Sohnee Ahmed

659 total citations
9 papers, 132 citations indexed

About

Sohnee Ahmed is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sohnee Ahmed has authored 9 papers receiving a total of 132 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sohnee Ahmed's work include Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and BRCA gene mutations in cancer (2 papers). Sohnee Ahmed is often cited by papers focused on Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers) and BRCA gene mutations in cancer (2 papers). Sohnee Ahmed collaborates with scholars based in Canada, United States and Norway. Sohnee Ahmed's co-authors include William B. Dobyns, James W. Wheless, Mandy Ma, Alex R. Paciorkowski, Laurie E. Seltzer, Mary Bertrand, Grace Yoon, Christian R. Marshall, Lili‐Naz Hazrati and Jessie M. Cameron and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Sohnee Ahmed

6 papers receiving 131 citations

Peers

Sohnee Ahmed

MB

GENET

CMN

CN

CR

Patrícia B. S. Celestino-Soper United States

Lea K. Davis United States

Natalia Juliá‐Palacios Spain

Suonavy Khung France

Stephanie Karch Germany

Rita Teek Estonia

Lisa‐Marie Niestroj United States

Shirong Lai China

Daniel L Rice United Kingdom

Renée Carroll Australia

Patrícia B. S. Celestino-Soper United States

Sohnee Ahmed

97 ×1.3

MB

76 ×1.2

GENET

26 ×1.1

CMN

35 ×2.5

CN

9 ×0.6

CR

Citations per year, relative to Sohnee Ahmed Sohnee Ahmed (= 1×) peers Patrícia B. S. Celestino-Soper

Countries citing papers authored by Sohnee Ahmed

Since Specialization

Citations

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

Fields of papers citing papers by Sohnee Ahmed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sohnee Ahmed

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Ahmed, Sohnee, et al.. (2023). Shifts in the genetic counseling workforce highlight a need for laboratory fieldwork experience for genetic counseling trainees. Journal of Genetic Counseling. 32(6). 1194–1199.

2.

Hartley, Taila, Mark A. Tarnopolsky, David A. Dyment, et al.. (2020). Channelopathies are a frequent cause of genetic ataxias associated with cerebellar atrophy (1719). Neurology. 94(15_supplement). 1 indexed citations

3.

Hartley, Taila, Mark A. Tarnopolsky, David A. Dyment, et al.. (2020). Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Movement Disorders Clinical Practice. 7(8). 940–949. 9 indexed citations

4.

Nimmo, Graeme, Sundararajan Venkatesh, Ashutosh Pandey, et al.. (2018). Bi-allelic mutations ofLONP1encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy. Human Molecular Genetics. 28(2). 290–306. 30 indexed citations

5.

Shugar, Andrea, et al.. (2016). Risk for Patient Harm in Canadian Genetic Counseling Practice: It's Time to Consider Regulation. Journal of Genetic Counseling. 26(1). 93–104. 9 indexed citations

6.

Stray‐Pedersen, Asbjørg, Jan-Maarten Cobben, Trine Prescott, et al.. (2016). Biallelic mutations in UNC80 cause severe hypotonia, muscle weakness, growth retardation, and intellectual disability. Neuromuscular Disorders. 26. S197–S198.

7.

Stray‐Pedersen, Asbjørg, Jan-Maarten Cobben, Trine Prescott, et al.. (2015). Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. The American Journal of Human Genetics. 98(1). 202–209. 35 indexed citations

8.

Guerin, Andrea, Sohnee Ahmed, Matthew A. Deardorff, & Melissa Carter. (2015). MG-102 Coffin-siris syndrome caused by a missense mutation in arid1a. Clinical Genetics. A1.3–A2.

9.

Seltzer, Laurie E., Mandy Ma, Sohnee Ahmed, et al.. (2014). Epilepsy and outcome in FOXG1‐related disorders. Epilepsia. 55(8). 1292–1300. 48 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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