Sara Halbach

846 total citations
6 papers, 97 citations indexed

About

Sara Halbach is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Sara Halbach has authored 6 papers receiving a total of 97 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Sara Halbach's work include Genomic variations and chromosomal abnormalities (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Sara Halbach is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Sara Halbach collaborates with scholars based in United States, Finland and Netherlands. Sara Halbach's co-authors include Darrel Waggoner, Elaine H. Zackai, Donna M. McDonald‐McGinn, Elizabeth Bhoj, Christopher Tan, Laura Russell, Nicole Revençu, Laurence M. Boon, Håkon Håkonarson and Chad Haldeman‐Englert and has published in prestigious journals such as American Journal of Medical Genetics Part A, Neurogenetics and Genes & Diseases.

In The Last Decade

Sara Halbach

6 papers receiving 93 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sara Halbach United States	5	47	44	26	12	12	6	97
Resham Ejaz Canada	7	42 0.9×	55 1.3×	17 0.7×	12 1.0×	13 1.1×	16	132
Edith Said Malta	8	44 0.9×	67 1.5×	23 0.9×	9 0.8×	4 0.3×	13	122
François Lecoquierre France	7	57 1.2×	63 1.4×	13 0.5×	10 0.8×	3 0.3×	18	114
Lucile Pinson France	6	34 0.7×	68 1.5×	12 0.5×	7 0.6×	32 2.7×	8	116
August Allocco United States	6	22 0.5×	23 0.5×	8 0.3×	8 0.7×	10 0.8×	6	72
Birgitta Bernhard United Kingdom	7	57 1.2×	58 1.3×	7 0.3×	10 0.8×	6 0.5×	10	114
Laura S. Farach United States	7	57 1.2×	71 1.6×	5 0.2×	7 0.6×	4 0.3×	22	127
Zhanying Dong China	5	30 0.6×	69 1.6×	6 0.2×	7 0.6×	8 0.7×	7	113
Aziz Mhanni Canada	6	54 1.1×	50 1.1×	14 0.5×	5 0.4×	7 0.6×	10	102
Shivarajan Amudhavalli United States	8	62 1.3×	67 1.5×	16 0.6×	5 0.4×	6 0.5×	12	125

Countries citing papers authored by Sara Halbach

Since Specialization

Citations

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

Fields of papers citing papers by Sara Halbach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Halbach

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

All Works

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6 of 6 papers shown

1.

Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations

2.

Lyon, Sarah, Darrel Waggoner, Sara Halbach, et al.. (2015). Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2. Genes & Diseases. 2(4). 347–352. 7 indexed citations

3.

Halbach, Sara, et al.. (2015). 4q21 microdeletion in a patient with epilepsy and brain malformations. American Journal of Medical Genetics Part A. 167(6). 1409–1413. 2 indexed citations

4.

Bhoj, Elizabeth, Sara Halbach, Donna M. McDonald‐McGinn, et al.. (2013). Expanding the spectrum of microdeletion 4q21 syndrome: A partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and pierre robin sequence. American Journal of Medical Genetics Part A. 161(9). 2327–2333. 19 indexed citations

5.

Revençu, Nicole, Laurence M. Boon, A. Dompmartin, et al.. (2013). Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. Molecular Syndromology. 4(4). 173–178. 29 indexed citations

6.

Haldeman‐Englert, Chad, Xiaowu Gai, Juan C. Perín, et al.. (2008). A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay. European Journal of Medical Genetics. 52(4). 265–268. 15 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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