuxiao Xu,Jill A. Rosenfeld,Matthew N. Bainbridge,Yaping Yang,Pengfei Liu,Suneeta Madan-Khetarpal,Mauricio R. Delgado,Louanne Hudgins

Genetics in Medicine, pp.1, (2019)

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PRENATAL ULTRASOUND FINDINGS CONSISTENT WITH NAGER SYNDROME ALLOW FOR IMPROVED PREGNANCY MANAGEMENT

Meredith Allain,Melanie Manning,Jonathan Bernstein, Greg Enns, Norah Alsaleh, Nada Derar,Louanne Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 6 (2018): 1488-1489

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17q12 DELETION: A COMMON CAUSE OF KIDNEY AND URINARY TRACT ABNORMALITIES IDENTIFIED PRENATALLY

L. Hudgins, A. Richardson, M. Homeyer,P. Grimm,Y. Blumenfeld,S. Hintz

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 6 (2018): 1499-1500

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ANORECTAL ANOMALIES IN NOONAN SYNDROME

G. K. Foskett,D. A. Stevenson, E. R. Farrelly, N. S. Alsaleh, C. P. DeFilippo,L. Hudgins, W. L. Thorson

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 6 (2018): 1507-1507

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Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

Kelly E Ormond, Miranda L G Hallquist,Adam H Buchanan, Danielle Dondanville,Mildred K Cho,Maureen Smith,Myra Roche, Kyle B Brothers,Curtis R Coughlin,Laura Hercher,Louanne Hudgins, Seema Jamal

Genetics in medicine : official journal of the American College of Medical Genetics, (2018)

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Autosomal recessive Stickler syndrome resulting from a COL9A3 mutation

Andrea Hanson-Kahn,Bing Li,Daniel H. Cohn,Deborah A. Nickerson,Michael J. Bamshad,Louanne Hudgins

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 12 (2018): 2887-2891

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181 Prenatally identified kidney and urinary tract abnormalities in 17q12 deletion

Ee Bodle, A Richardson,M Homeyer, Sr Hintz, Pc Grimm,Y Blumenfeld, C Mcdougall,E Zackai,L Hudgins

Journal of Investigative Medicine, no. 1 (2018)

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De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features

Mari J Tokita, Chun-An Chen,David Chitayat, Ellen Macnamara,Jill A Rosenfeld, Neil Hanchard, Andrea M Lewis, Chester W Brown, Ronit Marom, Yunru Shao, Danica Novacic,Lynne Wolfe

AMERICAN JOURNAL OF HUMAN GENETICS, no. 1 (2018): 154-162

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Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies

Bo Yuan, Juanita Neira,Davut Pehlivan, Teresa Santiago-Sim, Xiaofei Song,Jill Rosenfeld,Jennifer E Posey, Vipulkumar Patel, Weihong Jin, Margaret P Adam, Emma L Baple, John Dean

Genetics in medicine : official journal of the American College of Medical Genetics, (2018)

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