Angela E Lin

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 25

Top Topics

Transforming Growth Factor

Spectrum Disorder

Pulmonary Arterial Hypertension

Top Venues

American journal of medical genetics. Part A

bioRxiv : the preprint server for biology

American journal of medical genetics. Part C, Seminars in medical genetics

Journal of the American Heart Association

This page only lists publications with an associated author ORCID identifier.

Publications

Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Karrie F Downing, Angela E Lin, Wendy N Nembhard, Charles E Rose, Jennifer G Andrews, Anthony Goudie, Scott E Klewer, Matthew E Oster, Sherry L Farr
Survival to Young Adulthood Among Individuals With Congenital Heart Defects and Genetic Syndromes: Congenital Heart Survey to Recognize Outcomes, Needs, and Well-Being. Journal of the American Heart Association 13 (15) (2024)
Angela E Lin, Eleanor R Scimone, Robyn Pauline Thom, Duraisamy Balaguru, T Bernard Kinane, Peter P Moschovis, Michael S Cohen, Weizhen Tan, Cole D Hague, Katelyn Dannheim, Lynne L Levitsky, Evelyn Lilly, Daniel V DiGiacomo, Kara M Masse, Sarah M Kadzielski, Claire A Zar-Kessler, Leo C Ginns, Ann M Neumeyer, Mary K Molly Colvin, Jack S Elder, Christopher P Learn, Hongmei Mou, Kathryn M Weagle, Karen A Buch, William E Butler, Kenda Alhadid, Patricia L Musolino, Sadia Sultana, Dhrubajyoti Bandyopadhyay, Otto Rapalino, Zachary S Peacock, Elizabeth L Chou, Gena Heidary, Aaron T Dorfman, Shaine Alaine Morris, James D Bergin, Jonathan H Rayment, Lisa A Schimmenti, Mark E Lindsay, null null
Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023). American journal of medical genetics. Part A (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Karrie F Downing, Angela E Lin, Wendy N Nembhard, Charles E Rose, Jennifer G Andrews, Anthony Goudie, Scott E Klewer, Matthew E Oster, Sherry L Farr
Survival to Young Adulthood Among Individuals With Congenital Heart Defects and Genetic Syndromes: Congenital Heart Survey to Recognize Outcomes, Needs, and Well-Being. Journal of the American Heart Association (2024)
Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul S Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
Stable and robust Xi and Y transcriptomes drive cell-type-specific autosomal and Xa responses in vivo and in vitro in four human cell types. bioRxiv : the preprint server for biology (2024)
Bailey A Martin-Giacalone, Angela E Lin, Sonja A Rasmussen, Russell S Kirby, Eirini Nestoridi, Rebecca F Liberman, A J Agopian, John C Carey, Janet D Cragan, Nina E Forestieri, Vinita Leedom, Aubree Boyce, Wendy N Nembhard, Monika Piccardi, Theresa Sandidge, Xiaoyi Shan, Charles J Shumate, Erin Bugenske Stallings, Roger Stevenson, Philip J Lupo
Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000-2017: A report from the National Birth Defects Prevention Network. American journal of medical genetics. Part A (2023)
Sreedhara Sangadala, Eileen M Shore, Meiqi Xu, Clemens Bergwitz, Santiago A Lozano Calderón, Angela E Lin, Scott D Boden, Frederick S Kaplan
Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein-1 (LMP-1). American journal of medical genetics. Part A (2023)
Adrianna K San Roman, Helen Skaletsky, Alexander K Godfrey, Neha V Bokil, Levi Teitz, Isani Singh, Laura V Blanton, Daniel W Bellott, Tatyana Pyntikova, Julian Lange, Natalia Koutseva, Jennifer F Hughes, Laura Brown, Sidaly Phou, Ashley Buscetta, Paul S Kruszka, Nicole Banks, Amalia Dutra, Evgenia Pak, Patricia C Lasutschinkow, Colleen Keen, Shanlee M Davis, Angela E Lin, Nicole R Tartaglia, Carole A Samango-Sprouse, Maximilian Muenke, David C Page
The human Y and inactive X chromosomes similarly modulate autosomal gene expression. bioRxiv : the preprint server for biology (2023)
Alexandra T Lucas, Angela E Lin, Andrew Cohen, William Muñoz, Kristopher T Kahle, John H Shin, Karen Buch, Inderneel Sahai, Ryan W Carroll
Atlantoaxial instability associated with ALDH18A1 mutation. American journal of medical genetics. Part A (2023)
Gerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, Christopher Learn, John C Dykes, Catherine L Mercer, Bert Callewaert, Ilse Meerschaut, Alessandro Mauro Spinelli, Irene Bruno, Matthew J Gillespie, Aaron T Dorfman, Adda Grimberg, Mark E Lindsay, Angela E Lin
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects. American journal of medical genetics. Part A 188 (5) (2022)
Sandra Hoyek, Marlene Wang, Audina M Berrocal, Ashley Wong, Emily M Place, Heather Mason-Suares, Angela E Lin, Shizuo Mukai, Nimesh A Patel
Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome. Ophthalmic genetics (2022)
Erin Falsey, Allison L Cirino, Emma Snyder, Marcie Steeves, Angela E Lin
Parenthood among individuals with Turner syndrome: results of an online survey of attitudes towards pregnancy, adoption, and surrogacy. Journal of community genetics 13 (3) (2022)
Gregory M Gheewalla, Jay Luther, Saumya Das, Jeffrey B Kreher, Eleanor R Scimone, Ashley W Wong, Mark E Lindsay, Angela E Lin
An additional patient with SMAD4-Juvenile Polyposis-Hereditary hemorrhagic telangiectasia and connective tissue abnormalities: SMAD4 loss-of-function and gain-of-function pathogenic variants result in contrasting phenotypes. American journal of medical genetics. Part A 188 (10) (2022)
Clara C Hildebrandt, Nisha Patel, John M Graham, Michael J Bamshad, Deborah A Nickerson, Janson J White, Colby T Marvin, Danny E Miller, null null, Katheryn L Grand, Pedro A Sanchez-Lara, Daniela Schweitzer, Hamad I Al-Zaidan, Zainab Al Masseri, Fowzan Sami Alkuraya, Angela E Lin
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American journal of medical genetics. Part A 185 (7) (2021)
Thomas F Heyne, Giovanni Neri, Angela E Lin
The earliest depictions of a PIK3CA-Related Overgrowth Spectrum disorder: 17th-18th century prints of women with severe limb overgrowth. American journal of medical genetics. Part C, Seminars in medical genetics 187 (2) (2021)
Angela E Lin, Chaya N Murali, Giovanni Neri
Syndromes and birth defects in art and antiquities: New perspectives on a familiar theme. American journal of medical genetics. Part C, Seminars in medical genetics 187 (2) (2021)
Dena R Matalon, David A Stevenson, Elizabeth Joyce Bhoj, Avni B Santani, Beth Keena, Meryl S Cohen, Angela E Lin, Sarah E Sheppard, Elaine H Zackai
Congenital polyvalvular disease expands the cardiac phenotype of the RASopathies. American journal of medical genetics. Part A 185 (5) (2021)
Angela E Lin, Nicola Brunetti-Pierri, Bert Callewaert, Valérie Cormier-Daire, Sofia Douzgou, T Bernard Kinane, Mark E Lindsay, Lois J Starr, null null
Lack of resemblance between Myhre syndrome and other "segmental progeroid" syndromes warrants restraint in applying this classification. GeroScience 43 (2) (2021)
Angela E Lin, Mitcheka Jalali
Depiction of ectrodactyly, sirenomelia and cyclopia in a figure by Hokusai. American journal of medical genetics. Part C, Seminars in medical genetics 187 (2) (2020)
Elizabeth I Pierpont, Susan A Berry, Angela E Lin, Jamie L Lohr, Lisa A Schimmenti, William B Dobyns
Mary Ella Mascia Pierpont: Geneticist, scientist, mentor, friend (1945-2020). American journal of medical genetics. Part A 185 (2) (2020)
Angela E Lin, Stephanie L Santoro, Frances A High, Paula Goldenberg, Iris Gutmark-Little
Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associations. American journal of medical genetics. Part C, Seminars in medical genetics 184 (1) (2019)
Angela E Lin, Siddharth K Prakash, Niels H Andersen, Mette H Viuff, Lynne L Levitsky, Michelle Rivera-Davila, Melissa L Crenshaw, Lars Hansen, Mary K Colvin, Frances J Hayes, Evelyn Lilly, Emma A Snyder, Shahla Nader-Eftekhari, Melissa B Aldrich, Ami B Bhatt, Laura M Prager, Ana Arenivas, Anne Skakkebaek, Marcie A Steeves, Jeffrey B Kreher, Claus H Gravholt
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years. American journal of medical genetics. Part A 179 (10) (2019)
Angela E Lin, Abdulrazak Alali, Lois Janelle Starr, Nidhi Shah, Anna Beavis, Elaine M Pereira, Mark E Lindsay, Susan Klugman
Gain-of-function pathogenic variants in SMAD4 are associated with neoplasia in Myhre syndrome. American journal of medical genetics. Part A 182 (2) (2019)