Publications:

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: rs740601

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2

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Sex hormone-related polymorphisms in endometriosis and migraine: A narrative review.

Women'S Health (London, England)

van der Vaart, Joy-Fleur JF; Merki-Feld, Gabriele Susanne GS

Publication Date: 2022

Variant appearance in text: rs740601

PubMed Link: 35848345

Variant Present in the following documents:

• Main text
• 10.1177_17455057221111315.pdf

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Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research.

Cns Drugs

Elsayed, Nada A NA; Yamamoto, Kaila M KM; Froehlich, Tanya E TE

Publication Date: 2020-04

Variant appearance in text: rs740601

PubMed Link: 32133580

Variant Present in the following documents:

• Main text

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs740601

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry

Bonvicini, C C; Faraone, S V SV; Scassellati, C C

Publication Date: 2016-07

Variant appearance in text: rs740601

PubMed Link: 27217152

Variant Present in the following documents:

• Main text
• mp201674a.pdf

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Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study.

The Journal Of Headache And Pain

De Marchis, Maria Laura ML; Barbanti, Piero P; Palmirotta, Raffaele R; Egeo, Gabriella G; Aurilia, Cinzia C; Fofi, Luisa L; Piroso, Serena S; Ialongo, Cristiano C; Della-Morte, David D; D'Andrea, Giovanni G; Ferroni, Patrizia P; Guadagni, Fiorella F

Publication Date: 2015

Variant appearance in text: rs740601

PubMed Link: 25929431

Variant Present in the following documents:

• Main text
• 10194_2015_Article_520.pdf

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Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes.

Plos One

Hukic, Dzana Sudic DS; Frisén, Louise L; Backlund, Lena L; Lavebratt, Catharina C; Landén, Mikael M; Träskman-Bendz, Lil L; Edman, Gunnar G; Schalling, Martin M; Ösby, Urban U

Publication Date: 2013

Variant appearance in text: rs740601

PubMed Link: 23861766

Variant Present in the following documents:

• Main text
• pone.0067450.pdf

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Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development.

Translational Psychiatry

Ziermans, T T; Dumontheil, I I; Roggeman, C C; Peyrard-Janvid, M M; Matsson, H H; Kere, J J; Klingberg, T T

Publication Date: 2012-02-28

Variant appearance in text: rs740601

PubMed Link: 22832821

Variant Present in the following documents:

• Main text

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