Sally A. Camper - Publications, H-index & Citations

Sally A. Camper

University of Michigan Medical School

74H指数

322论文数

1.7W被引数

收录论文 69

发表时间

Compound Heterozygous Variants in the Phospholipase Gene PNPLA6 Cause Hypopituitarism and Vision Loss PNPLA6磷脂酶基因复合杂合变异导致垂体功能减退和视力丧失

Human Mutation

IF3.7

2026-06-19

OAAI

Sebastian Vishnopolska; James Liu; Maria Andrea Camilletti; Julian Martinez Mayer; Lucia Iglesias Garcia; Michelle Brinkmeier; Elisa Vaiani; Sofia Hebe Vidal; Marta Ciaccio; María Isabel Di Palma; Alicia Belgorosky; Marcelo Marti; Robert B. Hufnagel; Sally A. Camper; Maria Ines Perez-Millan

NR3C1 is required for normal somatotrope differentiation and Foxo1 expression in pituitary NR3C1对于垂体生长素细胞正常分化和Foxo1表达是必需的

Endocrinology

IF3.3

2026-05-16

OAAI

Pratyusa Das; Ridwanullah A Abubakar; Nooshin Mojahed; Dania Abou-Jabal; Prisha Kittu; Michelle L Brinkmeier; Jessica Olsen; Dale Ann Sunny; Sally A Camper; Robin Lovell-Badge; Karine Rizzoti; Buffy S Ellsworth; null

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation

HUMAN MOLECULAR GENETICS

IF3.2

2025-03-01

OAAI

Brinkmeier, Michelle L.; Cheung, Leonard Y. M.; O'Connell, Sean P.; Gutierrez, Diana K.; Rhoads, Eve C.; Camper, Sally A.; Davis, Shannon W.

Long Noncoding RNAs Expressed in Mouse Pituitary Development and Mature Hormone-Producing Cells 在小鼠垂体发育和成熟激素产生细胞中表达的长链非编码rna

ENDOCRINOLOGY

IF3.3

2024-11-02

OAAI

Brinkmeier, Michelle Lynn; George, Akima Semone; Cheung, Leonard Yan Ming; Mills, Ryan Edward; Melamed, Philippa; Camper, Sally Ann

Ash1l loss-of-function results in structural birth defects and altered cortical development Ash1l功能丧失导致结构性出生缺陷和皮质发育改变

BRAIN

IF11.7

2024-06-30

PREAI

Toolan, Kevin P.; McGrath, Brian T.; Brinkmeier, Michelle L.; Camper, Sally A.; Bielas, Stephanie L.

Pituitary stem cells: past, present and future perspectives 垂体干细胞: 过去，现在和未来的观点

nature reviews endocrinology

IF40

2023-12-15

OAAI

Millan, Maria Ines Perez; Cheung, Leonard Y. M.; Mercogliano, Florencia; Camilletti, Maria Andrea; Felker, Gonzalo T. Chirino; Moro, Lucia N.; Miriuka, Santiago; Brinkmeier, Michelle L.; Camper, Sally A.

Novel Candidate Regulators and Developmental Trajectory of Pituitary Thyrotropes

ENDOCRINOLOGY

IF3.3

2023-05-15

PREAI

Cheung, Leonard Y. M.; Menage, Lucy; Rizzoti, Karine; Hamilton, Greg; Dumontet, Typhanie; Basham, Kaitlin; Daly, Alexandre Z.; Brinkmeier, Michelle L.; Masser, Bailey E.; Treier, Mathias; Cobb, John; Delogu, Alessio; Lovell-Badge, Robin; Hammer, Gary D.; Camper, Sally A.

Disruption of RNA Splicing Is an Important Contributor to Congenital Hypopituitarism and Other Human Genetic Diseases RNA剪接的破坏是先天性垂体功能减退症和其他人类遗传疾病的重要原因

ENDOCRINOLOGY

IF3.3

2023-03-01

OAAI

Camper, Sally A.; Smith, Cathy; Kitzman, Jacob O.

Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling Zeb2和BMP信号对垂体干细胞的调控

ENDOCRINOLOGY

IF3.3

2023-01-23

OAAI

Winningham, Amanda H.; Camper, Sally A.

Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2022-09-27

OAAI

Bando, Hironori; Urai, Shin; Kanie, Keitaro; Sasaki, Yuriko; Yamamoto, Masaaki; Fukuoka, Hidenori; Iguchi, Genzo; Camper, Sally A.

Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man SIX3和POU1F1的杂合变异导致小鼠和人的垂体激素缺乏

HUMAN MOLECULAR GENETICS

IF3.2

2022-08-11

OAAI

Bando, Hironori; Brinkmeier, Michelle L.; Castinetti, Frederic; Fang, Qing; Lee, Mi-Sun; Saveanu, Alexandru; Albarel, Frederique; Dupuis, Clementine; Brue, Thierry; Camper, Sally A.

