Angela Lin
机构: Massachusetts General Hospital
每年引用次数
引用次数
引用: 17,179
H-指数: 68
I10-指数 : 174
出版物: 314
Cardiac abnormalities in neurofibromatosis.
Garver Kl , Lin Ae
Neurofibromatosis 1 ( 3) 146
19
1988
Maldescent of the thymus.
Gorlin Rj , Lin Ae
Pediatric pathology / affiliated with the International Paediatric Pathology Association 14 ( 1)
1994
Educating the obstetric community through a genetic newsletter.
A E Lin , B E Braddock , B Thayer , W A Miller
American Journal of Human Genetics 53 ( 6) 1366 -1367
1993
Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
B R Haddad , A E Lin , H Wyandt , A Milunsky
Journal of Medical Genetics 33 ( 12) 1045 -1047
48
1996
Tricuspid atresia in sibs.
A E Lin , L Rosti
Journal of Medical Genetics 35 ( 12) 1055 -1056
10
1998
Two additional patients representing the possible human homologue for the mouse mutant disorganisation (Ds)
A E Lin
Journal of Medical Genetics 28 ( 9) 645 -647
17
1991
Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities
J C Hodge , E Mitchell , V Pillalamarri , T L Toler
Molecular Psychiatry 19 ( 3) 368 -379
65
2014
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome (vol 49, pg 238, 2017)
A Verloes , ME Talkowski , JF Gusella , LA Schimmenti
NATURE GENETICS , 49 (6) p. 969. (2017)
1
2017
Neuroblastoma and Congenital Cardiovascular Malformations
Angela E. Lin , Luca Rosti , Alessandro Frigiola
Pediatrics 97 ( 2) 258 -261
11
1996
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Richard J. Czosek , Sulagna C. Saitta , Elaine H. Zackai , Jaya Ganesh
PMC
24
2018
Genetic counseling for women with 45,X/46,XX mosaicism: Towards more personalized management
Adrianna K. San Roman , Irene Souter , Frances J. Hayes , Angela E. Lin
European Journal of Medical Genetics 64 ( 3) 104140 -104140
1
2021
Lack of resemblance between Myhre syndrome and other "segmental progeroid" syndromes warrants restraint in applying this classification.
Bert Callewaert , Bert Callewaert , Valérie Cormier-Daire , T. Bernard Kinane
Geroscience 43 ( 2) 459 -461
2021
High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses
Eva Horemuzova , Eva Horemuzova , David Chitayat , David Chitayat
Journal of Human Genetics 1 -14
2021
Klinefelter Syndrome and Turner Syndrome.
Carole Samango-Sprouse , Andrea L. Gropman , Andrea L. Gropman , Cynthia M. Powell
Pediatrics in Review 42 ( 5) 272 -274
2021
The earliest depictions of a PIK3CA-Related Overgrowth Spectrum disorder: 17th-18th century prints of women with severe limb overgrowth.
Thomas F. Heyne , Giovanni Neri , Angela E. Lin
American Journal of Medical Genetics Part C-seminars in Medical Genetics
2021
Assisted Reproductive Technology and Birth Defects: Effects of Subfertility and Multiple Births
Rebecca F. Liberman , Kelly D. Getz , Dominique Heinke , Barbara Luke
Birth defects research 109 ( 14) 1144 -1153
24
2017
Causes of Congenital Malformations.
M. Hassan Toufaily , Marie-Noel Westgate , Angela E. Lin , Lewis B. Holmes
Birth defects research 110 ( 2) 87 -91
15
2018
The Active Malformations Surveillance Program, Boston in 1972–2012: Methodology and demographic characteristics
Lewis B. Holmes , Hanah Nasri , Marie-Noel Westgate , M. Hassan Toufaily
Birth defects research 110 ( 2) 148 -156
12
2018
Malformations Surveillance: Comparison between Findings at Birth and Age 1 Year.
Emma G. Thomas , Cathleen Higgins , Marie-Noel Westgate , Angela E. Lin
Birth defects research 110 ( 2) 142 -147
7
2018
Alternatives to Autopsy for Fetal and Early Neonatal (Perinatal) Deaths: Insights from the Wisconsin Stillbirth Service Program
Elspeth McPherson , Eirini Nestoridi , Dominique Heinke , Drucilla J. Roberts
Birth defects research 109 ( 18) 1430 -1441
11
2017