Annice Hill

457 total citations
10 papers, 253 citations indexed

About

Annice Hill is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Annice Hill has authored 10 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in Annice Hill's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Annice Hill is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Annice Hill collaborates with scholars based in United States and Kosovo. Annice Hill's co-authors include Daniel E. Hale, Jannine D. Cody, Courtney Sebold, Bridgette Soileau, Louise O’Donnell, Patricia Heard, Jack L. Lancaster, Brian P. Perry, Erika Carter and Peter T. Fox and has published in prestigious journals such as Human Genetics, Otology & Neurotology and American Journal of Medical Genetics Part C Seminars in Medical Genetics.

In The Last Decade

Annice Hill

10 papers receiving 217 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Annice Hill United States	7	212	108	69	49	17	10	253
Erika Carter United States	10	268 1.3×	118 1.1×	82 1.2×	54 1.1×	15 0.9×	15	338
Patricia A. Eng United States	5	243 1.1×	134 1.2×	104 1.5×	49 1.0×	12 0.7×	5	298
Magdalena Bartnik Poland	10	168 0.8×	140 1.3×	56 0.8×	37 0.8×	13 0.8×	23	266
Olga Žilina Estonia	12	242 1.1×	132 1.2×	92 1.3×	54 1.1×	19 1.1×	23	314
Mariana Moysés‐Oliveira Brazil	11	206 1.0×	130 1.2×	53 0.8×	35 0.7×	17 1.0×	45	300
Rosetta Lecce Italy	9	243 1.1×	175 1.6×	87 1.3×	99 2.0×	18 1.1×	11	318
Vera Ayres Meloni Brazil	9	233 1.1×	122 1.1×	59 0.9×	50 1.0×	13 0.8×	26	272
Caron D. Glotzbach United States	11	244 1.2×	137 1.3×	52 0.8×	102 2.1×	20 1.2×	11	312
Molly B. Sheridan United States	8	137 0.6×	118 1.1×	30 0.4×	34 0.7×	13 0.8×	11	281
Bridgette Soileau United States	11	345 1.6×	165 1.5×	102 1.5×	71 1.4×	18 1.1×	16	408

Countries citing papers authored by Annice Hill

Since Specialization

Citations

This map shows the geographic impact of Annice Hill's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Annice Hill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Annice Hill more than expected).

Fields of papers citing papers by Annice Hill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Annice Hill. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Annice Hill. The network helps show where Annice Hill may publish in the future.

Co-authorship network of co-authors of Annice Hill

This figure shows the co-authorship network connecting the top 25 collaborators of Annice Hill. A scholar is included among the top collaborators of Annice Hill based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Annice Hill. Annice Hill is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Moreira, Alvaro, Bridgette Soileau, Annice Hill, et al.. (2019). Abnormal bone mineral content and density in people with tetrasomy 18p. American Journal of Medical Genetics Part A. 179(3). 417–422. 1 indexed citations

Cody, Jannine D., et al.. (2018). Chromosome 18 gene dosage map 2.0. Human Genetics. 137(11-12). 961–970. 6 indexed citations

Cody, Jannine D., Patricia Heard, Annice Hill, et al.. (2018). The Chromosome 18 Clinical Resource Center. Molecular Genetics & Genomic Medicine. 6(3). 416–421. 3 indexed citations

Sebold, Courtney, Patricia Heard, Erika Carter, et al.. (2015). A review of 18p deletions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(3). 251–264. 57 indexed citations

Cody, Jannine D., Courtney Sebold, Patricia Heard, et al.. (2015). Consequences of chromsome18q deletions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(3). 265–280. 46 indexed citations

Perry, Brian P., Courtney Sebold, Patricia Heard, et al.. (2014). Sensorineural Hearing Loss in People With Deletions of 18q. Otology & Neurotology. 35(5). 782–786. 7 indexed citations

Soileau, Bridgette, Courtney Sebold, Annice Hill, et al.. (2014). Adults with Chromosome 18 Abnormalities. Journal of Genetic Counseling. 24(4). 663–674. 8 indexed citations

Soileau, Bridgette, Courtney Sebold, Annice Hill, et al.. (2011). The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions. Human Genetics. 130(6). 777–787. 32 indexed citations

Sebold, Courtney, Elizabeth Roeder, Bridgette Soileau, et al.. (2010). Tetrasomy 18p: Report of the molecular and clinical findings of 43 individuals. American Journal of Medical Genetics Part A. 152A(9). 2164–2172. 50 indexed citations

10.

Cody, Jannine D., Patricia Heard, John Li, et al.. (2009). Narrowing critical regions and determining penetrance for selected 18q‐ phenotypes. American Journal of Medical Genetics Part A. 149A(7). 1421–1430. 43 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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