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2021-08-01

OAAI

Gergics, Peter; Smith, Cathy; Bando, Hironori; Jorge, Alexander A. L.; Rockstroh-Lippold, Denise; Vishnopolska, Sebastian A.; Castinetti, Frederic; Maksutova, Mariam; Silveira Carvalho, Luciani Renata; Hoppmann, Julia; Mayer, Julian Martinez; Albarel, Frederique; Braslavsky, Debora; Keselman, Ana; Bergada, Ignacio; Marti, Marcelo A.; Saveanu, Alexandru; Barlier, Anne; Abou Jamra, Rami; Guo, Michael H.; Dauber, Andrew; Nakaguma, Marilena; Mendonca, Berenice B.; Jayakody, Sajini N.; Ozel, A. Bilge; Fang, Qing; Ma, Qianyi; Li, Jun Z.; Brue, Thierry; Millan, Maria Ines Perez; Arnhold, Ivo J. P.; Pfaeffle, Roland; Kitzman, Jacob O.; Camper, Sally A.

The phenotypic spectrum associated with OTX2 mutations in humans

EUROPEAN JOURNAL OF ENDOCRINOLOGY

IF5.2

2021-07-01

OAAI

Gregory, Louise C.; Gergics, Peter; Nakaguma, Marilena; Bando, Hironori; Patti, Giuseppa; McCabe, Mark J.; Fang, Qing; Ma, Qianyi; Ozel, Ayse Bilge; Li, Jun Z.; Poina, Michele Moreira; Jorge, Alexander A. L.; Benedetti, Anna F. Figueredo; Lerario, Antonio M.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Maghnie, Mohamad; Camper, Sally A.; Carvalho, Luciani R. S.; Dattani, Mehul T.

Pituitary Tumors and Immortalized Cell Lines Generated by Cre-Inducible Expression of SV40 T Antigen Cre诱导的SV40 T抗原表达产生的垂体瘤和永生化细胞系

ENDOCRINOLOGY

IF3.3

2021-04-09

OAAI

Daly, Alexandre Z.; Mortensen, Amanda H.; Bando, Hironori; Camper, Sally A.

Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans

NATURE COMMUNICATIONS

IF15.7

2021-04-01

OAAI

Gualtieri, Angelica; Kyprianou, Nikolina; Gregory, Louise C.; Vignola, Maria Lillina; Nicholson, James G.; Tan, Rachael; Inoue, Shin-ichi; Scagliotti, Valeria; Casado, Pedro; Blackburn, James; Abollo-Jimenez, Fernando; Marinelli, Eugenia; Besser, Rachael E. J.; Hoegler, Wolfgang; Temple, I. Karen; Davies, Justin H.; Gagunashvili, Andrey; Robinson, Iain C. A. F.; Camper, Sally A.; Davis, Shannon W.; Cutillas, Pedro R.; Gevers, Evelien F.; Aoki, Yoko; Dattani, Mehul T.; Gaston-Massuet, Carles

Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2021-03-17

OAAI

Vishnopolska, Sebastian Alexis; Mercogliano, Maria Florencia; Camilletti, Maria Andrea; Mortensen, Amanda Helen; Braslavsky, Debora; Keselman, Ana; Bergada, Ignacio; Olivieri, Federico; Miranda, Lucas; Marino, Roxana; Ramirez, Pablo; Garrido, Natalia Perez; Mejia, Helen Patino; Ciaccio, Marta; Di Palma, Maria Isabel; Belgorosky, Alicia; Marti, Marcelo Adrian; Kitzman, Jacob Otto; Camper, Sally Ann; Perez-Millan, Maria Ines

Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time?垂体肿瘤命名研讨会: 腺瘤经得起时间的考验吗？

JOURNAL OF THE ENDOCRINE SOCIETY

IF3.1

2021-02-09

OAAI

Ho, Ken; Fleseriu, Maria; Kaiser, Ursula; Salvatori, Roberto; Brue, Thierry; Lopes, M. Beatriz; Kunz, Pamela; Molitch, Mark; Camper, Sally A.; Gadelha, Monica; Syro, Luis, V; Laws, Edward; Reincke, Martin; Nishioka, Hiroshi; Grossman, Ashley; Barkan, Ariel; Casanueva, Felipe; Wass, John; Mamelak, Adam; Katznelson, Laurence; van der Lely, Aart J.; Radovick, Sally; Bidlingmaier, Martin; Boguszewski, Margaret; Bollerslev, Jens; Hoffman, Andrew R.; Oyesiku, Nelson; Raverot, Gerald; Ben-Shlomo, Anat; Fowkes, Rob; Shimon, Ilan; Fukuoka, Hidenori; Pereira, Alberto M.; Greenman, Yona; Heaney, Anthony P.; Gurnell, Mark; Johannsson, Gudmundur; Osamura, Robert Y.; Buchfelder, Michael; Zatelli, Maria Chiara; Korbonits, Marta; Chanson, Philippe; Biermasz, Nienke; Clemmons, David R.; Karavitaki, Niki; Bronstein, Marcello D.; Trainer, Peter; Melmed, Shlomo

Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors Rathke的裂隙样囊肿是由小鼠垂体祖细胞中Isl1缺失引起的

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2020-05-26

OAAI

Brinkmeier, Michelle L.; Bando, Hironori; Camarano, Adriana C.; Fujio, Shingo; Yoshimoto, Koji; de Souza, Flavio S. J.; Camper, Sally A.

Otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease

HUMAN MOLECULAR GENETICS

IF3.2

2020-04-09

OAAI

Bando, Hironori; Gergics, Peter; Bohnsack, Brenda L.; Toolan, Kevin P.; Richter, Catherine E.; Shavit, Jordan A.; Camper, Sally A.