Allison Schreiber

930 total citations
9 papers, 106 citations indexed

About

Allison Schreiber is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Allison Schreiber has authored 9 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Allison Schreiber's work include Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Allison Schreiber is often cited by papers focused on Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Allison Schreiber collaborates with scholars based in United States, Denmark and Germany. Allison Schreiber's co-authors include Jessica L. Mester, Rocio Moran, Jessika Johannsen, Kristina P. Sørensen, Ryan Noss, Deepali N. Shinde, Rami Abou Jamra, Tim M. Strom, Lars Kjærsgaard Hansen and Amy Shealy and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Neuromuscular Disorders.

In The Last Decade

Allison Schreiber

8 papers receiving 103 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Allison Schreiber United States	5	67	37	14	12	10	9	106
Sheila P. Gregório Brazil	8	56 0.8×	62 1.7×	23 1.6×	22 1.8×	9 0.9×	10	192
Laura G. Hendon United States	6	100 1.5×	99 2.7×	12 0.9×	13 1.1×	5 0.5×	10	183
Chloe M. Reuter United States	8	108 1.6×	49 1.3×	7 0.5×	14 1.2×	9 0.9×	22	180
Kimberly Foss United States	7	83 1.2×	54 1.5×	14 1.0×	14 1.2×	13 1.3×	11	139
Mateja Smogavec Austria	8	54 0.8×	58 1.6×	8 0.6×	15 1.3×	3 0.3×	16	149
Danielle Nolan United States	6	75 1.1×	46 1.2×	17 1.2×	23 1.9×	8 0.8×	10	129
Katie Golden‐Grant United States	5	37 0.6×	31 0.8×	5 0.4×	13 1.1×	7 0.7×	5	72
Kunal Sanghavi United States	7	64 1.0×	19 0.5×	22 1.6×	22 1.8×	8 0.8×	17	149
Liliana Fernández United States	6	87 1.3×	49 1.3×	10 0.7×	41 3.4×	7 0.7×	8	151
Thiago Peixoto Leal United States	8	64 1.0×	27 0.7×	2 0.1×	3 0.3×	9 0.9×	16	120

Countries citing papers authored by Allison Schreiber

Since Specialization

Citations

This map shows the geographic impact of Allison Schreiber'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 Allison Schreiber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Allison Schreiber more than expected).

Fields of papers citing papers by Allison Schreiber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allison Schreiber. 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 Allison Schreiber. The network helps show where Allison Schreiber may publish in the future.

Co-authorship network of co-authors of Allison Schreiber

This figure shows the co-authorship network connecting the top 25 collaborators of Allison Schreiber. A scholar is included among the top collaborators of Allison Schreiber 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 Allison Schreiber. Allison Schreiber is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Erwin, Angelika, Allison Schreiber, & Robert J. Desnick. (2024). P044: Congenital erythropoietic porphyria: Disease recurrence after hematopoietic stem cell transplantation. SHILAP Revista de lepidopterología. 2. 100921–100921.

Schreiber, Allison, et al.. (2023). Genetics evaluation outcomes of patients with pediatric hearing loss: 2008–2022 retrospective study. American Journal of Otolaryngology. 45(2). 104196–104196. 3 indexed citations

Matthews, Anne L., et al.. (2022). Perspectives on Spanish language concordant cancer genetic counseling sessions from the Spanish‐speaking population. Journal of Genetic Counseling. 32(1). 111–127. 2 indexed citations

Liao, Jun, Keith A. Coffman, Joseph Locker, et al.. (2021). Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea. Molecular Genetics & Genomic Medicine. 9(4). e1647–e1647. 4 indexed citations

Chamberlin, Adam, Deepali N. Shinde, Maja Hempel, et al.. (2017). De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities. The American Journal of Human Genetics. 101(6). 1013–1020. 43 indexed citations

Shealy, Amy, Allison Schreiber, Ryan Noss, et al.. (2017). Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care. Clinical and Translational Science. 11(1). 71–76. 10 indexed citations

Heald, Brandie, Lisa Rybicki, Jessica Marquard, et al.. (2016). Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices. npj Genomic Medicine. 1(1). 16010–16010. 28 indexed citations

Donkervoort, Sandra, Alice B. Schindler, Carolina Tesi Rocha, et al.. (2013). ‘Double trouble’: Diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia. Neuromuscular Disorders. 23(12). 955–961. 4 indexed citations

Mester, Jessica L., Allison Schreiber, & Rocio Moran. (2012). Genetic counselors: Your partners in clinical practice. Cleveland Clinic Journal of Medicine. 79(8). 560–568. 12 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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